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REVIEW article

Front. Pharmacol., 31 July 2020
Sec. Ethnopharmacology

Traditional Herbal Medicine in Mesoamerica: Toward Its Evidence Base for Improving Universal Health Coverage

  • 1Department of Biomedical Sciences, University of Cagliari, Cagliari, Italy
  • 2Biovision – Foundation for Ecological Development, Zurich, Switzerland
  • 3Botanical Garden, Institute of Biology, Universidad Nacional Autónoma de México, Mexico City, Mexico
  • 4Centro de Estudios en Salud, Universidad del Valle de Guatemala, Guatemala, Guatemala
  • 5Department of Epidemiology and Public Heath, Swiss TPH, University of Basel, Basel, Switzerland
  • 6Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy
  • 7Pharmacognosy and Phytotherapy, UCL School of Pharmacy, London, United Kingdom

The quality of health care in Mesoamerica is influenced by its rich cultural diversity and characterized by social inequalities. Especially indigenous and rural communities confront diverse barriers to accessing formal health services, leading to often conflicting plurimedical systems. Fostering integrative medicine is a fundamental pillar for achieving universal health coverage (UHC) for marginalized populations. Recent developments toward health sovereignty in the region are concerned with assessing the role of traditional medicines, and particularly herbal medicines, to foster accessible and culturally pertinent healthcare provision models. In Mesoamerica, as in most regions of the world, a wealth of information on traditional and complementary medicine has been recorded. Yet these data are often scattered, making it difficult for policy makers to regulate and integrate traditionally used botanical products into primary health care. This critical review is based on a quantitative analysis of 28 survey papers focusing on the traditional use of botanical drugs in Mesoamerica used for the compilation of the “Mesoamerican Medicinal Plant Database” (MAMPDB), which includes a total of 12,537 use-records for 2188 plant taxa. Our approach presents a fundamental step toward UHC by presenting a pharmacological and toxicological review of the cross-culturally salient plant taxa and associated botanical drugs used in traditional medicine in Mesoamerica. Especially for native herbal drugs, data about safety and effectiveness are limited. Commonly used cross-culturally salient botanical drugs, which are considered safe but for which data on effectiveness is lacking constitute ideal candidates for treatment outcome studies.

Introduction

Access to adequate medical care is a basic human right (Article 25, Universal Declaration of Human Rights) and universal health coverage (UHC) is core to achieving Sustainable Development Goal three (SDG 3) of the UN Agenda 2030 (UN General Assembly, 1948; UN General Assembly, 2015). The World Health Organization (WHO, 2013) highlighted the need for integrating traditional and complementary medicine (T&CM) in national health systems in order to achieve UHC while respecting consumers’ choice. A comprehensive knowledge base is fundamental for establishing policies that allow people to “access T&CM in a safe, respectful, cost-efficient and effective manner” (WHO, 2013, p. 7). Lack of research data is seen as the number one challenge faced by member states for implementing the WHO’s T&CM strategy. The lack of systematic reviews of the available evidence on T&CM in Mesoamerica is reflected in insufficient policies and culturally sensitive health materials, representing critical barriers to care (Lozoya and Zolla, 1984; Nigenda et al., 2001; WHO, 2005; Caceres Guido et al., 2015; Mokdad et al., 2015). Recent emphases shifts in public health discussions stemming from debates around ‘Epistemologies of the South’ (De Sousa, 2011) propose that the route toward UHC in Mesoamerica is dependent on promoting “health sovereignty,” fostering a decolonial turn in favor of intercultural approaches that reflect the particular epidemiologies of the peoples (Basile, 2018). According to De Sousa (2010) and Laurell (2010) the neglected consideration of emic epistemologies in the shaping of public health policies should be contrasted with a turn toward an “ecology of knowledge-systems.” This perspective includes traditional medicine, particularly herbal medicine, which has been recognized as playing a key role toward providing culturally pertinent and accessible health coverage (Rocha-Buelvas, 2017) and is in line with the WHO’s guidelines, which pin-point acceptability as a factor fostering increased access to health provision services in diverse cultural settings (WHO, 2013).

Mesoamerica (from now on ‘MA’) is a term coined by Kirchoff (1943) and accepted by scholars to define a geographical region (Figure 1) inhabited by indigenous peoples that share several common cultural traits resulting from intense cultural interchange starting in the Early Preclassic period (Coe and Koontz, 2013). The advent of civilization in MA can be placed in the early second millennium BCE when the San Lorenzo Olmecs emerged in the region of today Veracruz (Mexico) and the Mokaya as the first socially stratified sedentary culture in the Soconusco region of Mexico and Guatemala on the Pacific coast (Clark, 1991, p. 13-26; Diehl, 2004, p. 129; Coe and Koontz, 2013). The common fundamental traits characterize the cultural area of MA and distinguish it from the rest of the Americas (Coe and Koontz, 2013, p. 9-10; Kirchhoff, 1943). Ranging from central Mexico to northern Central America, MA was home to several of the great civilizations of the Western Hemisphere, including the Olmecs, Maya, and Aztecs. Aztec medicine represented the culmination of a long cultural tradition uniting the different cultural groups of MA (Ortiz de Montellano, 1990). After the Conquest, the different health systems rapidly blended into a syncretic amalgamation combining indigenous and introduced elements (e.g., Ortiz de Montellano, 1975; Lozoya and Zolla, 1984; Ortiz de Montellano, 1990; Foster, 1994; Bye et al., 1995). Mirroring its outstanding cultural heritage, MA is also one of the world’s most biodiverse regions and among the most eminent centers of plant domestication (Vavilov, 1992; Smith, 1997; Myers et al., 2000; Ranere et al., 2009).

FIGURE 1
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Figure 1 Map of Mesoamerica (MA). The colored areas mark the geographic extent of the major linguistic groups: Mayan (green) in eastern MA and the Huasteca, Mixe-Zoque (blue) in the Isthmus of Tehuantepec region, Nahuatl (red) in central and western MA, Totonac (turquoise) in Veracruz, and Zapotec (yellow) in Oaxaca. The numbers 1–28 refer to the study codes in Table 1; the extents of the respective study sites are highlighted in white.

Epidemiology, Health Systems, and Integrative Medicine in MA

Mexico and Central America are undergoing a rapid health transition resulting in a “double burden of disease” as poverty related diseases coexist with modern lifestyle diseases (Frenk, 2006; Stevens et al., 2008; Puig et al., 2009; Gómez-Dantés et al., 2016).

As a result of a higher life expectancy, after the 1940s Mexico experienced a great demographic expansion going hand in hand with economic growth (Cabrera, 1994). Toward the end of the 1960s, however, concerns were raised about the economic sustainability of the soaring population (Cabrera, 1994) and in 1973 a new population policy was implemented (Alba and Potter, 1986). The Mexican Ministry of Health and Welfare (SSA) together with the Institute of Social Security (Instituto Mexicano del Seguro Social; IMSS) started to provide family planning counseling and contraceptive services free of charge through their national networks in 1973 (Alba and Potter, 1986). During the 1970s and until 1982 the political administrations expanded the Mexican health sector by increasing the number of hospitals, clinics and medical staff. This initiative included the establishment of over 3,000 rural health posts, 71 rural hospitals and trainee programs for community health workers including traditional midwifes. As a consequence, the family planning services reached communities and individuals that were not formally considered by the social security system (Alba and Potter, 1986). These measures resulted in a reduced population growth that was more accentuated in urban compared to rural areas and overall reduced poverty (Cabrera, 1994; Allen, 2007). In 1983 the IMSS started to monitor systematically the epidemiology in the marginalized rural communities. This data was used as a baseline for launching programs aimed at reducing morbidity and mortality culminating in a decrease of digestive infections, less malnutrition and better assistance during gestation, birth and postpartum period (Flores Alvarado and Morán Zenteno, 1989). In Guatemala in particular and Central America in general, emerging civil armed conflicts at the end of the 1960s, lasting into the 1990s, prevented health programs to comprehensively address the needs and reach out to the rural population, aggravating health disparities (Braveman et al., 2000; Flores et al., 2009).

Today, reduced burdens of infectious diseases are partially offset by the need for health care assistance caused by interpersonal violence and chronic illnesses (Stevens et al., 2008; PAHO, 2009; Acosta et al., 2011; Becerril-Montekio and López-Dávila, 2011; Bermúdez-Madriz et al., 2011; Gómez-Dantés et al., 2011a; Gómez-Dantés et al., 2011b; Gómez-Dantés et al., 2016). Despite promising effects of recent health system reforms, pronounced regional disparities in regard to health indicators within and between the countries of MA persist (Frenk, 2006; Stevens et al., 2008; Mokdad et al., 2015; Gómez-Dantés et al., 2016). Health inequities imply that infectious diseases – particularly diarrheal disorders and infections of the lower respiratory tract – and reproductive health still account for a considerable disease burden, particularly among marginalized, often indigenous, populations. Meanwhile, depressive and chronic diseases are becoming major health concerns (Frenk, 2006; Stevens et al., 2008; Mokdad et al., 2015; Gómez-Dantés et al., 2016). Especially type II diabetes mellitus and chronic kidney disease of unknown cause (CKDu), now also called epidemic of chronic kidney disease of nontraditional origin (CKDnt) pose increasing challenges to the health systems in the region (Barcelo et al., 2003; Barcelo et al., 2012; Kierans et al., 2013; Gómez-Dantés et al., 2016; Johnson et al., 2019; Wesseling et al., 2020). The endemic form of CKDu occurring in MA was previously called Mesoamerican nephropathy (MeN) and affects above all young male workers of the agricultural sector (Wesseling et al., 2013; Wijkström et al., 2013). The origin of CKDu (also MeN and CKDnt) seems to be primarily driven by occupational heat stress linked to dehydration (Wijkström et al., 2013; Wesseling et al., 2020).

With the partial exception of Belize, the national health systems throughout MA have a similar structure and suffer from considerable degrees of fragmentation and segmentation (Homedes and Ugalde, 2009; Puig et al., 2009; Acosta et al., 2011; Becerril-Montekio and López-Dávila, 2011; Bermúdez-Madriz et al., 2011; Gómez-Dantés et al., 2011a; Kierans et al., 2013; Mokdad et al., 2015). Typically, public sectors in MA countries are composed of the respective ministries of health, social security institutes, and up to seven additional service providers. While formal employees benefit from social security, the majority of the populations rely on the – at least theoretically – free healthcare provided by the ministries of health. Notwithstanding the constitutional guarantee of affordable healthcare to all, a considerable proportion of the population of each country has no de facto access to healthcare provision from the public sector; a deficit partially compensated for by a multitude of civil society organizations operating in the most marginalized areas, but perhaps more importantly, by traditional healers embedded in long-standing ethnomedical systems.

In Guatemala it is estimated that public investments cover only 40% of the costs for accessing healthcare services, and that most of these funds are centralized in urban and peri-urban areas (World Bank, 2016; Gomez et al., 2017). This exemplifies how marginalized communities in rural settings have to rely on a plurimedical system, where practitioners of traditional Maya medicine play a key role in providing affordable services (Ceron, 2010; Berger-González et al., 2016b; CMMM, 2016). Comprehension of this situation prompted the development of the Model for Inclusive Health in 2004 (Fort et al., 2011). This model implements the parallel coordination of patients between specialists in traditional medicine such as ajkum (~ herbalists), ajiyom (~ midwives), ajq’omaneel (~ physicians) and biomedical staff in the first and second levels of attention those working at community health posts and district health centers. The Inclusive Health Model required the implementation of new protocols of attention including ‘cultural syndromes’ such as susto (fright) ojeado (evil eye) or wuqub’ siwan (disease of the seven ravines; Taquira et al., 2016), and an understanding of associated botanical drug based therapies, so that the medical staff could be trained in coordinating safe patient care with Maya health specialists. For example, in the Cuilco health district alone, located in the western highlands of Guatemala, 360 traditional medicine practitioners coordinated interventions with 78 medical health staff (ISIS, 2019). The Inclusive Health Model was strongly promoted by the Ministry of Public Health between 2016 and 2017, which led to the inclusion of 40 plants into the “Norms for the Attention of the First and Second Levels” of the Ministry of Health (MSPAS, 2018, p. 835-863). In spite of this initial effort, the lack of evidence about the safety and efficacy of medicinal plants and associated botanical drugs employed by practitioners of traditional medicine are a limiting factor in the translation of these intercultural protocols.

Finally, a growing for-profit private sector offers care to the urban socio-economic elites. Each of these service providers has its own infrastructure and, despite recent efforts to harmonize service provision, the coordination between different health institutions is limited. Within the respective national health systems, the Ministry of Public Health plays the stewardship role, including the formulation of T&CM policies as well as integrating and regulating T&CM products and practitioners in the formal health systems (WHO, 2005; Homedes and Ugalde, 2009; Puig et al., 2009; Acosta et al., 2011; Becerril-Montekio and López-Dávila, 2011; Bermúdez-Madriz et al., 2011; Gómez-Dantés et al., 2011a; Kierans et al., 2013; Mokdad et al., 2015). Inefficiency in the public sector as well as the lack of cultural competency results in unsatisfactory perceived quality of care (Puig et al., 2009; Mokdad et al., 2015). In Mexico, the health-care delivery clinics in rural areas are run by the IMSS and the Mexican Ministry of Health and Welfare (SSA). Usually they are staffed with recent medical graduates who spend their obligatory year of postgraduate social service as well as with community health workers. This situation is, however, not the best basis for achieving quality, consistency, cultural sensitivity, and ultimately, patients’ confidence (Berlin and Berlin, 1996, p. 6) and is one of the reasons why traditional medicine has retained its important role in rural areas. For marginalized people, experiencing excessive financial, physical, or cultural barriers to care, traditional medicine often presents the only accessible healthcare option. Meanwhile herbal products provide popular treatment alternatives for urban socioeconomic elites and Latin American migrant communities (Lozoya and Zolla, 1984; Taddei-Bringas et al., 1999; Waldstein, 2006; Loera et al., 2007; WHO, 2013; Ladas et al., 2014; Alonso-Castro et al., 2017a). However, integrative efforts and official recognition of Mesoamerican Traditional Medicine are limited. Several countries lack national policies and programs on T&CM and Mexico is the only country in MA with a national pharmacopeia (WHO, 2005; Caceres Guido, 2015). Yet, from the 129 herbal drugs listed in the Mexican Herbal Pharmacopoeia only around 36 are native (FEUM, 2013). With respect to Guatemala, the National Vademecum on Medicinal Plants (Cáceres, 2009) containing validated information on 101 herbal drugs of which 42 are native, got the endorsement of the University of San Carlos and the Ministry of Public Health and was later adopted as a reference by the Central American Technical Regulation.

The emphasis on introduced taxa in formal phytotherapy in Latin America is due to an often lacking evidence base for native botanical drugs (Caceres Guido et al., 2015; Valdivia-Correa et al., 2016; Alonso-Castro et al., 2017b) and the relative good documentation of effectiveness and safety issues of herbal drugs present in the European and the US Pharmacopoeia (Lozoya and Zolla, 1984; Caceres Guido et al., 2015; Martins et al., 2019).

Medical concepts and health beliefs regarding disease etiology, diagnosis, and treatment show striking similarities throughout MA, notwithstanding the uniqueness of each cultural group’s ethnomedical system and individual case to case variations (Lozoya and Zolla, 1984; Weller et al., 2002; Groark, 2005; Kleinman and Benson, 2006; Balick et al., 2008; Berger-González et al., 2016a; Geck et al., 2017). Efforts to integrating traditional practitioners and practices into the formal health system have been met with limited success [but see Chary et al. (2018) and Hitziger et al. (2017)], partially due to a limited understanding of ethnomedical concepts and rural medicine as well as an a priori disesteem toward traditional medicine by formal health institutions and physicians (Lozoya and Zolla, 1984; Nigenda et al., 2001; Bye and Linares, 2015; Colon-Gonzalez et al., 2015). Formal health professionals in Mexico regularly prescribe and use herbal products yet lament the lack of T&CM-specific education and training material (Taddei-Bringas et al., 1999; Romero-Cerecero and Tortoriello-García, 2007; Alonso-Castro et al., 2017a). Meanwhile traditional healers rarely find successors and acculturation is changing patterns in transmission of traditional and local knowledge (Comerford, 1996; Balick et al., 2008; García-Hernández et al., 2015; Geck et al., 2016). Consequently, written sources of knowledge as well as popular media are increasingly shaping the medical systems of local and indigenous communities (Leonti, 2011; Geck et al., 2016).

Previous Cross-Cultural Comparisons and Compilations of Mesoamerican Herbal Medicine

Several national and regional compilations of medicinal plants exist in Mexico, covering over 3,000 botanical taxa (Argueta and Zolla, 1994; Bye et al., 1995). Unfortunately, these often demonstrate serious methodological deficits, particularly in regard to taxonomic identification and interpretation of ethnomedical data (Bye and Linares, 2015, p. 396-397). Further, the lacking quantification of traditional uses limit the utility of these compilations for the identification of cross-culturally salient taxa.

The first over-regional research program in the area aimed at the evaluation of the traditional use of botanical drugs in order to improve the quality of health care of marginalized populations was Tramil (Program of Applied Research to Popular Medicine in the Caribbean; Weniger, 1991; Boulogne et al., 2011). Tramil’s exclusive focus on the Caribbean implied that only very minor parts of MA were covered (Boulogne et al., 2011). Several studies compared the medicinal floras and ethnomedical concepts of closely related cultural groups within the same linguistic family (e.g., Berlin and Berlin, 1996; Leonti et al., 2003; Geck et al., 2016; Hitziger et al., 2016). Heinrich et al. (1998; 2014) conducted the most comprehensive cross-cultural analyses to date yet focused exclusively on gastrointestinal ailments. Additionally, several reviews exist on the treatment of emerging health concerns, specifically anxiety and depression, colorectal cancer, diabetes, and obesity (Alonso-Castro et al., 2015a; Cruz and Andrade-Cetto, 2015; Andrade-Cetto and Heinrich, 2016; Giovannini et al., 2016; Jacobo-Herrera et al., 2016; López-Rubalcava and Estrada-Camarena, 2016).

Objectives of This Analysis

T&CM contributes significantly to the health coverage of the population of MA, particularly in poor and underserved indigenous communities (WHO, 2013). Similarly, to the situation in MA, in most regions of the world, a wealth of information on T&CM has been recorded. Yet these data are often scattered, making it difficult for policy makers to regulate and integrate herbal products into primary health care. Despite over 400 million estimated regular users of T&CM in Latin America, systematic approaches to integrate T&CM in formal health systems are widely lacking (Caceres Guido et al., 2015). Given the shared cultural history, harmonizing regulations between different nations of MA is recommended (WHO, 2013, p. 41). A lack of pharmacological and toxicological data on even the most commonly used herbal drugs is often considered the principal limitation to integrative medicine in MA (Caceres Guido et al., 2015; Alonso-Castro et al., 2017a). National and international efforts have been conducted in Guatemala in order to establish integrative medicine at academic and public health levels and although official acceptance is limited, national interest and expectations are high (Cáceres, 2019). Further, there is a strong need to integrate T&CM into formal health education (Romero-Cerecero and Tortoriello-García, 2007; Alonso-Castro et al., 2017a). Hence, creating quantitative regional databases based on internationally published literature can be an effective means for advancing the integration of evidence-based T&CM and therefore contribute to achieving UHC.

In accordance with the strategic objectives outlined in the Traditional Medicine Strategy of the World Health Organization (WHO, 2013), we aim at establishing a consensus-driven knowledge base on herbal drugs used in Mesoamerican traditional medicine. The focus is on plants used as medicine by traditional healers in rural indigenous communities. The quantitative nature of the review will allow for the prioritization of taxa for pharmacological and clinical studies. The pharmacological evidence for the safety and efficacy of the cross-culturally most salient taxa is reviewed and important knowledge gaps are indicated. The review is intended as a baseline of evidence for regulators, health professionals, and consumers for making informed decisions on herbal drugs and phytomedicines. Hence, this review and the MAMPDB is seen as an essential first step for an improved integration of traditional medicine into the national health systems of Mexico and Central America.

Methods

The linguistic scope of this cross-cultural comparison is limited to the five groups that can be most closely linked to the cultural evolution of MA: Maya, Mixe-Zoque, Nahuatl, Totonac, and Zapotec (Kirchhoff, 1943; Campbell et al., 1986). Likewise, the geographic scope is limited to MA proper, excluding the frontier areas of northern Mexico and Central America, as these only temporally participated in MA (Coe and Houston, 2015: 13; Kirchhoff, 1943; Figure 1).

Published ethnobotanical and ethnopharmacological field studies related to the five linguistic groups were sought that met the minimum inclusion criteria of methodological transparency regarding data sampling, study location, population and taxonomic identification based on voucher specimens collected in situ. A comprehensive search on the online databases Medline (PubMed) and Scopus as well as the Swiss library network (swissbib) and the dissertations database ProQuest was conducted with the following search terms: ethnobotany OR ethnopharmacology OR “traditional medicine” OR “medicinal plants” OR “herbal medicine” AND Mesoamerica OR Mexico OR “Central America” Guatemala OR Belize OR “El Salvador” OR Honduras OR Maya OR Mixe OR Zoque OR Nahua OR Nahuatl OR Aztec OR Totonac OR Zapotec. Thus, 28 studies published between 1975 and 2016 were identified that met the geographic, linguistic, and methodological inclusion criteria to be considered by the MAMPDB (Table 1)1. Names and classification of linguistic groups follow glottolog 2.7 (Hammarström et al., 2016).

TABLE 1
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Table 1 Studies included in the Mesoamerican Medicinal Plant Database (MAMPDB).

All plant taxa with medicinal uses mentioned in the 28 studies were incorporated into the MAMPDB after verifying their taxonomic identity with www.theplantlist.org (accessed 06.06.2016). Family affiliations of angiosperms follow the more up-to-date APG IV (The Angiosperm Phylogeny Group, 2016). In case several members of the same genus are used interchangeably under the same vernacular name for the same purpose, the taxon is denoted Genus sp. Infraspecific taxa are not specified.

The medicinal uses were classified according to the second edition of the International Classification of Primary Care (ICPC; Table 2). The ICPC allows for classification of ethnomedical uses into 17 symptom-based categories, not requiring detailed diagnostics (WICC, 2004; Staub et al., 2015). The only modification made to the ICPC system refers to toothache, which was classified as a neurological rather than a digestive system disorder.

TABLE 2
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Table 2 Overview of the distribution of taxa and use-records of the Mesoamerican Medicinal Plant Database in the 17 International Classification of Primary Care (ICPC) categories.

For the species cited in at least nine studies (one third taken as an arbitrary threshold value) a comprehensive literature review of pharmacological data was conducted based on a literature search with the online databases Medline (PubMed), Scopus, and the Cochrane Library (Table 3). Preclinical and clinical data obtained with botanical drugs derived from the 98 medicinal plant species cited in at least nine studies are reported in correspondence to the predominant traditional uses (use-records). As an arbitrary threshold value predominant uses are defined here as those recorded in the same ICPC category by at least seven independent studies or alternatively, those most frequently recorded in an ICPC category in case no category was recorded in at least seven studies. A use-record is defined as a reported use per taxon and ICPC category in one study. Studies lacking methodological transparency or using doses unrealistically high from a therapeutic perspective were excluded from this review. We evaluated the available pharmacological and preclinical data in order to extrapolate on the safety and efficacy of clinical applications. We took the mode of application into account and considered the importance of cultural factors for the perceived effectiveness, which is to be distinguished from efficacy (Ortiz de Montellano, 1975; Last et al., 2001, p. 57-58; Moerman and Jonas, 2002; Witt, 2013). Therefore, we evaluated as potentially safe and effective also applications of herbal drugs for which no negative toxicological reports were available. Despite the human influence on the current distribution of plant taxa is not always exactly known we categorized the 98 species into natives and exotics, judging those species native which, due to their cultural importance, obtained a wide distribution range over South and MA prior to European conquest and colonization (e.g., Bixa orellana and Petiveria alliacea) as well as the pantropic species (e.g., Cissampelos pareira and Cocos nucifera).

TABLE 3
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Table 3 The cross-culturally most salient medicinal plant species in Mesoamerica (MA).

Results and Discussion

The Mesoamerican Medicinal Plant Database (MAMPDB)

The MAMPDB includes a total of 12,537 use-records for 2188 taxa (Table 2), including 1929 species and 259 taxa identified to the genus level only (Table 4.1 in the Supplementary Material), 995 genera (Table 4.2 in the Supplementary Material), and 185 families (Table 4.3 in the Supplementary Material). For more than half of the species (1,100; 57%) no cross-cultural consensus does exist and 36% of the genera are only recorded in one of the 28 studies incorporated into the database.

In the different ICPC categories herbal medicine and pharmaceuticals are not considered to the same extent appropriate solutions for the treatment of the various health problems. Therefore, the number of taxa and use-records associated with these categories do not directly reflect the epidemiological situation in rural MA but can provide some information. Several categories are poorly recognized in ethnomedical systems such as “B” (blood, blood forming organs and immune mechanism), “K” (Cardiovascular) and “T” (endocrine/metabolic and nutritional) while “Z” (social problems) is unlikely to be treated with medicine. Typically, the broad categories “digestive” (D) and “skin” (S) are among those with the highest number of associated medicinal plants and use-records (Table 2). Musculoskeletal ailments (L) are often treated with massages by traditional healers called ‘sobadores’ or ‘ajpamaj’ (Ankli et al., 1999; Leonti et al., 2001; Berger-González et al., 2016b; Geck et al., 2016) while midwifes give massages for problems of the lower female organs (X) (Weimann and Heinrich, 1997; Ankli et al., 1999; Michel et al., 2016). Measures for family planning (W) are provided by the IMSS in collaboration with MEXFAM. For treating and preventing several ailments of the urological system (U) it is important to drink copiously and flush the urinary tract. This means that ailments and interventions with respect to the categories B, L, K, T, U, W, X, and Z are probably more frequent than suggested by the number of use-records related to botanical drugs.

The many species of Asteraceae (226), Fabaceae (194), Euphorbiaceae (85) and Lamiaceae (79) reported for medicinal purposes in the 28 studies (Table 4.3 in the Supplementary Material) reflect the floristic representation of these plant families in the region (see Bye and Linares, 2015, p. 394). The use consensus of Asteraceae is on digestive (D; 54% spp./19.5% use-records) and inflammatory skin disorders (S; 47.8% spp./12.8% use-records) but the characteristic presence of cytotoxic sesquiterpene lactones in this family can lead to allergenic reactions (Siedle et al., 2004). The family with the highest share of species for skin disorders in the MAMPDB are the Solanaceae (66.2% spp./20.8% use-records) and the Euphorbiaceae (64.7% spp./24.7% use-records.), the latter notorious for their proinflammatory properties (Evans and Taylor, 1983). The family showing the highest share for A ‘unspecified’ are the Solanaceae (61.8% spp./18.6% use-records), Lamiaceae are most frequently used for digestive problems (D; 73.4% spp./20% use-records) and Fabaceae for skin disorders (S; 51% spp./15.6% use-records).

Consensus Analysis

The consensus of those 98 species, for which a therapeutic use has been documented in at least nine (one third taken as an arbitrary threshold value) of the 28 independent studies is presented in Table 3 together with a critical evaluation of the pharmacological and toxicological evidence based on existing literature. It highlights the most frequently cited taxa in the MAMPDB, which have roots in Olmec, Maya, Zapotec and Aztec as well as traditional Mediterranean medicine. Most of the 98 herbal drug species are either grown in home-gardens or thrive in the vegetation surrounding the villages and are thus easily available. Several are also sold on local markets for food purposes, including spices, herbs, vegetables and fruits. Of the 98 species 68 are native to MA (Table 3). Of those 22 considered effective and safe for skin problems (S) 17 are native to MA while of the 13 considered effective and safe for respiratory ailments (R) only 3 are native. For digestive (D), skin (S) and respiratory (R) problems as well as for the category ‘general and unspecified’ (A) among the 98 species a range of effective and safe herbal drug-based treatment options exist (Table 3).

Typically, many of the herbal drugs used against diarrhea (D) are rich in tannins and polyphenols (Heinrich, 1998), such as the bark of Byrsonima crassifolia, Guazuma ulmifolia, and Mangifera indica, leaves of Psidium guajava and Mangifera indica, unripe fruits of Musa × paradisiaca and fruit skin of Punica granatum. Those used altogether for gastrointestinal plain, cramps and diarrhea such as the leaves of Eryngium foetidum and Litsea glaucescens, the herb of Artemisia absinthium, the root of Cissampelos pareira and the zest of Citrus aurantiifolia are aromatic and/or bitter tasting drugs. Those herbal drugs effective and safe used for category ‘A’ fall under the sub-category of ‘general pain’, ‘weakness’ and ‘feeling ill’ (ICPC) and include those herbal species also used in ritual healing. These are often aromatic, essential oil-bearing plants such as Ocimum basilicum, O. campechianum, Tagetes lucida or Piper amalago. The ritual cleansing ceremony called “limpia” using aromatic herbs and lotions to brush away bad spirits from the patient is a typical therapeutic practice in MA (Zamora-Martínez and Pascual Pola, 1992). The leaves of Ocimum spp. are used either as an infusion or applied topically against headache (N) while the flowers and zest of Citrus sinensis and C. aurantium serve as infusions to treat anxiety and stress (P). The practice of using essential oil rich herbal drugs for treating the ICPC categories A, P and N remind of aromatherapy, which has been found effective in clinical trials focusing on stress and anxiety related disorders (Perry and Perry, 2006; Linck et al., 2010). There seems to be a lack of safe and effective diuretics as well as disinfectants of the urinary tract (only corn silk and fruits of Sechium edule (chayote) among Table 3). For muscular problems (L) nowadays often massages with commercialized balms are used and assistance during pregnancy, childbearing and family planning (W) is provided in Mexico by the IMSS in collaboration with trained local midwifes.

For several important medicinal species there is very limited evidence for either safety or efficacy or altogether, including but not limited to Tagetes erecta, Piper auritum, Byrsonima crassifolia, Bursera simaruba, Artemisia ludoviciana, Hyptis verticillata, Spondias purpurea Tradescantia zebrina Crescentia cujete, Parmentiera aculeata, Piper amalago, Baccharis inamoena, Bougainvillea glabra, Lepidium virginicum, Malvaviscus arboreus, Mimosa albida, Solanum lycopersicum, Cornutia pyramidata, Dorstenia contrajerva, Tagetes filifolia and Jatropha curcas (Table 3). This situation emphasizes the lacking knowledge base and the concerns regarding toxicity of native botanical drug species widely used in traditional medicine throughout MA (Caceres Guido et al., 2015; Valdivia-Correa et al., 2016; Alonso-Castro et al., 2017b).

According to the WHO guidelines for the assessment of herbal medicines (WHO, 1996, p. 181) a principle for the safety assessment of herbal medicines should be the traditional use of the product “without demonstrated harm” while “no specific restrictive regulatory action should be undertaken unless new evidence demands a revised risk-benefit assessment.” Yet even though a track record of traditional medical use can provide some evidence about the safety of herbal drugs and their applications it is necessary to point out that ‘natural’ is not to be confounded with safe, a common misconception among consumers of herbal drugs (WHO, 2013).

A well-studied case of toxic plant materials are aristolochic acids containing botanical drugs deriving from the Aristolochiaceae (Arlt et al., 2002; Michl et al., 2014). Aristolochic acids are nephrotoxic and carcinogenic and potentially contained in botanical drugs obtained from 14 different Aristolochia species present in the MAMPDB. The drugs obtained from Aristolochia spp. are often used for digestive problems and totaled 95 use-records in the MAMPDB (Table 4.1 in the Supplementary Material). The time lag between the onset of chronic intoxication and the manifestation of eventually lethal kidney disorders is the reason why the resulting pathology is difficult for the general population to associate with the consumption of Aristolochia spp. Clearly safety concerns prevail above all with systemic applications. Also the use of castor oil plant seeds as an emetic and purgative is risky (Aplin and Eliseo, 1997) and due to the high content of the hepatotoxic and carcinogenic safrole the leaves of Piper auritum, which are also widely used as a condiment for pork tamales (wrapped maize dough cakes), should be used in low doses when applied orally. Anthranoid rich material (bitterness as a proxy) of Aloe vera is regarded as unsafe upon prolonged oral applications and particularly during pregnancy as the resulting increased blood flow to the uterus can induce abortion (Schulz et al., 2012, p. 250). The leaves of Bryophyllum pinnatum contain cardiotoxic bufadienolids, the aromatic leaves of Lantana camara hepatotoxic metabolites, the leaves of Phyla scaberrima high amounts of neurotoxic camphor, and the aerial parts of Parthenium hysterophorus toxic sesquiterpenelactones and are thus all unsafe depending on the dose ingested. Also applying the latex of Argemone mexicana to the eyes, the latex of Asclepias curassavica to aching teeth and using Ruta chalepensis during pregnancy are to be regarded unsafe.

The guidelines for the “Appropriate Use of Herbal Medicines” (WHO, 1998, p. 2) state that “it is necessary to make a systematic inventory and assessment (preclinical and clinical) of medicinal plants; to introduce measures on the regulation of herbal medicines to ensure quality control of herbal products by using modern techniques, applying suitable standards and good manufacturing practices; and to include herbal medicines in the national standard or pharmacopoeia.” A relatively cost-effective way for conducting clinical trials are retrospective treatment-outcome studies (RTO studies), which use questionnaires for the collection of information from a representative sample of the population (Graz et al., 2005; Graz et al., 2007). RTO studies assess retrospectively the effectiveness of herbal preparation and treatments for defined medical syndromes and clinical manifestations (Graz et al., 2005; Willcox et al., 2011). While the case of Aristolochia spp. derived products showcases that herbal drugs are not always safe, those with a traditional clinical track record and above all food items, usually considered safe, qualify for RTO studies (WHO, 1998; Willcox et al., 2011).

The quantitative approach and assessment of the 98 most frequently used medicinal taxa included in the MAMPDB highlights those herbal drugs with the highest intercultural acceptance as well as those applications potentially unsafe. The higher probability of exotic herbal drugs to be considered safe and efficacious (Table 2) is related to the better overall research situation of herbal drugs used in the European and the US Pharmacopoeia (Martins et al., 2019). However, Table 3 includes several native herbal drugs uses as food such as spices and culinary herbs and constitutes potential starting points for RTO studies. While the intercultural consensus can give some indications about the safety and perceived effectiveness, intriguingly Graz et al. (2005) found that the treatment of malaria in Mali showed no significant correlation between cultural consensus and the best patient progress, underlining the strength of RTOs being complementary to ethnopharmacological field studies.

The list of medicinal species reviewed in Table 3 constitutes a data collection that can be drawn on by the Mexican Herbal Pharmacopoeia Committee for increasing the Appendix VI (list of species with medical use in Mexico). Appendix VI is the prelude to the monographs of medicinal plants contained in the Pharmacopoeia and could be used to promote a better integration of native Mesoamerican species into that regulatory document. It should also be considered that knowledge about herbal remedies is increasingly shaped by literature and popular media, through which global trends in T&CM are introduced to local communities.

Conclusions

Through the evaluation of the MAMPDB we have highlighted a group of locally available medicinal plants, yielding products with a high inter-cultural consensus of use and track record of traditional use. However, the results from preclinical in vitro or in vivo studies are only a proxy for medical efficacy in humans. Especially for native herbal drugs data about safety and effectiveness is limited. Commonly used cross-culturally salient botanical drugs, which are considered safe but for which data on effectiveness is lacking are ideal candidates for treatment outcome studies. These could be conducted at local health clinics and in collaboration with the respective ministries of health and social security institutes. Retrospective treatment outcome studies constitute a valid tool for a culturally sensitive evaluation of traditional medicines including the psychosocial dimension of healing. Collaborations between the medical staff of local health clinics with local health workers and practitioners of traditional medicine have the potential to close cultural gaps and medical misconceptions that preclude the implementation of intercultural models of healthcare attention. It would facilitate an enhanced acceptance and integration of different medical thoughts and foster communication between traditional health practitioners, patients and health professionals trained in Western biomedicine. A closer collaboration between practitioners of biomedical and traditional medical systems has the potential to increase affordability, accessibility and cultural acceptability of health care.

Similarly, to the situation in MA, in most regions of the world, a wealth of information on traditional and complementary medicine (T&CM) has been recorded. Yet these data are often scattered, making it difficult for policy makers to regulate and integrate traditionally used botanical products while existing compendia are often outdated. Creating quantitative regional databases that are based on internationally published literature can serve as effective means in the advancement of the integration of evidence-based T&CM and contribute to achieving UHC. It also constitutes a tool for responding to changing epidemiological landscapes and consumer preferences.

Author Contributions

MG and ML designed the review. MG, MB-G, LC, SC, MH, and ML wrote the paper.

Funding

This project has received funding from the European Union’s Seventh Framework Program for research, technological development and demonstration under grant agreement no. 606895.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2020.01160/full#supplementary-material

Footnotes

  1. ^ Four studies (no. 15, 16, 20, 24) focus on a specific disease category, whereas medicinal uses are not detailed in study no. 17, due to concerns about intellectual property rights.

References

Abarca-Vargas, R., Petricevich, V. L. (2018). Bougainvillea genus: A review on phytochemistry, pharmacology, and toxicology. Evid. Based Complement. Alternat. Med., 9070927. doi: 10.1155/2018/9070927

PubMed Abstract | CrossRef Full Text | Google Scholar

Abdelhafez, O. H., Fawzy, M. A., Fahim, J. R., Desoukey, S. Y., Krischke, M., Mueller, M. J., et al. (2018). Hepatoprotective potential of Malvaviscus arboreus against carbon tetrachloride-induced liver injury in rats. PloS One 13, e0202362. doi: 10.1371/journal.pone.0202362

PubMed Abstract | CrossRef Full Text | Google Scholar

Abdulaziz, A. A., Dapar, M. L. G., Manting, M. M. E., Torres, M. A. J., Aranas, A. T., Mindo, R. A. R., et al. (2019). Qualitative evaluation of the antimicrobial, antioxidant, and medicinally important phytochemical constituents of the ethanolic extracts of the leaves of Gliricidia sepium (Jacq.) Walp. Pharmacophore 10, 72–83.

Google Scholar

Accioly, M. P., Bevilaqua, C. M. L., Rondon, F. C. M., de Morais, S. M., Machado, L. K. A., Almeida, C. A., et al. (2012). Leishmanicidal activity in vitro of Musa paradisiaca L. and Spondias mombin L. fractions. Vet. Parasitol. 187, 79–84. doi: 10.1016/j.vetpar.2011.12.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Acosta, M., Sáenz, M., del, R., Gutiérrez, B., Bermúdez, J. L. (2011). Sistema de salud de El Salvador. Salud Publica Mex. 53, s188–s196.

PubMed Abstract | Google Scholar

Adedapo, A., Babarinsa, O., Oyagbemi, A., Adedapo, A., Omobowale, T. (2016). Cardiotoxicity study of the aqueous extract of corn silk in rats. Mac. Vet. Rev. 39, 43–49. doi: 10.1515/macvetrev-2015-0065

CrossRef Full Text | Google Scholar

Adeleye, I. A., Opiah, L. (2003). Antimicrobial activity of extracts of local cough mixtrues on upper respiratory tract bacterial pathogens. West Indian Med. J. 52, 188–190.

PubMed Abstract | Google Scholar

Affonso, R. C., Voytena, A. P., Fanan, S., Pitz, H. D., Coelho, D. S., Horstmann, A. L., et al. (2016). Phytochemical composition, antioxidant activity, and the effect of the aqueous extract of coffee (Coffea arabica L.) bean residual press cake on the skin wound healing. Oxid. Med. Cell. Longev. 2016, 1923754. doi: 10.1155/2016/1923754

PubMed Abstract | CrossRef Full Text | Google Scholar

Aguilar, L. C., Macías, S., Chagoya, A., Cárdenas, A., Díaz, P., Cantú, J. M. (1993). Antidiabetic activity of Tecoma stans in rats. Fitoterapia 64, 304–305.

Google Scholar

Aguilar, H. H. G., De Gives, P. M., Sánchez, D. O. S., Arellano, M. E. L., Hernández, E. L., Aroche, U. L., et al. (2008). In vitro nematocidal activity of plant extracts of Mexican flora against Haemonchus contortus fourth larval stage. Ann. N. Y. Acad. Sci. 1149, 158–160. doi: 10.1196/annals.1428.075

PubMed Abstract | CrossRef Full Text | Google Scholar

Aguilar-Santamaría, L., Tortoriello, J. (1996). Anticonvulsant and sedative effects of crude extracts of Ternstroemia pringlei and Ruta chalepensis. Phytother. Res. 10, 531–533. doi: 10.1002/(SICI)1099-1573(199609)10:6<531::AID-PTR888>3.0.CO;2-Z

CrossRef Full Text | Google Scholar

Aguilar-Santamaría, L., Ramírez, G., Nicasio, P., Alegría-Reyes, C., Herrera-Arellano, A. (2009). Antidiabetic activities of Tecoma stans (L.) Juss. ex Kunth. J. Ethnopharmacol. 124, 284–288. doi: 10.1016/j.jep.2009.04.033

PubMed Abstract | CrossRef Full Text | Google Scholar

Aguiñiga-Sánchez, I., Cadena-Iñiguez, J., Santiago-Osorio, E., Gómez-García, G., Mendoza-Núñez, V. M., Rosado-Pérez, J., et al. (2017). Chemical analyses and in vitro and in vivo toxicity of fruit methanol extract of Sechium edule var. nigrum spinosum. Pharm. Biol. 55, 1638–1645. doi: 10.1080/13880209.2017.1316746

PubMed Abstract | CrossRef Full Text | Google Scholar

Akaberi, M., Sobhani, Z., Javadi, B., Sahebkar, A., Emami, S. A. (2016). Therapeutic effects of Aloe spp. in traditional and modern medicine: A review. Biomed. Pharmacother. 84, 759–772. doi: 10.1016/j.biopha.2016.09.096

PubMed Abstract | CrossRef Full Text | Google Scholar

Akele, B. (2013). In vivo antimalarial activity of areal part extracts of Gardenia lutea and Sida rhombifolia. Int. J. Res. Pharmacol. Pharmacother. 2, 234–241.

Google Scholar

Akinpelu, D. A., Obuotor, E. M. (2000). Antibacterial activity of Nicotiana tabacum leaves. Fitoterapia 71, 199–200. doi: 10.1016/S0367-326X(99)00148-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Akinpelu, D. A., Aiyegoro, O. A., Akinpelu, O. F., Okoh, A. I. (2015). Stem bark extract and fraction of Persea americana (Mill.) exhibits bactericidal activities against strains of Bacillus cereus associated with food poisoning. Molecules 20, 416–429. doi: 10.3390/molecules20010416

CrossRef Full Text | Google Scholar

Alanís, A. D., Calzada, F., Cervantes, J. A., Torres, J., Ceballos, G. M. (2005). Antibacterial properties of some plants used in Mexican traditional medicine for the treatment of gastrointestinal disorders. J. Ethnopharmacol. 100, 153–157. doi: 10.1016/j.jep.2005.02.022

PubMed Abstract | CrossRef Full Text | Google Scholar

Alba, F., Potter, J. E. (1986). Population and Development in Mexico since 1940: An Interpretation. Popul. Dev. Rev. 12, 47–75. doi: 10.2307/1973351

CrossRef Full Text | Google Scholar

Alcorn, J. B. (1984). Huastec Mayan Ethnobotany (Austin: University of Texas Press).

Google Scholar

Alerico, G. C., Beckenkamp, A., Vignoli-Silva, M., Buffon, A., von Poser, G. L. (2015). Proliferative effect of plants used for wound healing in Rio Grande do Sul state, Brazil. J. Ethnopharmacol. 176, 305–310. doi: 10.1016/j.jep.2015.11.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Al-Harbi, R., Shaaban, M., Al-Wegaisi, R., Moharram, F., El-Rahman, O. A., El-Messery, S. (2018). Antimicrobial activity and molecular docking of tannins from Pimenta dioica. Lett. Drug Des. Discovery 15, 508–515. doi: 10.2174/1570180814666170810113850

CrossRef Full Text | Google Scholar

Allen, R. H. (2007). The role of family planning in poverty reduction. Obstet. Gynecol. 110, 999–1002. doi: 10.1097/01.AOG.0000287063.32004.23

PubMed Abstract | CrossRef Full Text | Google Scholar

Alonso-Castro, A. J., Miranda-Torres, A. C., González-Chávez, M. M., Salazar-Olivo, L. A. (2008). Cecropia obtusifolia Bertol and its active compound, chlorogenic acid, stimulate 2-NBDglucose uptake in both insulin-sensitive and insulin-resistant 3T3 adipocytes. J. Ethnopharmacol. 120, 458–464. doi: 10.1016/j.jep.2008.09.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Alonso-Castro, A. J., Maldonado-Miranda, J. J., Zarate-Martinez, A., del Rosario Jacobo-Salcedo, M., Fernández-Galicia, C., Figueroa-Zuñiga, L. A., et al. (2012a). Medicinal plants used in the Huasteca Potosina, México. J. Ethnopharmacol. 143, 292–298. doi: 10.1016/j.jep.2012.06.035

PubMed Abstract | CrossRef Full Text | Google Scholar

Alonso-Castro, A. J., Ortiz-Sánchez, E., Domínguez, F., Arana-Argáez, V., Juárez-Vázquez, M., del, C., et al. (2012b). Antitumor and immunomodulatory effects of Justicia spicigera Schltdl (Acanthaceae). J. Ethnopharmacol. 141, 888–894. doi: 10.1016/j.jep.2012.03.036

PubMed Abstract | CrossRef Full Text | Google Scholar

Alonso-Castro, A. J., Domínguez, F., Zapata-Morales, J. R., Carranza-Álvarez, C. (2015a). Plants used in the traditional medicine of Mesoamerica (Mexico and Central America) and the Caribbean for the treatment of obesity. J. Ethnopharmacol. 175, 335–345. doi: 10.1016/j.jep.2015.09.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Alonso-Castro, A. J., Balleza-Ramos, S., Hernández-Morales, A., Zapata-Morales, J. R., González-Chávez, M. M., Carranza-Álvarez, C. (2015b). Toxicity and antinociceptive effects of Hamelia patens. Rev. Bras. Farmacogn. 25, 170–176. doi: 10.1016/j.bjp.2015.03.007

CrossRef Full Text | Google Scholar

Alonso-Castro, A. J., Domínguez, F., Maldonado-Miranda, J. J., Castillo-Pérez, L. J., Carranza-Álvarez, C., Solano, E., et al. (2017a). Use of medicinal plants by health professionals in Mexico. J. Ethnopharmacol. 198, 81–86. doi: 10.1016/j.jep.2016.12.038

PubMed Abstract | CrossRef Full Text | Google Scholar

Alonso-Castro, A. J., Domínguez, F., Ruiz-Padilla, A. J., Campos-Xolalpa, N., Zapata-Morales, J. R., Carranza-Alvarez, C., et al. (2017b). Medicinal plants from North and Central America and the Caribbean considered toxic for humans: the other side of the coin. Evid. Based Complement. Alternat. Med. 2017:9439868. doi: 10.1155/2017/9439868

PubMed Abstract | CrossRef Full Text | Google Scholar

Alotaibi, S. M., Saleem, M. S., Al-humaidi, J. G. (2018). Phytochemical contents and biological evaluation of Ruta chalepennsis L. growing in Saudi Arabia. Saudi Pharm. J. 26, 504–508. doi: 10.1016/j.jsps.2018.02.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Al-Said, M. S., Tariq, M., Al-Yahya, M. A., Rafatullah, S., Ginnawi, O. T., Ageel, A. M. (1990). Studies on Ruta chalepensis, an ancient medicinal herb still used in traditional medicine. J. Ethnopharmacol. 28, 305–312. doi: 10.1016/0378-8741(90)90081-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Álvarez-Acosta, T., León, C., Acosta-González, S., Parra-Soto, H., Isabel Cluet-Rodriguez, I., Rosario Rossell, M. R., et al. (2009). Beneficial role of green plantain [Musa paradisiaca] in the management of persistent diarrhea: A prospective randomized trial. J. Am. Coll. Nutr. 28, 169–176. doi: 10.1080/07315724.2009.10719768

PubMed Abstract | CrossRef Full Text | Google Scholar

Alzoreky, N. S., Nakahara, K. (2003). Antibacterial activity of extracts from some edible plants commonly consumed in Asia. Int. J. Food Microbiol. 80, 223–230. doi: 10.1016/S0168-1605(02)00169-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Amid, A., Semail, S., Jamal, P. (2011). Tomato leaves methanol extract possesses anti-inflammatory activity via inhibition of lipopolysacharide (LPS)-induced prostaglandin (PGE2). Afr. J. Biotechnol. 10, 18674–18678. doi: 10.5897/AJB11.2737

CrossRef Full Text | Google Scholar

Amutha, K., Selvakumari, U. (2016). Wound healing activity of methanolic stem extract of Musa paradisiaca Linn. (Banana) in Wistar albino rats. Int. Wound J. 13, 763–767. doi: 10.1111/iwj.12371

PubMed Abstract | CrossRef Full Text | Google Scholar

Anaya-Eugenio, G. D., Rivero-Cruz, I., Bye, R., Linares, E., Mata, R. (2016). Antinociceptive activity of the essential oil from Artemisia ludoviciana. J. Ethnopharmacol. 179, 403–411. doi: 10.1016/j.jep.2016.01.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Andersen, A. (2007). Cosmetic Ingredient Review: Final report on the safety assessment of Aloe andongensis Extract, Aloe andongensis Leaf Juice, Aloe arborescens Leaf Extract, Aloe arborescens Leaf Juice, Aloe arborescens Leaf Protoplasts, Aloe barbadensis Flower Extract, Aloe barbadensis Leaf, Aloe barbadensis Leaf Extract, Aloe barbadensis Leaf Juice, Aloe barbadensis Leaf Polysaccharides, Aloe barbadensis Leaf Water, Aloe ferox Leaf Extract, Aloe ferox Leaf Juice, and Aloe ferox Leaf Juice Extract. Int. J. Toxicol. 26, 1–50.

Google Scholar

Andrade-Cetto, A., Heinrich, M. (2005). Mexican plants with hypoglycaemic effect used in the treatment of diabetes. J. Ethnopharmacol. 99, 325–348. doi: 10.1016/j.jep.2005.04.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Andrade-Cetto, A., Heinrich, M. (2016). Introduction to the Special Issue: The Centre of the Americas – An ethnopharmacology perspective. J. Ethnopharmacol. 187, 239–240. doi: 10.1016/j.jep.2016.04.026

PubMed Abstract | CrossRef Full Text | Google Scholar

Andrade-Cetto, A. (2009). Ethnobotanical study of the medicinal plants from Tlanchinol, Hidalgo, México. J. Ethnopharmacol. 122, 163–171. doi: 10.1016/j.jep.2008.12.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Ankli, A., Sticher, O., Heinrich, M. (1999). Medical ethnobotany of the Yucatec Maya: healers’ consensus as a quantitative criterion. Econ. Bot. 53, 144–160. doi: 10.1007/BF02866493

CrossRef Full Text | Google Scholar

Ankli, A. S. (2000). Yucatec Mayan medicinal plants: ethnobotany, biological evaluation and phytochemical study of Crossopetalum gaumeri (Zurich: PhD dissertation at the Swiss Federal Institute of Technology).

Google Scholar

Anonymous (2007). Final report on the safety assessment of Ricinus communis (castor) seed oil, hydrogenated castor oil, glyceryl ricinoleate, glyceryl ricinoleate SE, ricinoleic acid, potassium ricinoleate, sodium ricinoleate, zinc ricinoleate, cetyl ricinoleate, ethyl ricinoleate, glycol ricinoleate, isopropyl ricinoleate, methyl ricinoleate, and octyldodecyl ricinoleate. Int. J. Toxicol. 26, 31–77. doi: 10.1080/10915810701663150

PubMed Abstract | CrossRef Full Text | Google Scholar

Aplin, P. J., Eliseo, T. (1997). Ingestion of castor oil plant seeds. Med. J. Aust. 167, 260–261. doi: 10.5694/j.1326-5377.1997.tb125050.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Arbo, M. D., Larentis, E. R., Linck, V. M., Aboy, A. L., Pimentel, A. L., Henriques, A. T., et al. (2008). Concentrations of p-synephrine in fruits and leaves of Citrus species (Rutaceae) and the acute toxicity testing of Citrus aurantium extract and p-synephrine. Food Chem. Toxicol. 46, 2770–2775. doi: 10.1016/j.fct.2008.04.037

PubMed Abstract | CrossRef Full Text | Google Scholar

Argueta, A., Zolla, C. (1994). Nueva bibliografía de la medicina tradicional mexicana (Mexico City: Instituto Nacional Indigenista).

Google Scholar

Arlt, V. M., Stiborova, M., Schmeiser, H. H. (2002). Aristolochic acid as a probable human cancer hazard in herbal remedies: a review. Mutagenesis 17, 265–277. doi: 10.1093/mutage/17.4.265

PubMed Abstract | CrossRef Full Text | Google Scholar

Arnason, T., Uck, F., Lambert, J., Hebda, R. (1980). Maya medicinal plants of San Jose Succotz, Belize. J. Ethnopharmacol. 2, 345–364. doi: 10.1016/S0378-8741(80)81016-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Arroyo, A. R., Chacón, B., Maki, K. (2004). Screening and selection of plants by positive pharmacologic effect on jejunum muscular contractility. Pharm. Biol. 42, 24–29. doi: 10.1080/13880200490505357

CrossRef Full Text | Google Scholar

Atta, A. H., Alkofahi, A. (1998). Anti-nociceptive and anti-inflammatory effects of some Jordanian medicinal plant extracts. J. Ethnopharmacol. 60, 117–124. doi: 10.1016/S0378-8741(97)00137-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Augustine, B. B., Dash, S., Lahkar, M., Lihite, R. J., Samudrala, P. K., Pitta, S. (2013). Effect of Mirabilis jalapa Linn. flowers in experimentally induced arthritis and consecutive oxidative stress. Int. J. Pharm. Pharm. Sci. 5, 190–193.

Google Scholar

Aviello, G., Abenavoli, L., Borrelli, F., Capasso, R., Izzo, A. A., Lembo, F., et al. (2009). Garlic: empiricism or science? Nat. Prod. Commun. 4, 1785–1796. doi: 10.1177/1934578X0900401231

PubMed Abstract | CrossRef Full Text | Google Scholar

Ayaz, E., Turel, I., Gul, A., Yilmaz, O. (2008). Evaluation of the anthelmentic activity of garlic (Allium sativum) in mice naturally infected with Aspiculuris tetraptera. Recent Pat. Antiinfect. Drug Discovery 3, 149–152. doi: 10.2174/157489108784746605

CrossRef Full Text | Google Scholar

Ayissi Mbomo, R., Gartside, S., Ngo Bum, E., Njikam, N., Okello, E., McQuade, R. (2011). Effect of Mimosa pudica (Linn.) extract on anxiety behaviour and GABAergic regulation of 5-HT neuronal activity in the mouse. J. Psychopharmacol. 26, 575–583. doi: 10.1177/0269881111398686

PubMed Abstract | CrossRef Full Text | Google Scholar

Badgujar, S. B., Patel, V. V., Bandivdekar, A. H. (2014). Foeniculum vulgare Mill: A Review of Its Botany, Phytochemistry, Pharmacology, Contemporary Application, and Toxicology. Biomed. Res. Int., 842674. doi: 10.1155/2014/842674

PubMed Abstract | CrossRef Full Text | Google Scholar

Bakht, J., Azra, Shafi, M. (2012). Antimicrobial activity of Nicotiana tabacum using different solvents extracts. Pakistan J. Bot. 44, 459–463.

Google Scholar

Balick, M. J., De Gezelle, J. M., Arvigo, R. (2008). Feeling the pulse in Maya medicine: An endangered traditional tool for diagnosis, therapy, and tracking patients’ progress. Explor. J. Sci. Heal. 4, 113–119. doi: 10.1016/j.explore.2007.12.002

CrossRef Full Text | Google Scholar

Ban, J. O., Oh, J. H., Kim, T. M., Kim, D. J., Jeong, H.-S., Han, S. B., et al. (2009). Anti-inflammatory and arthritic effects of thiacremonone, a novel sulfurcompound isolated from garlic via inhibition of NF-κB. Arthritis Res. Ther. 11, R145–R145. doi: 10.1186/ar2819

PubMed Abstract | CrossRef Full Text | Google Scholar

Barbosa-Ferreira, M., Dagli, M. L., Maiorka, P. C., Górniak, S. L. (2005). Sub-acute intoxication by Senna occidentalis seeds in rats. Food Chem. Toxicol. 43, 497–503. doi: 10.1016/j.fct.2004.11.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Barcelo, A., Aedo, C., Rajpathak, S., Robles, S. (2003). The cost of diabetes in Latin America and the Caribe. B. World Health Organ. 81, 19–27.

Google Scholar

Barcelo, A., Gregg, E. W., Gerzoff, R. B., Wong, R., Perez Flores, E., Ramirez-Zea, M., et al. (2012). Prevalence of diabetes and intermediate hyperglycemia among adults from the first multinational study of noncommunicable diseases in six Central American countries. Diabetes Care 35, 738–740. doi: 10.2337/dc11-1614

PubMed Abstract | CrossRef Full Text | Google Scholar

Bashir, S., Gilani, A. H. (2008). Studies on the antioxidant and analgesic activities of Aztec marigold (Tagetes erecta) flowers. Phyther. Res. 22, 1692–1694. doi: 10.1002/ptr.2550

CrossRef Full Text | Google Scholar

Basille, G. (2018). La Salud Internacional Sur Sur: Hacia un giro decolonial z epistemológico. II Dossiers Salud Internacional Sur Sur, CLACSO (República Dominicana: FLACSO).

Google Scholar

Becerril-Montekio, V., López-Dávila, L. (2011). Sistema de salud de Guatemala. Salud Pública Mex. 53, s197–s208.

PubMed Abstract | Google Scholar

Benskin, L. L. L. (2013). A review of the literature informing affordable, available wound management choices for rural areas of tropical developing countries. Ostomy/wound Manage. 59, 20–41. doi: 10.25270/owm.2013.10.2041

CrossRef Full Text | Google Scholar

Berger-González, M., Gharzouzi, E., Renner, C. (2016a). Maya healers’ conception of cancer as compared to Western medicine. J. Glob. Oncol. 2, 56–67. doi: 10.1200/JGO.2015.00108

PubMed Abstract | CrossRef Full Text | Google Scholar

Berger-González, M., Vides, A., Heinrich, M., Strauss, S., Taquira, S., Krütli, P. (2016b). Relationships that heal: Going beyond the patient-healer dyad in Mayan therapy. Med. Antropol. 35, 353–367. doi: 10.1080/01459740.2016.1141408

CrossRef Full Text | Google Scholar

Berlin, E. A., Berlin, B. (1996). Medical ethnobotany of the Highland Maya of Chiapas, Mexico: the gastrointestinal diseases (Princeton: Princeton University Press).

Google Scholar

Bermúdez-Madriz, J. L., Sáenz, M. R., Muiser, J., Acosta, M. (2011). Sistema de salud de Honduras. Salud Publica Mex. 53, s209–s219.

PubMed Abstract | Google Scholar

Bhat, A., Raveesha, K. A. (2016). Antifungal activity of Pimenta dioica (L.) merril an aromatic medicinal tree. Int. J. Pharm. Pharm. Sci. 8, 92–95. doi: 10.22159/ijpps.2016v8i10.9924

CrossRef Full Text | Google Scholar

Biasi-Garbin, R. P., Demitto, F., de, O., do Amaral, R. C. R., Ferreira, M. R. A., Soares, L. A. L., et al. (2016). Antifungal potential of plant species from Brazilian caatinga against dermatophytes. Rev. Inst. Med. Trop. Sao Paulo 58:18. doi: 10.1590/S1678-9946201658018

PubMed Abstract | CrossRef Full Text | Google Scholar

Birari, R. B., Jalapure, S. S., Changrani, S. R., Shid, S. L., Tote, M. V., Habade, B. M. (2009). Antiinflammatory, analgesic and antipyretic effect of Hibiscus rosa sinesis Linn flower. Pharmacologyonline 3, 737–747.

Google Scholar

Bonilla-Jaime, H., Guadarrama-Cruz, G., Alarcon-Aguilar, F. J., Limón-Morales, O., Vazquez-Palacios, G. (2015). Antidepressant-like activity of Tagetes lucida Cav. is mediated by 5-HT1A and 5-HT2A receptors. J. Nat. Med. 69, 463–470. doi: 10.1007/s11418-015-0909-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Borrelli, F., Izzo, A. A. (2000). The plant kingdom as a source of anti-ulcer remedies. Phytother. Res. 14, 581–591. doi: 10.1002/1099-1573(200012)14:8<581::aid-ptr776>3.0.co;2-s

PubMed Abstract | CrossRef Full Text | Google Scholar

Boudreau, M. D., Beland, F. A. (2006). An evaluation of the biological and toxicological properties of Aloe barbadensis (miller), Aloe vera. J. Environ. Sci. Health C. Environ. Carcinog. Ecotoxicol. Rev. 24, 103–154. doi: 10.1080/10590500600614303

PubMed Abstract | CrossRef Full Text | Google Scholar

Boulogne, I., Germosén-Robineau, L., Ozier-Lafontaine, H., Fleury, M., Loranger-Merciris, G. (2011). TRAMIL ethnopharmalogical survey in Les Saintes (Guadeloupe, French West Indies): a comparative study. J. Ethnopharmacol. 133, 1039–1050. doi: 10.1016/j.jep.2010.11.034

PubMed Abstract | CrossRef Full Text | Google Scholar

Bourbonnais-Spear, N., Awad, R., Maquin, P., Cal, V., Vindas, P. S., Poveda, L., et al. (2005). Plant use by the Q’eqchi’ Maya of Belize in ethnopsychiatry and neurological pathology. Econ. Bot. 59, 326–336. doi: 10.1663/0013-0001(2005)059[0326:PUBTQM]2.0.CO;2

CrossRef Full Text | Google Scholar

Bourbonnais-Spear, N. (2005). Ethnobotany and ethnopharmacology of Q’eqchi" Maya medicinal plants from southern Belize used for ethnopsychiatric and neurological purposes. [MSc thesis] (Ottawa, Canada: University of Ottawa).

Google Scholar

Braga, F. G., Bouzada, M. L. M., Fabri, R. L., de O. Matos, M., Moreira, F. O., Scio, E., et al. (2007). Antileishmanial and antifungal activity of plants used in traditional medicine in Brazil. J. Ethnopharmacol. 111, 396–402. doi: 10.1016/j.jep.2006.12.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Brahmachari, G., Gorai, D., Roy, R. (2013). Argemone mexicana: chemical and pharmacological aspects. Braz. J. Pharmacongn. 23, 559–575. doi: 10.1590/S0102-695X2013005000021

CrossRef Full Text | Google Scholar

Braveman, P., Meyers, A., Schlenker, T., Wards, C. (2000). “Public health and war in Central America,” in War and Public Health. Eds. Levy, B., Sidel, V. (Washington, DC: American Public Health Association), 238–253.

Google Scholar

Brener, S., Friedman, J. (1985). Phytophotodermatitis induced by Ruta chalepensis L. Contact. Dermatitis 12, 230–232. doi: 10.1111/j.1600-0536.1985.tb01121.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Burdock, G. A., Carabin, I. G. (2009). Safety assessment of coriander (Coriandrum sativum L.) essential oil as a food ingredient. Food Chem. Toxicol. 47, 22–34. doi: 10.1016/j.fct.2008.11.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Bye, R., Linares, E. (2015). “Perspectives on ethnopharmacology in Mexico,” in Ethnopharmacology. Eds. Heinrich, M., Jäger, A. K. (West Sussex: John Wiley & Sons, Ltd, Chichester), 393–404.

Google Scholar

Bye, R., Linares, E., Estrada, E. (1995). “Biological diversity of medicinal plants in Mexico,” in Phytochemistry of medicinal plants. Eds. Arnason, J. T., Mata, R., Romeo, J. T. (New York, NY: Plenum Press), 65–82.

Google Scholar

Cabrera, G. (1994). Demographic dynamics and development: the role of population policy in Mexico. Popul. Dev. Rev. 20, 105–120. doi: 10.2307/2807942

CrossRef Full Text | Google Scholar

Cáceres, A., Cano, O., Samayoa, B., Aguilar, L. (1990). Plants used in Guatemala for the treatment of gastrointestinal disorders. 1. Screening of 84 plants against enterobacteria. J. Ethnopharmacol. 30, 55–73. doi: 10.1016/0378-8741(90)90017-N

PubMed Abstract | CrossRef Full Text | Google Scholar

Cáceres, A., Lopez, B. R., Giron, M. A., Logemann, H. (1991). Plants used in Guatemala for the treatment of dermatophytic infections. 1. Screening for antimycotic activity of 44 plant extracts. J. Ethnopharmacol. 31, 263–276. doi: 10.1016/0378-8741(91)90011-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Cáceres, A., Fletes, L., Aguilar, L., Ramirez, O., Figueroa, L., Taracena, A. M., et al. (1993a). Plants used in Guatemala for the treatment of gastrointestinal disorders. 3. Confirmation of activity against enterobacteria of 16 plants. J. Ethnopharmacol. 38, 31–38. doi: 10.1016/0378-8741(93)90076-h

PubMed Abstract | CrossRef Full Text | Google Scholar

Cáceres, A., López, B., Juárez, X., del Aguila, J., García, S. (1993b). Plants used in Guatemala for the treatment of dermatophytic infections. 2. Evaluation of antifungal activity of seven American plants. J. Ethnopharmacol. 40, 207–213. doi: 10.1016/0378-8741(93)90070-L

PubMed Abstract | CrossRef Full Text | Google Scholar

Cáceres, A., Torres, M. F., Ortiz, S., Cano, F., Jauregui, E. (1993c). Plants used in Guatemala for the treatment of gastrointestinal disorders. IV. Vibriocidal activity of five American plants used to treat infections. J. Ethnopharmacol. 39, 73–75. doi: 10.1016/0378-8741(93)90052-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Cáceres, A., Menéndez, H., Méndez, E., Cohobón, E., Samayoa, B. E., Jauregui, E., et al. (1995). Antigonorrhoeal activity of plants used in Guatemala for the treatment of sexually transmitted diseases. J. Ethnopharmacol. 48, 85–88. doi: 10.1016/0378-8741(95)01288-O

PubMed Abstract | CrossRef Full Text | Google Scholar

Cáceres, A., López, B., González, S., Berger, I., Tada, I., Maki, J. (1998). Plants used in Guatemala for the treatment of protozoal infections. I. Screening of activity to bacteria, fungi and American trypanosomes of 13 native plants. J. Ethnopharmacol. 62, 195–202. doi: 10.1016/S0378-8741(98)00140-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Cáceres, A., Rastrelli, L., De Simone, F., De Martino, G., Saturnino, C., Saturnino, P., et al. (2001). Furanocoumarins from the aerial parts of Dorstenia contrajerva. Fitoterapia 72, 376–381. doi: 10.1016/S0367-326X(00)00328-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Caceres Guido, P., Ribas, A., Gaioli, M., Quattrone, F., Macchi, A. (2015). The state of the integrative medicine in Latin America: The long road to include complementary, natural, and traditional practices in formal health systems. Eur. J. Integr. Med. 7, 5–12. doi: 10.1016/j.eujim.2014.06.010

CrossRef Full Text | Google Scholar

Cáceres, A. (2009). Vademécum Nacional de Plantas Medicinales (Guatemala: Editorial Universitaria).

Google Scholar

Cáceres, A. (2019). Integrative Medicine: A Health Paradigm of the Future. Int. J. Phytocos Nat. Ingred. 6:6. doi: 10.15171/ijpni.2019.06

CrossRef Full Text | Google Scholar

Cadena-Zamudio, J. D., Nicasio-Torres, M. P., Guerrero-Analco, J. A., Ibarra-Laclette, E. (2019). Ethnopharmacological studies of Cecropia obtusifolia (Urticaceae) and its importance in the treatment of type 2 diabetes mellitus: a mini-review. Acta Bot. Mex. 126, e1361. doi: 10.21829/abm126.2019.1361

CrossRef Full Text | Google Scholar

Calzada, F., Barbosa, E., Cedillo-Rivera, R. (2003). Antiamoebic activity of benzyl glucosinolate from Lepidium virginicum. Phyther. Res. 17, 618–619. doi: 10.1002/ptr.1210

CrossRef Full Text | Google Scholar

Calzada, F., Yépez-Mulia, L., Aguilar, A. (2006). In vitro susceptibility of Entamoeba histolytica and Giardia lamblia to plants used in Mexican traditional medicine for the treatment of gastrointestinal disorders. J. Ethnopharmacol. 108, 367–370. doi: 10.1016/j.jep.2006.05.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Campbell, L., Kaufman, T., Smith-Stark, T. C. (1986). Meso-America as a linguistic area. Language 62, 530–570. doi: 10.1353/lan.1986.0105

CrossRef Full Text | Google Scholar

Camporese, A., Balick, M. J., Arvigo, R., Esposito, R. G., Morsellino, N., Simone, F. D., et al. (2003). Screening of anti-bacterial activity of medicinal plants from Belize (Central America). J. Ethnopharmacol. 87, 103–107. doi: 10.1016/S0378-8741(03)00115-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Canales, M., Hernández, T., Caballero, J., de Vivar, A. R., Avila, G., Duran, A., et al. (2005). Informant consensus factor and antibacterial activity of the medicinal plants used by the people of San Rafael Coxcatlán, Puebla, México. J. Ethnopharmacol. 97, 429–439. doi: 10.1016/j.jep.2004.11.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Carmona, F., Angelucci, M. A., Sales, D. S., Chiaratti, T. M., Honorato, F. B., Bianchi, R. V., et al. (2013). Lippia alba (Mill.) N. E. Brown hydroethanolic extract of the leaves is effective in the treatment of migraine in women. Phytomedicine 20, 947–950. doi: 10.1016/j.phymed.2013.03.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Carrara, V. S., Cunha-Júnior, E. F., Torres-Santos, E. C., Correa, A. G., Monteiro, J. L., Demarchi, I. G., et al. (2013). Antileishmanial activity of amides from Piper amalago and synthetic analogs. Braz. J. Pharmacog. 23, 447–454. doi: 10.1590/S0102-695X2013005000022

CrossRef Full Text | Google Scholar

Carretero, M. E., López-Pérez, J. L., Abad, M. J., Bermejo, P., Tillet, S., Israel, A., et al. (2008). Preliminary study of the anti-inflammatory activity of hexane extract and fractions from Bursera simaruba (Linneo) Sarg. (Burseraceae) leaves. J. Ethnopharmacol. 116, 11–15. doi: 10.1016/j.jep.2007.10.034

PubMed Abstract | CrossRef Full Text | Google Scholar

Carvalho, A. C., Guedes, M. M., de Souza, A. L., Trevisan, M. T., Lima, A. F., Santos, F. A., et al. (2007). Gastroprotective effect of mangiferin, a xanthonoid from Mangifera indica, against gastric injury induced by ethanol and indomethacin in rodents. Planta Med. 73, 1372–1376. doi: 10.1055/s-2007-990231

PubMed Abstract | CrossRef Full Text | Google Scholar

Cassani, J., Dorantes-Barrón, M. A., Novales, M. L., Real, A. G., Estrada-Reyes, R. (2014). Anti-depressant-like effect of kaempferitrin isolated from Justicia spicigera Schltdl (Acanthaceae) in two behavior models in mice: evidence for the involvement of the serotonergic system. Molecules 19, 21442–214461. doi: 10.3390/molecules191221442

PubMed Abstract | CrossRef Full Text | Google Scholar

Castillo-Juárez, I., González, V., Jaime-Aguilar, H., Martínez, G., Linares, E., Bye, R., et al. (2009). Anti-Helicobacter pylori activity of plants used in Mexican traditional medicine for gastrointestinal disorders. J. Ethnopharmacol. 122, 402–405. doi: 10.1016/j.jep.2008.12.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Cerón, A. (2010). Los caminos del enfermo en una comunidad K’iche’ de Guatemala: Una contribución del análisis de redes al estudio de los comportamientos de búsqueda de atención en salud. Rev. Hisp. Anal. Redes Soc 18, 14–46.

Google Scholar

Céspedes, C. L., Avila, J. G., Martínez, A., Serrato, B., Calderón-Mugica, J. C., Salgado-Garciglia, R. (2006). Antifungal and antibacterial activities of Mexican tarragon (Tagetes lucida). J. Agric. Food Chem. 54, 3521–3527. doi: 10.1021/jf053071w

PubMed Abstract | CrossRef Full Text | Google Scholar

Chagas-Paula, D. A., Oliveira, R. B., da Silva, V. C., Gobbo-Neto, L., Gasparoto, T. H., Campanelli, A. P., et al. (2011). Chlorogenic acids from Tithonia diversifolia demonstrate better anti-inflammatory effect than indomethacin and its sesquiterpene lactones. J. Ethnopharmacol. 136, 355–362. doi: 10.1016/j.jep.2011.04.067

PubMed Abstract | CrossRef Full Text | Google Scholar

Chary, A., Flood, D., Austad, K., Colom, M., Hawkins, J., Cnop, K., et al. (2018). Accompanying indigenous Maya patients with complex medical needs: A patient navigation system in rural Guatemala. Healthcare 6, 144–149. doi: 10.1016/j.hjdsi.2017.08.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Chauhan, A., Ruby, K. M., Shori, A., Dwivedi, J. (2012). Solanum nigrum with dynamic therapeutic role: A review. Int. J. Pharm. Sci. Rev. Res. 15, 65–71.

Google Scholar

Chen, C.-C., Ng, W.-W., Chang, F.-Y., Lee, S.-D. (1999). Magnesium citrate–bisacodyl regimen proves better than castor oil for colonoscopic preparation. J. Gastroenterol. Hepatol. 14, 1219–1222. doi: 10.1046/j.1440-1746.1999.02032.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Chibli, L. A., Rodrigues, K. C. M., Gasparetto, C. M., Pinto, N. C. C., Fabri, R. L., Scio, E., et al. (2014). Anti-inflammatory effects of Bryophyllum pinnatum (Lam.) Oken ethanol extract in acute and chronic cutaneous inflammation. J. Ethnopharmacol. 154, 330–338. doi: 10.1016/j.jep.2014.03.035

PubMed Abstract | CrossRef Full Text | Google Scholar

Chinchilla-Carmona, M., Valerio-Campos, I., Sánchez-Porras, R., Bagnarello-Madrigal, V., Martínez-Esquivel, L., González-Paniagua, A., et al. (2014). Actividad contra Leishmania sp. (Kinetoplastida: Trypanosomatidae) de plantas en una Reserva Biológica de Costa Rica. Rev. Biol. Trop. 62, 1229–1240. doi: 10.15517/rbt.v62i3.12377

PubMed Abstract | CrossRef Full Text | Google Scholar

Cho, J.-H., Lee, C.-H., Lee, H.-S. (2005). Antimicrobial activity of quinoline derivatives isolated from Ruta chalepensis toward human intestinal bacteria. J. Microbiol. Biotechnol. 15, 646–651.

Google Scholar

Christensen, R., Bartels, E. M., Astrup, A., Bliddal, H. (2008). Symptomatic efficacy of avocado–soybean unsaponifiables (ASU) in osteoarthritis (OA) patients: a meta-analysis of randomized controlled trials. Osteoarthr. Cartil. 16, 399–408. doi: 10.1016/j.joca.2007.10.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Christian, E. O., Okwesili, F. C. N., Parker, E. J., Okechukwu, P. C. U. (2014). Acute toxicity investigation and anti-diarrhoeal effect of the chloroform-methanol extract of the leaves of Persea americana. Iran. J. Pharm. Res. 13, 651–658.

PubMed Abstract | Google Scholar

Clark, J. E. (1991). “The beginnings of Mesoamerica: apologia for the Soconusco early Formative,” in The formation of complex society in southeastern Mesoamerica. Ed. Fowler, W. R., Jr (Boca Raton: CRC Press).

Google Scholar

CMMM (Concejo Mayor de Médicos Mayas por Nacimiento) (2016). Raxnaq’il Nuk’aslemal, Bienestar en Nuestras Vidas: Medicina Maya en Guatemala (Editorial Cholsamaj: Guatemala).

Google Scholar

Coe, M. D., Houston, S. (2015). The Maya. 9th edition (New York: Thames & Hudson).

Google Scholar

Coe, M. D., Koontz, R. (2013). Mexico: from the Olmecs to the Aztecs. 7th edition (London: Thames & Hudson).

Google Scholar

Colon-Gonzalez, M. C., El Rayess, F., Guevara, S., Anandarajah, G. (2015). Successes, challenges and needs regarding rural health medical education in continental Central America: a literature review and narrative synthesis. Rural Remote Health 15, 3361.

PubMed Abstract | Google Scholar

Comerford, K. B., Ayoob, K. T., Murray, R. D., Atkinson, S. A. (2016). The Role of avocados in maternal diets during the periconceptional period, pregnancy, and lactation. Nutrients 8, 313. doi: 10.3390/nu8050313

CrossRef Full Text | Google Scholar

Comerford, S. C. (1996). Medicinal plants of two Mayan healers from San Andrés, Petén, Guatemala. Econ. Bot. 50, 327–336. doi: 10.1007/BF02907342

CrossRef Full Text | Google Scholar

Compadre, C. M., Robbins, E. F., Kinghorn, A. D. (1986). The intensely sweet herb, Lippia dulcis Trev.: Historical uses, field inquiries, and constituents. J. Ethnopharmacol. 15, 89–106. doi: 10.1016/0378-8741(86)90105-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Cortez-Navarrete, M., Martínez-Abundis, E., Pérez-Rubio, K. G., González-Ortiz, M., Méndez-Del Villar, M. (2018). Momordica charantia Administration Improves Insulin Secretion in Type 2 Diabetes Mellitus. J. Med. Food. 21, 672–677. doi: 10.1089/jmf.2017.0114

PubMed Abstract | CrossRef Full Text | Google Scholar

Corzo-Martínez, M., Corzo, N., Villamiel, M. (2007). Biological properties of onions and garlic. Trends Food Sci. Technol. 18, 609–625. doi: 10.1016/j.tifs.2007.07.011

CrossRef Full Text | Google Scholar

Costa, C. T. C., Bevilaqua, C. M. L., Morais, S. M., Camurça-Vasconcelos, A. L. F., Maciel, M. V., Braga, R. R., et al. (2010). Anthelmintic activity of Cocos nucifera L. on intestinal nematodes of mice. Res. Vet. Sci. 88, 101–103. doi: 10.1016/j.rvsc.2009.05.008

CrossRef Full Text | Google Scholar

Costa, G. M., Schenkel, E. P., Reginatto, F. H. (2011). Chemical and pharmacological aspects of the genus Cecropia. Nat. Prod. Commun. 6, 913–920. doi: 10.1177/1934578X1100600637

PubMed Abstract | CrossRef Full Text | Google Scholar

Cruz, E. C., Andrade-Cetto, A. (2015). Ethnopharmacological field study of the plants used to treat type 2 diabetes among the Cakchiquels in Guatemala. J. Ethnopharmacol. 159, 238–244. doi: 10.1016/j.jep.2014.11.021

PubMed Abstract | CrossRef Full Text | Google Scholar

da Silva Arrigo, J., Balen, E., Júnior, U. L., da Silva Mota, J., Iwamoto, R. D., Barison, A., et al. (2016). Anti-nociceptive, anti-hyperalgesic and anti-arthritic activity of amides and extract obtained from Piper amalago in rodents. J. Ethnopharmacol. 179, 101–109. doi: 10.1016/j.jep.2015.12.046

PubMed Abstract | CrossRef Full Text | Google Scholar

da Silva, C. R., Oliveira, M. B. N., Motta, E. S., de Almeida, G. S., Varanda, L. L., de Pádula, et al. (2010). Genotoxic and cytotoxic safety evaluation of papain (Carica papaya L.) using in vitro assays. J. Biomed. Biotechnol. 2010:197898. doi: 10.1155/2010/197898

PubMed Abstract | CrossRef Full Text | Google Scholar

da Silva, M. G. C., Amorim, R. N. L., Câmara, C. C., Fontenele Neto, J. D., Soto-Blanco, B. (2014). Acute and sub-chronic toxicity of aqueous extracts of Chenopodium ambrosioides leaves in rats. J. Med. Food 17, 979–984. doi: 10.1089/jmf.2013.0134

PubMed Abstract | CrossRef Full Text | Google Scholar

Dat, A. D., Poon, F., Pham, K. B., Doust, J. (2012). Aloe vera for treating acute and chronic wounds. Cochrane Database Syst. Rev. 15, CD008762. doi: 10.1002/14651858.CD008762.pub2

CrossRef Full Text | Google Scholar

Dawilai, S., Muangnoi, C., Praengamthanachoti, P., Tuntipopipat, S. (2013). Anti-inflammatory activity of bioaccessible fraction from Eryngium foetidum leaves. Biomed. Res. Int. 2013, 958567. doi: 10.1155/2013/958567

PubMed Abstract | CrossRef Full Text | Google Scholar

de Alencar, N. M. N., Pinheiro, R. S. P., de Figueiredo, I. S. T., Luz, P. B., Freitas, L. B. N., de Souza, T., et al. (2015). The preventive effect on ethanol-induced gastric lesions of the medicinal plant Plumeria rubra: involvement of the latex proteins in the NO/cGMP/K ATP signaling pathway. Evid. Based Complement. Alternat. Med. 2015, 706782. doi: 10.1155/2015/706782

PubMed Abstract | CrossRef Full Text | Google Scholar

De Almeida, C. L. F., Brito, S. A., De Santana, T. I., Costa, H. B. A., De Carvalho Júnior, C. H. R., Da Silva, M. V., et al. (2017). Spondias purpurea L. (Anacardiaceae): Antioxidant and antiulcer activities of the leaf hexane extract. Oxid. Med. Cell. Longev. 2017, 6593073. doi: 10.1155/2017/6593073

PubMed Abstract | CrossRef Full Text | Google Scholar

De Pinho, J. P. M., Silva, A. S. B., Pinheiro, B. G., Sombra, I., de Carvalho, J., Lahlou, S., et al. (2012). Antinociceptive and antispasmodic effects of the essential oil of Ocimum micranthum: potential anti-inflammatory properties. Planta Med. 78, 681–685. doi: 10.1055/s-0031-1298372

PubMed Abstract | CrossRef Full Text | Google Scholar

De Sousa Santos, B. (2010). Decolonizar el saber, reinventar el poder (Montevideo: Ediciones Trilce).

Google Scholar

De Sousa Santos, B. (2011). Epistemologías del Sur. Rev. Int. Filos. Iberoam. Teor. Soc 16, 17–39.

Google Scholar

de Toledo, S. J., Ambrósio, R. S., Borges, H. C., Manfrim, V., Cerri, G. D., Cruz, K. A., et al. (2014). In vitro leishmanicidal activities of sesquiterpene lactones from Tithonia diversifolia against Leishmania braziliensis promastigotes and amastigotes. Molecules 19, 6070–6079. doi: 10.3390/molecules19056070

PubMed Abstract | CrossRef Full Text | Google Scholar

Dewick, P. M. (2002). Medicinal Natural Products. A Biosynthetic Approach. 2nd edition (Chichester: John Wiley & Sons Ltd).

Google Scholar

Diehl, R. A. (2004). The Olmecs: America’s first civilization (London: Thames & Hudson).

Google Scholar

Dinda, B., Das, N., Dinda, S., Dinda, M., SilSarma, I. (2015). The genus Sida L. – A traditional medicine: Its ethnopharmacological, phytochemical and pharmacological data for commercial exploitation in herbal drugs industry. J. Ethnopharmacol. 176, 135–176. doi: 10.1016/j.jep.2015.10.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Doan, L. G. (2004). Ricin: Mechanism of toxicity, clinical manifestations, and vaccine development. A review. J. Toxicol. Clin. Toxicol. 42, 201–208. doi: 10.1081/CLT-120030945

PubMed Abstract | CrossRef Full Text | Google Scholar

Domínguez-Vigil, I. G., Camacho-Corona, M. D. R., Heredia-Rojas, J. A., Vargas-Villarreal, J., Rodríguez-De La Fuente, A. O., Heredia-Rodríguez, O., et al. (2015). Anti-giardia activity of hexane extract of Citrus aurantifolia (Christim) swingle and some of its constituents. Afr. J. Tradit. Complement. Altern. Med. 12, 55–59. doi: 10.4314/ajtcam.v12i2.10

CrossRef Full Text | Google Scholar

Du Dat, D., Ham, N. N., Khac, D. H., Lam, N. T., Son, P. T., van Dau, N., et al. (1992). Studies on the individual and combined diuretic effects of four Vietnamese traditional herbal remedies (Zea mays, Imperata cylindrica, Plantago major and Orthosiphon stamineus). J. Ethnopharmacol. 36, 225–231. doi: 10.1016/0378-8741(92)90048-V

PubMed Abstract | CrossRef Full Text | Google Scholar

Dutok, C. M. S., Berenguer-Rivas, C. A., Rodríguez-Leblanch, E., Pérez-Jackson, L., Chil-Nuñez, I., Escalona-Arranz, J. C., et al. (2015). Acute toxicity and dermal and eye irritation of the aqueous and hydroalcoholic extracts of the seeds of “zapote” Pouteria mammosa (L.) Cronquist. Sci. World J. 2015, 642906. doi: 10.1155/2015/642906

CrossRef Full Text | Google Scholar

Eguale, T., Tilahun, G., Debella, A., Feleke, A., Makonnen, E. (2007). In vitro and in vivo anthelmintic activity of crude extracts of Coriandrum sativum against Haemonchus contortus. J. Ethnopharmacol. 110, 428–433. doi: 10.1016/j.jep.2006.10.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Ekpenyong, C. E., Akpan, E., Nyoh, A. (2015). Ethnopharmacology, phytochemistry, and biological activities of Cymbopogon citratus (DC.) Stapf extracts. Chin. J. Nat. Med. 13, 321–337. doi: 10.1016/S1875-5364(15)30023-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Elufioye, T. O., Alatise, O. I., Fakoya, F. A., Agbedahunsi, J. M., Houghton, P. J. (2009). Toxicity studies of Tithonia diversifolia A. Gray (Asteraceae) in rats. J. Ethnopharmacol. 122, 410–415. doi: 10.1016/j.jep.2008.12.007

PubMed Abstract | CrossRef Full Text | Google Scholar

EMA/HMPC (2008). Assessment report on Foeniculum vulgare Miller. European medicine agency, Committee on Herbal Medicinal Products, EMA/HMPC: 137426. London, UK: European Medicines Agency.

Google Scholar

EMA/HMPC (2017). Assessment report on Artemisia absinthium L., herba. European medicine agency, Committee on Herbal Medicinal Products, EMA/HMPC: 751484. London, UK: European Medicines Agency.

Google Scholar

Escalona-Arranz, J. C., Perez-Rosés, R., Rodríguez-Amado, J., Morris-Quevedo, H. J., Mwasi, L. B., Cabrera-Sotomayor, O., et al. (2016). Antioxidant and toxicological evaluation of a Tamarindus indica L. leaf fluid extract. Nat. Prod. Res. 30, 456–459. doi: 10.1080/14786419.2015.1019350

PubMed Abstract | CrossRef Full Text | Google Scholar

Estrada-Soto, S., Sánchez-Recillas, A., Navarrete-Vázquez, G., Castillo-España, P., Villalobos-Molina, R., Ibarra-Barajas, M. (2012). Relaxant effects of Artemisia ludoviciana on isolated rat smooth muscle tissues. J. Ethnopharmacol. 139, 513–518. doi: 10.1016/j.jep.2011.11.041

PubMed Abstract | CrossRef Full Text | Google Scholar

Evangeline, R. M., Murugan, N., Parveen Kumar, P., Nimal Christhudas, I. V. S. (2015). In vitro studies on A-Gucosidase inhibition, antioxidant and free radical scavenging properties of Tecoma stans L. Int. J. Pharm. Pharm. Sci. 7, 44–49.

Google Scholar

Evans, F. J., Taylor, S. E. (1983). Pro-inflammatory, tumour-promoting and anti-tumour diterpenes of the plant families Euphorbiaceae and Thymelaeaceae. Fortschr. Chem. Org. Naturst. 44, 1–99. doi: 10.1007/978-3-7091-8714-2_1

PubMed Abstract | CrossRef Full Text | Google Scholar

F̈rer, K., Sim.es-Ẅst, A. P., Von Mandach, U., Hamburger, M., Potterat, O. (2016). Bryophyllum pinnatum and related species used in anthroposophic medicine: constituents, pharmacological activities, and clinical efficacy. Planta Med. 82, 930–941. doi: 10.1055/s-0042-106727

PubMed Abstract | CrossRef Full Text | Google Scholar

Fandohan, P., Gnonlonfin, B., Laleye, A., Gbenou, J. D., Darboux, R., Moudachirou, M. (2008). Toxicity and gastric tolerance of essential oils from Cymbopogon citratus, Ocimum gratissimum and Ocimum basilicum in Wistar rats. Food Chem. Toxicol. 46, 2493–2497. doi: 10.1016/j.fct.2008.04.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Favela-Hernández, J.M., González-Santiago, O., Ramírez-Cabrera, M.A., Esquivel-Ferriño, P.C., Camacho-Corona Mdel, R. (2016). Chemistry and Pharmacology of Citrus sinensis. Molecules 21, 247. doi: 10.3390/molecules21020247

CrossRef Full Text | Google Scholar

FEUM (2013). Farmacopea herbolaria de los Estados Unidos Mexicanos, segunda edición (Mexico City: Secretaria de Salud, Comisión Permanente de la Farmacopea de los Estados Unidos Mexicanos).

Google Scholar

Flores Alvarado, A., Morán Zenteno, J. A. (1989). Effects of the health care model of the Mexican Social Security Institute-COPLAMAR program on the health status of the underprivileged rural population of Mexico. Salud Publica Mex. 31, 745–756.

PubMed Abstract | Google Scholar

Flores, W., Ruano, A., Funchal, D. (2009). Social Participation within a Context of Political Violence: Implications for the Promotion and Exercise of the Right to Health in Guatemala. Health Hum. Rights 11, 37–48. doi: 10.2307/40285216

PubMed Abstract | CrossRef Full Text | Google Scholar

Fort, M. P., Grembowski, D. E., Verdugo, J. C., Morales, L. C., Arriaga, C. A., Mercer, M. A., et al. (2011). Implementation and progress of an inclusive primary health care model in Guatemala: Coverage, quality, and utilization. Pan Am. J. Public Health 30, 217–224. doi: 10.1590/S1020-49892011000900005 (Revista panamericana de salud pública).

CrossRef Full Text | Google Scholar

Fortis-Barrera, M. A., Alarcón-Aguilar, F. J., Becerril-García, A., Flores-Sáenz, J. L. E., Almanza-Pérez, J. C., García-Lorenzana, M., et al. (2019). Mechanism of the hypoglycemic activity and hepatoprotective effect of the aqueous extract of Cecropia obtusifolia Bertol. J. Med. Food. 1–10. doi: 10.1089/jmf.2019.0126 In press.

CrossRef Full Text | Google Scholar

Foster, G. M. (1994). Hippocrates" Latin American legacy: humoral medicine in the New World (Amsterdam: Gordon and Breach).

Google Scholar

Frei, B., Baltisberger, M., Sticher, O., Heinrich, M. (1998). Medical ethnobotany of the Zapotecs of the Isthmus-Sierra (Oaxaca, Mexico): Documentation and assessment of indigenous uses. J. Ethnopharmacol. 62, 149–165. doi: 10.1016/S0378-8741(98)00051-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Frei, B. (1997). Medical ethnobotany of the Isthmus-Sierra Zapotecs (Oaxaca, Mexico) and biological-phytochemical investigation of selected medicinal plants. [PhD dissertation] (Zurich, Switzerland: Swiss Federal Institute of Technology).

Google Scholar

Frenk, J. (2006). Bridging the divide: global lessons from evidence-based health policy in Mexico. Lancet 368, 954–961. doi: 10.1016/S0140-6736(06)69376-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Gabriela, G. C., Javier, A. A., Elisa, V.A., Gonzalo, V.P., Herlinda, B.J. (2012). Antidepressant-like effect of Tagetes lucida Cav. extract in rats: involvement of the serotonergic system. Am. J. Chin. Med. 40, 753–768. doi: 10.1142/S0192415X12500565

PubMed Abstract | CrossRef Full Text | Google Scholar

Gaire, B. P., Subedi, L. (2013). A review on the pharmacological and toxicological aspects of Datura stramonium L. J. Integr. Med. 11, 73–79. doi: 10.3736/jintegrmed2013016

PubMed Abstract | CrossRef Full Text | Google Scholar

Ganguly, A., Al Mahmud, Z., Kumar Saha, S., Abdur Rahman, S. M. (2016). Evaluation of antinociceptive and antidiarrhoeal properties of Manilkara zapota leaves in Swiss albino mice. Pharm. Biol. 54, 1413–1419. doi: 10.3109/13880209.2015.1103757

PubMed Abstract | CrossRef Full Text | Google Scholar

García-Hernández, K. Y., Vibrans, H., Rivas-Guevara, M., Aguilar-Contreras, A. (2015). This plant treats that illness? The hot–cold system and therapeutic procedures mediate medicinal plant use in San Miguel Tulancingo, Oaxaca, Mexico. J. Ethnopharmacol. 163, 12–30. doi: 10.1016/j.jep.2015.01.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Garrido, G., Rodeiro, I., Hernndez, I., Garca, G., Prez, G., Merino, N., et al. (2009). In vivo acute toxicological studies of an antioxidant extract from Mangifera indica L. (Vimang). Drug Chem. Toxicol. 32, 53–58. doi: 10.1080/01480540802432551

PubMed Abstract | CrossRef Full Text | Google Scholar

Geck, M. S., Reyes García, A. J., Casu, L., Leonti, M. (2016). Acculturation and ethnomedicine: a regional comparison of medicinal plant knowledge among the Zoque of southern Mexico. J. Ethnopharmacol. 187, 146–159. doi: 10.1016/j.jep.2016.04.036

PubMed Abstract | CrossRef Full Text | Google Scholar

Geck, M. S., Cabras, S., Casu, L., Reyes García, A. J., Leonti, M. (2017). The taste of heat: How humoral qualities act as a cultural filter for chemosensory properties guiding herbal medicine. J. Ethnopharmacol. 198, 499–515. doi: 10.1016/j.jep.2017.01.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Germosén-Robineau, L. (2005). Farmacopea Vegetal Caribeña. 2nd edition (Santo Domingo: TRAMIL).

Google Scholar

Ghazghazi, H., Aouadhi, C., Weslati, M., Trakhna, F., Maaroufi, A., Hasnaoui, B. (2015). Chemical composition of Ruta chalepensis leaves essential oil and variation in biological activities between leaves, stems and roots methanolic extracts. J. Essent. Oil Bear. Plants 18, 570–581. doi: 10.1080/0972060X.2014.905757

CrossRef Full Text | Google Scholar

Ghisalberti, E. L. (2000). Lantana camara L. (Verbenaceae). Fitoterapia 71, 467–486. doi: 10.1016/S0367-326X(00)00202-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Ghosh, S., Samanta, A., Mandal, N. B., Bannerjee, S., Chattopadhyay, D. (2012). Evaluation of the wound healing activity of methanol extract of Pedilanthus tithymaloides (L.) Poit leaf and its isolated active constituents in topical formulation. J. Ethnopharmacol. 142, 714–722. doi: 10.1016/j.jep.2012.05.048

PubMed Abstract | CrossRef Full Text | Google Scholar

Giannetti, A. A. M., Pin, A. R., Pietro, N. A. S., de Oliveira, H. C., Mendes-Giannini, J. S., Alecio, A. C., et al. (2010). Composition and antifungal activity against Candida albicans, Candida parapsilosis, Candida krusei and Cryptococcus neoformans of essential oils from leaves of Piper and Peperomia species. J. Med. Plant Res. 4, 1810–1814. doi: 10.5897/JMPR09.303

CrossRef Full Text | Google Scholar

Giordani, M. A., Collicchio, T. C. M., Ascêncio, S. D., de Oliveira Martins, D. T., Balogun, S. O., Bieski, I. G. C., et al. (2015). Hydroethanolic extract of the inner stem bark of Cedrela odorata has low toxicity and reduces hyperglycemia induced by an overload of sucrose and glucose. J. Ethnopharmacol. 162, 352–361. doi: 10.1016/j.jep.2014.12.059

PubMed Abstract | CrossRef Full Text | Google Scholar

Giovannini, P., Howes, M. J. R. (2017). Medicinal plants used to treat snakebite in Central America: Review and assessment of scientific evidence. J. Ethnopharmacol. 199, 240–256. doi: 10.1016/j.jep.2017.02.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Giovannini, P., Howes, M. J. R., Edwards, S. E. (2016). Medicinal plants used in the traditional management of diabetes and its sequelae in Central America: a review. J. Ethnopharmacol. 184, 58–71. doi: 10.1016/j.jep.2016.02.034

PubMed Abstract | CrossRef Full Text | Google Scholar

Goetz, P. (2014). Citrus limon (L.) Burm. f. (Rutacées) citronnier. Phytothérapie 12, 116–121. doi: 10.1007/s10298-014-0854-6

CrossRef Full Text | Google Scholar

Gómez, J., Jiménez, J., Martner, R. (2017). Consensos y Conflictos en la Cultura Tributaria de America Latina (Santiago: Comisión Económica para América Latina y el Caribe).

Google Scholar

Gomez-Beloz, A., Rucinski, J. C., Balick, M. J., Tipton, C. (2003). Double incision wound healing bioassay using Hamelia patens from El Salvador. J. Ethnopharmacol. 88, 169–173. doi: 10.1016/S0378-8741(03)00209-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Gómez-Dantés, O., Sesma, S., Becerril, V. M., Knaul, F. M., Arreola, H., Frenk, J. (2011a). Sistema de salud de México. Salud Publica Mex. 53, s220–s232.

PubMed Abstract | Google Scholar

Goméz-Dantés, H., Castro, V., Franco-Marina, F., Bedregal, P., García, J. R., Espinoza, A., et al. (2011b). La carga de la enfermedad en países de América Latina. Salud Publica Mex. 53, s72–s77.

PubMed Abstract | Google Scholar

Gómez-Dantés, H., Fullman, N., Lamadrid-Figueroa, H., Cahuana-Hurtado, L., Darney, B., Avila-Burgos, L., et al. (2016). Dissonant health transition in the states of Mexico 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet 388, 2386–2402. doi: 10.1016/S0140-6736(16)31773-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Gonçalo, S., Correia, C., Couto, J. S., Gonçalo, M. (1989). Contact and photocontact dermatitis from Ruta chalepensis contact. Dermatitis 21, 200–201. doi: 10.1111/j.1600-0536.1989.tb04740.x

CrossRef Full Text | Google Scholar

Gonzales, J., Benavides, V., Rojas, R., Pino, J. (2007). Embryotoxic and teratogenic effect of Ruta chalepensis L. «rue», in mouse (Mus musculus). Rev. Peru. Biol. 13, 223–225.

Google Scholar

Gonzalez-Trujano, M. E., Carrera, D., Ventura-Martinez, R., Cedillo-Portugal, E., Navarrete, A. (2006). Neuropharmacological profile of an ethanol extract of Ruta chalepensis L. in mice. J. Ethnopharmacol. 106, 129–135. doi: 10.1016/j.jep.2005.12.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Görnemann, T., Nayal, R., Pertz, H. H., Melzig, M. F. (2008). Antispasmodic activity of essential oil from Lippia dulcis Trev. J. Ethnopharmacol. 117, 166–169. doi: 10.1016/j.jep.2008.01.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Gracioso, J. S., Paulo, M. Q., Hiruma Lima, C. A., Brito, A. R. M. S. (1998). Natural products: antinociceptive effect in mice of a hydroalcoholic extract of Neurolaena lobata (L.) R.Br. ex Cass. and its organic fractions. J. Pharm. Pharmacol. 50, 1425–1429. doi: 10.1111/j.2042-7158.1998.tb03370.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Graz, B., Diallo, D., Falquet, J., Willcox, M., Giani, S. (2005). Screening of traditional herbal medicine: first, do a retrospective study, with correlation between diverse treatments used and reported patient outcome. J. Ethnopharmacol. 101, 338–339. doi: 10.1016/j.jep.2005.07.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Graz, B., Elisabetsky, E., Falquet, J. (2007). Beyond the myth of expensive clinical study: assessment of traditional medicines. J. Ethnopharmacol. 113, 382–386. doi: 10.1016/j.jep.2007.07.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Groark, K. P. (2005). Vital warmth and well-being: steambathing as household therapy among the Tzeltal and Tzotzil Maya of highland Chiapas, Mexico. Soc Sci. Med. 61, 785–795. doi: 10.1016/j.socscimed.2004.08.044

PubMed Abstract | CrossRef Full Text | Google Scholar

Grzanna, R., Lindmark, L., Frondoza, C. G. (2005). Ginger—An Herbal Medicinal Product with Broad Anti-Inflammatory Actions. J. Med. Food 8, 125–132. doi: 10.1089/jmf.2005.8.125

PubMed Abstract | CrossRef Full Text | Google Scholar

Guadarrama-Cruz, G., Alarcon-Aguilar, F. J., Lezama-Velasco, R., Vazquez-Palacios, G., Bonilla-Jaime, H. (2008). Antidepressant-like effects of Tagetes lucida Cav. in the forced swimming test. J. Ethnopharmacol. 120, 277–281. doi: 10.1016/j.jep.2008.08.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Guadarrama-Cruz, G., Alarcón-Aguilar, F. J., Vega-Avila, E., Vázquez-Palacios, G., Bonilla-Jaime, H. (2012). Antidepressant-like effect of Tagetes lucida Cav. extract in rats: involvement of the serotonergic system. Am. J. Chin. Med. 40, 753–768. doi: 10.1142/S0192415X12500565

PubMed Abstract | CrossRef Full Text | Google Scholar

Gupta, P., Vasudeva, N. (2010). In vitro antiplasmodial and antimicrobial potential of Tagetes erecta roots. Pharm. Biol. 48, 1218–1223. doi: 10.3109/13880201003695142

PubMed Abstract | CrossRef Full Text | Google Scholar

Gupta, M. P., Arias, T. D., Williams, N. H., Bos, R., Tattje, D. H. E. (1985). Safrole, the main component of the essential oil from Piper auritum of Panama. J. Nat. Prod. 48, 330. doi: 10.1021/np50038a026

CrossRef Full Text | Google Scholar

Gutiérrez, R. M. P., Mitchell, S., Solis, R. V. (2008). Psidium guajava: A review of its traditional uses, phytochemistry and pharmacology. J. Ethnopharmacol. 117, 1–27. doi: 10.1016/j.jep.2008.01.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Guzmán-Gutiérrez, S. L., Reyes-Chilpa, R., Bonilla-Jaime, H. (2014). Medicinal plants for the treatment of “nervios”, anxiety, and depression in Mexican Traditional Medicine. Rev. Bras. Farmacogn. 24, 591–608. doi: 10.1016/j.bjp.2014.10.007

CrossRef Full Text | Google Scholar

Habicht, S. D., Ludwig, C., Yang, R. Y., Krawinkel, M. B. (2014). Momordica charantia and type 2 diabetes: From in vitro to human studies. Curr. Diabetes Rev. 10, 48–60. doi: 10.2174/1573399809666131126152044

PubMed Abstract | CrossRef Full Text | Google Scholar

Haddouchi, F., Chaouche, T. M., Zaouali, Y., Ksouri, R., Attou, A., Benmansour, A. (2013). Chemical composition and antimicrobial activity of the essential oils from four Ruta species growing in Algeria. Food Chem. 141, 253–258. doi: 10.1016/j.foodchem.2013.03.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Hammarström, H., Forkel, R., Haspelmath, M., Bank, S. (2016). Glottolog 2.7 (Jena: Max Planck Institute for the Science of Human History).

Google Scholar

Harris, J. C., Cottrell, S., Plummer, S., Lloyd, D. (2001). Antimicrobial properties of Allium sativum (garlic). Appl. Microbiol. Biotechnol. 57, 282–286. doi: 10.1007/s002530100722

PubMed Abstract | CrossRef Full Text | Google Scholar

Hasanudin, K., Hashim, P., Mustafa, S. (2012). Corn silk (Stigma Maydis) in Healthcare: A Phytochemical and pharmacological review. Molecules 17, 9697–9715. doi: 10.3390/molecules17089697

PubMed Abstract | CrossRef Full Text | Google Scholar

Hashemi, S. R., Zulkifli, I., Bejo, M. H., Farida, A., Somchit, M. N. (2008). Acute toxicity study and phytochemical screening of selected herbal aqueous extract in broiler chickens. Int. J. Pharmacol. 4, 352–360. doi: 10.3923/ijp.2008.352.360

CrossRef Full Text | Google Scholar

Heidari, B., Sajjadi, S. E., Minaiyan, M. (2016). Effect of Coriandrum sativum hydroalcoholic extract and its essential oil on acetic acid- induced acute colitis in rats. Avicenna J. Phytomed. 6, 205–214.

PubMed Abstract | Google Scholar

Heimbach, J. T., Marone, P. A., Hunter, J. M., Nemzer, B. V., Stanley, S. M., Kennepohl, E. (2010). Safety studies on products from whole coffee fruit. Food Chem. Toxicol. 48, 2517–2525. doi: 10.1016/j.fct.2010.06.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Heinrich, M., Ankli, A., Frei, B., Weimann, C., Sticher, O. (1998). Medicinal plants in Mexico: healers’ consensus and cultural importance. Soc Sci. Med. 47, 1863–1875. doi: 10.1016/s0277-9536(98)00181-6

CrossRef Full Text | Google Scholar

Heinrich, M., Frei Haller, B., Leonti, M. (2014). A perspective on natural products research and ethnopharmacology in Mexico: the eagle and the serpent on the prickly pear cactus. J. Nat. Prod. 77, 678–689. doi: 10.1021/np4009927

PubMed Abstract | CrossRef Full Text | Google Scholar

Heinrich, M. (1989). Ethnobotanik der Tieflandmixe (Oaxaca, Mexico) und phytochemische Untersuchung von Capraria biflora L. (Scophulariaceae) (Berlin: J. Cramer).

Google Scholar

Heinrich, M. (1998). “Plants as antidiarrhoeals in medicine and diet,” in Plants for Food and Medicine, proceedings from a joint meeting of the Society for Economic Botany and the International Society for Ethnopharmacology. Eds. Prendergast, H. D. V., Etkin, N. L., Harris, D. R., Houghton, P. J. (Kew: Royal Botanic Gardens), 17–30.

Google Scholar

Hennebelle, T., Sahpaz, S., Joseph, H., Bailleul, F. (2008). Ethnopharmacology of Lippia alba. J. Ethnopharmacol. 116, 211–222. doi: 10.1016/j.jep.2007.11.044

PubMed Abstract | CrossRef Full Text | Google Scholar

Herrera-Arellano, A., Aguilar-Santamaría, L., García-Hernández, B., Nicasio-Torres, P., Tortoriello, J. (2004). Clinical trial of Cecropia obtusifolia and Marrubium vulgare leaf extracts on blood glucose and serum lipids in type 2 diabetics. Phytomedicine 11, 561–566. doi: 10.1016/j.phymed.2004.01.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Herrera-Ruiz, M., Zamilpa, A., González-Cortazar, M., Reyes-Chilpa, R., León, E., García, M. P., et al. (2011). Antidepressant effect and pharmacological evaluation of standardized extract of flavonoids from Byrsonima crassifolia. Phytomedicine 18, 1255–1261. doi: 10.1016/j.phymed.2011.06.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Hitziger, M. O., Heinrich, M., Edwards, P., Pöll, E., Lopez, M., Krütli, P. (2016). Maya phytomedicine in Guatemala – can cooperative research change ethnopharmacological paradigms? J. Ethnopharmacol. 186, 61–72. doi: 10.1016/j.jep.2016.03.040

PubMed Abstract | CrossRef Full Text | Google Scholar

Hitziger, M., Berger-González, M., Gharzouzi, E., Ochaíta Santizo, D., Solis Miranda, R., Aguilar Ferro, A. I., et al. (2017). Patient-centered boundary mechanisms to foster intercultural partnerships in health care: a case study in Guatemala. J. Ethnobiol. Ethnomed. 13, 44. doi: 10.1186/s13002-017-0170-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Homedes, N., Ugalde, A. (2009). Twenty-five years of convoluted health reforms in Mexico. PloS Med. 6, e1000124. doi: 10.1371/journal.pmed.1000124

PubMed Abstract | CrossRef Full Text | Google Scholar

Hör, M., Rimpler, H., Heinrich, M. (1995). Inhibition of intestinal chloride secretion by proanthocyanidins from Guazuma ulmifolia. Planta Med. 61, 208–212. doi: 10.1055/s-2006-958057

PubMed Abstract | CrossRef Full Text | Google Scholar

Hosseinzadeh, S., Ghalesefidi, M. J., Azami, M., Mohaghegh, M. A., Hejazi, S. H., Ghomashlooyan, M. (2016). In vitro and in vivo anthelmintic activity of seed extract of Coriandrum sativum compared to Niclosamid against Hymenolepis nana infection. J. Parasitol. Dis. 40, 1307–1310. doi: 10.1007/s12639-015-0676-y

CrossRef Full Text | Google Scholar

Hubert, D. J., Céline, N., Michel, N., Gogulamudi, V. R., Florence, N. T., Johnson, B. N., et al. (2013). In vitro leishmanicidal activity of some Cameroonian medicinal plants. Exp. Parasitol. 134, 304–308. doi: 10.1016/j.exppara.2013.03.023

PubMed Abstract | CrossRef Full Text | Google Scholar

Hunn, E. S. (2008). A Zapotec natural history: trees, herbs, and flowers, birds, beasts, and bugs in the life of San Juan Gbëë (Tucson: University of Arizona Press).

Google Scholar

Isbister, G. K., Oakley, P., Dawson, A. H., Whyte, I. M. (2003). Presumed angel’s trumpet (Brugmansia) poisoning: Clinical effects and epidemiology. Emerg. Med. 15, 376–382. doi: 10.1046/j.1442-2026.2003.00477.x

CrossRef Full Text | Google Scholar

ISIS (Instituto de Salud Incluyente) (2019). Reporte de coordinación en paralelo del Sistema de Monitoreo del Modelo Incluyente en Salud -SIMIS- (Guatemala: Reporte Interno ISIS).

Google Scholar

Jacobo-Herrera, N. J., Jacobo-Herrera, F. E., Zentella-Dehesa, A., Andrade-Cetto, A., Heinrich, M., Pérez-Plasencia, C. (2016). Medicinal plants used in Mexican traditional medicine for the treatment of colorectal cancer. J. Ethnopharmacol. 179, 391–402. doi: 10.1016/j.jep.2015.12.042

PubMed Abstract | CrossRef Full Text | Google Scholar

Jacobo-Salcedo, M. D. R., Alonso-Castro, A. J., Salazar-Olivo, L. A., Carranza-Alvarez, C., Gonzaĺez-Espińdola, L. A., Domińguez, F., et al. (2011). Antimicrobial and cytotoxic effects of Mexican medicinal plants. Nat. Prod. Commun. 6, 1925–1928. doi: 10.1177/1934578X1100601234

PubMed Abstract | CrossRef Full Text | Google Scholar

Jadhav, V. M., Thorat, R. M., Kadam, V. J., Sathe, N. S. (2009). Hibiscus rosa sinensis Linn. – “rudrapuspa”: a review. J. Pharm. Res. 2, 1168–1173.

Google Scholar

Jain, N. K., Kulkarni, S. K. (1999). Antinociceptive and anti-inflammatory effects of Tanacetum parthenium L. extract in mice and rats. J. Ethnopharmacol. 68, 251–259. doi: 10.1016/S0378-8741(99)00115-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Jain, R., Sharma, A., Gupta, S., Sarethy, I. P., Gabrani, R. (2011). Solanum nigrum: Current perspectives on therapeutic properties. Altern. Med. Rev. 16, 78–85.

PubMed Abstract | Google Scholar

Jamkhande, P. G., Wattamwar, A. S. (2015). Annona reticulata Linn. (Bullock’s heart): Plant profile, phytochemistry and pharmacological properties. J. Tradit. Complement. Med. 5, 144–152. doi: 10.1016/j.jtcme.2015.04.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Janwitthayanuchit, K., Kupradinun, P., Rungsipipat, A., Kettawan, A., Butryee, C. (2016). A 24-weeks toxicity study of Eryngium foetidum Linn. leaves in mice. Toxicol. Res. 32, 231–237. doi: 10.5487/TR.2016.32.3.231

PubMed Abstract | CrossRef Full Text | Google Scholar

Jaramillo-García, V., Trindade, C., Lima, E., Guecheva, T. N., Villela, I., Martinez-Lopez, W., et al. (2018). Chemical characterization and cytotoxic, genotoxic, and mutagenic properties of Baccharis trinervis (Lam, Persoon) from Colombia and Brazil. J. Ethnopharmacol. 213, 210–220. doi: 10.1016/j.jep.2017.10.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Jasso Díaz, G., Torres Hernández, G., Zamilpa, A., Becerril Pérez, C. M., Ramírez Bribiesca, J. E., et al. (2017). In vitro assessment of Argemone mexicana, Taraxacum officinale, Ruta chalepensis and Tagetes filifolia against Haemonchus contortus nematode eggs and infective (L3) larvae. Microb. Pathog. 109, 162–168. doi: 10.1016/j.micpath.2017.05.048

PubMed Abstract | CrossRef Full Text | Google Scholar

Jenett-Siems, K., Köhler, I., Kraft, C., Siems, K., Solis, P. N., Gupta, M. P., et al. (2003). Cornutins C–L, neo-clerodane-type diterpenoids from Cornutia grandifolia var. intermedia. Phytochemistry 64, 797–804. doi: 10.1016/S0031-9422(03)00352-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Jesus, D., Oliveira, J. R., Oliveira, F. E., Higa, K. C., Junqueira, J. C., Jorge, A. O. C., et al. (2015). Persea americana glycolic extract: In vitro study of antimicrobial activity against Candida albicans biofilm and cytotoxicity evaluation. Sci. World J. 2015, 531972. doi: 10.1155/2015/531972

CrossRef Full Text | Google Scholar

Jiménez-Arellanes, A., Luna-Herrera, J., Ruiz-Nicolás, R., Cornejo-Garrido, J., Tapia, A., Yépez-Mulia, L. (2013). Antiprotozoal and antimycobacterial activities of Persea americana seeds. BMC Complement. Altern. Med. 13, 109. doi: 10.1186/1472-6882-13-109

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiménez-Suárez, V., Nieto-Camacho, A., Jiménez-Estrada, M., Alvarado Sánche, B. (2016). Anti-inflammatory, free radical scavenging and alpha-glucosidase inhibitory activities of Hamelia patens and its chemical constituents. Pharm. Biol. 54, 1822–3180. doi: 10.3109/13880209.2015.1129544

PubMed Abstract | CrossRef Full Text | Google Scholar

Jin, M., Kijima, A., Suzuki, Y., Hibi, D., Inoue, T., Ishii, Y., et al. (2011). Comprehensive toxicity study of safrole using a medium-term animal model with gpt delta rats. Toxicology 290, 312–321. doi: 10.1016/j.tox.2011.09.088

PubMed Abstract | CrossRef Full Text | Google Scholar

Johnson, R. J., Wesseling, C., Newman, L. S. (2019). Chronic Kidney Disease of Unknown Cause in Agricultural Communities. N Engl. J. Med. 380, 1843–1852. doi: 10.1056/NEJMra1813869

PubMed Abstract | CrossRef Full Text | Google Scholar

Johnson, W. (2007). Final Report on the Safety Assessment of Capsicum annuum extract, Capsicum annuum fruit extract, Capsicum annuum resin, Capsicum annuum fruit powder, Capsicum frutescens fruit, Capsicum frutescens fruit extract, Capsicum frutescens resin, and capsaicin. Int. J. Toxicol. 26, 3–106. doi: 10.1080/10915810601163939

CrossRef Full Text | Google Scholar

Juárez-Vázquez, M., Carranza-Álvarez, C., Alonso-Castro, A. J., González-Alcaraz, V. F., Bravo-Acevedo, E., Chamarro-Tinajero, F. J., et al. (2013a). Ethnobotany of medicinal plants used in Xalpatlahuac, Guerrero, México. J. Ethnopharmacol. 148, 521–527. doi: 10.1016/j.jep.2013.04.048

PubMed Abstract | CrossRef Full Text | Google Scholar

Juárez-Vázquez, M., Josabad Alonso-Castro, A., García-Carrancá, A. (2013b). Kaempferitrin induces immunostimulatory effects in vitro. J. Ethnopharmacol. 148, 337–340. doi: 10.1016/j.jep.2013.03.072

PubMed Abstract | CrossRef Full Text | Google Scholar

Kacem, M., Kacem, I., Simon, G., Ben Mansour, A., Chaabouni, S., Elfeki, A., et al. (2015). Phytochemicals and biological activities of Ruta chalepensis L. growing in Tunisia. Food Biosci. 12, 73–83. doi: 10.1016/j.fbio.2015.08.001

CrossRef Full Text | Google Scholar

Kaewklom, S., Wongchai, M., Petvises, S., Hanpithakphong, W., Aunpad, R. (2018). Structural and biological features of a novel plant defensin from Brugmansia x candida. PloS One 13, e0201668. doi: 10.1371/journal.pone.0201668

PubMed Abstract | CrossRef Full Text | Google Scholar

Kalayou, S., Haileselassie, M., Gebre-egziabher, G., Tiku’e, T., Sahle, S., Taddele, H., et al. (2012). In vitro antimicrobial activity screening of some ethnoveterinary medicinal plants traditionally used against mastitis, wound and gastrointestinal tract complication in Tigray Region, Ethiopia. Asian Pac. J. Trop. Biomed. 2, 516–522. doi: 10.1016/S2221-1691(12)60088-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Kamatou, G. P., Vermaak, I., Viljoen, A. M. (2012). Eugenol—From the Remote Maluku Islands to the International Market Place: A Review of a Remarkable and Versatile Molecule. Molecules 17, 6953–6981. doi: 10.3390/molecules17066953

PubMed Abstract | CrossRef Full Text | Google Scholar

Karuppiah, P., Mustaffa, M. (2013). Antibacterial and antioxidant activities of Musa sp. leaf extracts against multidrug resistant clinical pathogens causing nosocomial infection. Asian Pac. J. Trop. Biomed. 3, 737–742. doi: 10.1016/S2221-1691(13)60148-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Keifer, D., Ulbricht, C., Abrams, T., Basch, E., Giese, N., Giles, M., et al. (2007). Peppermint (Mentha ×piperita): An evidence-based systematic review by the Natural Standard Research Collaboration. J. Herb. Pharmacother. 7, 91–143. doi: 10.1300/J157v07n02_07

PubMed Abstract | CrossRef Full Text | Google Scholar

Kermanshai, R., McCarry, B. E., Rosenfeld, J., Summers, P. S., Weretilnyk, E. A., Sorger, G. J. (2001). Benzyl isothiocyanate is the chief or sole anthelmintic in papaya seed extracts. Phytochemistry 57, 427–435. doi: 10.1016/S0031-9422(01)00077-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Kierans, C., Padilla-Altamira, C., Garcia-Garcia, G., Ibarra-Hernandez, M., Mercado, F. J. (2013). When health systems are barriers to health care: Challenges faced by uninsured Mexican kidney patients. PloS One 8 (1), e54380. doi: 10.1371/journal.pone.0054380

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, Y., Kim, J., Kim, O. J., Kim, W. C. (2014). Intoxication by angel’s trumpet: case report and literature review. BMC Res. Notes 7, 553. doi: 10.1186/1756-0500-7-553

PubMed Abstract | CrossRef Full Text | Google Scholar

Kirchhoff, P. (1943). Mesoamérica, sus límites geográficos, composición étnica y caracteres culturales. Acta Americana 1, 92–107.

Google Scholar

Kleinman, A., Benson, P. (2006). Anthropology in the clinic: The problem of cultural competency and how to fix it. PloS Med. 3, e294. doi: 10.1371/journal.pmed.0030294

PubMed Abstract | CrossRef Full Text | Google Scholar

Klimpel, S., Abdel-Ghaffar, F., Al-Rasheid, K. A. S., Aksu, G., Fischer, K., Strassen, B., et al. (2011). The effects of different plant extracts on nematodes. Parasitol Res. 108, 1047–1054. doi: 10.1007/s00436-010-2168-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Konaté, K., Bassolé, I. H. N., Hilou, A., Aworet-Samseny, R. R. R., Souza, A., Barro, N., et al. (2012). Toxicity assessment and analgesic activity investigation of aqueous acetone extracts of Sida acuta Burn f. and Sida cordifolia L. (Malvaceae), medicinal plants of Burkina Faso. BMC Complement. Altern. Med. 12, 120. doi: 10.1186/1472-6882-12-120

PubMed Abstract | CrossRef Full Text | Google Scholar

Kouitcheu-Mabeku, L. B., Eyoum Bille, B., Nguepi, E. (2016). In vitro and in vivo anti-Helicobacter activities of Eryngium foetidum (Apiaceae), Bidens pilosa (Asteraceae), and Galinsoga ciliata (Asteraceae) against Helicobacter pylori. BioMed. Res. Int. 2016, 2171032. doi: 10.1155/2016/2171032

PubMed Abstract | CrossRef Full Text | Google Scholar

Krenzelok, E. P. (2010). Aspects of Datura poisoning and treatment. Clin. Toxicol. 48, 104–110. doi: 10.3109/15563651003630672

CrossRef Full Text | Google Scholar

Kufer, J., Förther, H., Pöll, E., Heinrich, M. (2005). Historical and modern medicinal plant use – the example of the Ch’orti’ Maya and Ladinos in Eastern Guatemala. J. Pharm. Pharmacol. 57, 1127–1152. doi: 10.1211/jpp.57.9.0008

PubMed Abstract | CrossRef Full Text | Google Scholar

Kuigoua, G. M., Kouam, S. F., Ngadjui, B. T., Schulz, B. E., Green, I. R., Choudhary, M. I., et al. (2010). Minor secondary metabolic products from the stem bark of Plumeria rubra Linn. displaying antimicrobial activities. Planta Med. 76, 620–625. doi: 10.1055/s-0029-1240611

PubMed Abstract | CrossRef Full Text | Google Scholar

Kumar, S. A., Venkatarathanamma, V., Saibabu, N., Seetharam, K. (2015). Antipyretic activity of Annona plants leaves on brewer’s yeast induced febrile rats. Asian J. Pharm. Clin. Res. 8, 210–212.

Google Scholar

Ladas, E. J., Rivas, S., Ndao, D., Damoulakis, D., Bao, Y. Y., Cheng, B., et al. (2014). Use of traditional and complementary/alternative medicine (TCAM) in children with cancer in Guatemala. Pediatr. Blood Cancer 61, 687–692. doi: 10.1002/pbc.24791

PubMed Abstract | CrossRef Full Text | Google Scholar

Larbie, C., Owusu Nyarkoh, C., Owusu Adjei, C. (2019). Phytochemical and Safety Evaluation of Hydroethanolic Leaf Extract of Tecoma stans (L.) Juss. ex Kunth. Evid. Based Complement. Alternat. Med. 2019, 7417624. doi: 10.1155/2019/7417624 eCollection 2019.

PubMed Abstract | CrossRef Full Text | Google Scholar

Laribi, B., Kouki, K., M’Hamdi, M., Bettaieb, T. (2015). Coriander (Coriandrum sativum L.) and its bioactive constituents. Fitoterapia 103, 9–26. doi: 10.1016/j.fitote.2015.03.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Last, J., Spasoff, R. A., Harris, S. (2001). A Dictionary of Epidemiology. 4th ed (Oxford: Oxford University Press).

Google Scholar

Laurell, A. (2010). Revisando las políticas y discursos de salud en América Latina. Med. Soc 5, 79–88.

Google Scholar

Leal, C. M., Orózco, N., Rivera, J., Monterroso, L., Cáceres, A. (2014). In vitro activity against Helicobacter pylori by ethanol extracts from sixteen medicinal plants used for chronic gastrointestinal diseases in Guatemala. Acta Hortic. 1030, 93–102. doi: 10.17660/ActaHortic.2014.1030.11

CrossRef Full Text | Google Scholar

Leite, J., De Lourdes V. Seabra, M., Maluf, E., Assolant, K., Suchecki, D., et al. (1986). Pharmacology of lemongrass (Cymbopogon citratus (DC.) Stapf). III. Assessment of eventual toxic, hypnotic and anxiolytic effects on humans. J. Ethnopharmacol. 17, 75–83. doi: 10.1016/0378-8741(86)90074-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Lentz, D. L., Clark, A. M., Hufford, C. D., Meurer-Grimes, B., Passreiter, C. M., Cordero, J., et al. (1998). Antimicrobial properties of Honduran medicinal plants. J. Ethnopharmacol. 63, 253–263. doi: 10.1016/S0378-8741(98)00100-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Leonti, M., Vibrans, H., Sticher, O., Heinrich, M. (2001). Ethnopharmacology of the Popoluca, Mexico: an evaluation. J.Pharm. Pharmacol. 53, 1653–1669. doi: 10.1211/0022357011778052

PubMed Abstract | CrossRef Full Text | Google Scholar

Leonti, M., Sticher, O., Heinrich, M. (2003). Antiquity of medicinal plant usage in two Macro-Mayan ethnic groups (México). J. Ethnopharmacol. 88, 119–124. doi: 10.1016/S0378-8741(03)00188-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Leonti, M., Cabras, S., Castellanos, M. E., Challenger, A., Gertsch, J., Casu, L. (2013). Bioprospecting: Evolutionary implications from a post-olmec pharmacopoeia and the relevance of widespread taxa. J. Ethnopharmacol. 147, 92–107. doi: 10.1016/j.jep.2013.02.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Leonti, M. (2011). The future is written: Impact of scripts on the cognition, selection, knowledge and transmission of medicinal plant use and its implications for ethnobotany and ethnopharmacology. J. Ethnopharmacol. 134, 542–555. doi: 10.1016/j.jep.2011.01.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Levecke, B., Buttle, D. J., Behnke, J. M., Duce, I. R., Vercruysse, J. (2014). Cysteine proteinases from papaya (Carica papaya) in the treatment of experimental Trichuris suis infection in pigs: two randomized controlled trials. Parasitol. Vectors 7:255. doi: 10.1186/1756-3305-7-255

CrossRef Full Text | Google Scholar

Lima, E. B. C., Sousa, C. N. S., Meneses, L. N., Ximenes, N. C., Santos Júnior, M. A., Vasconcelos, G. S., et al. (2015). Cocos nucifera (L.) (Arecaceae): A phytochemical and pharmacological review. Braz. J. Med. Biol. Res. 48, 953–964. doi: 10.1590/1414-431X20154773

PubMed Abstract | CrossRef Full Text | Google Scholar

Linck, V. M., da Silva, A. L., Figueiró, M., Caramão, E. B., Moreno, P. R., Elisabetsky, E. (2010). Effects of Inhaled Linalool in Anxiety, Social Interaction and Aggressive Behavior in Mice. Phytomedicine 17, 679–683. doi: 10.1016/j.phymed.2009.10.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Loera, J. A., Reyes-Ortiz, C., Kuo, Y.-F. (2007). Predictors of complementary and alternative medicine use among older Mexican Americans. Complement. Ther. Clin. Pract. 13, 224–231. doi: 10.1016/j.ctcp.2007.03.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Lomash, V., Parihar, S. K., Jain, N. K., Katiyar, A. K. (2010). Effect of Solanum nigrum and Ricinus communis extracts on histamine and carrageenan-induced inflammation in the chicken skin. Cell. Mol. Biol. 56, OL1239–OL1251. doi: 10.1170/141

CrossRef Full Text | Google Scholar

López Barreiro, M., García Hernández, A. I., Rodríguez, E. B., Rodríguez, Z. M. (2014). Acute topical toxicity and dermal irritability of decoction of Piper auritum Kunth (Caisimón de anís). Rev. Cuba. Plantas Med. 19, 443–450.

Google Scholar

López de Guimaraes, D., Neyra Llanos, R. S., Romero Acevedo, J. H. (2001). Ascaridiasis: comparación de la eficacia terapeutica entre paico y albendazol en niños de Huaraz. Rev. Gastroenterol. Peru 21, 212–219.

PubMed Abstract | Google Scholar

López-Romero, J. C., González-Ríos, H., Peña-Ramos, A., Velazquez, C., Navarro, M., Robles-Zepeda, R., et al. (2018). Seasonal Effect on the Biological Activities of Litsea glaucescens Kunth Extracts. Evid. Based Complement. Alternat. Med. 2018, 2738489. doi: 10.1155/2018/2738489 eCollection 2018.

PubMed Abstract | CrossRef Full Text | Google Scholar

López-Rubalcava, C., Estrada-Camarena, E. (2016). Mexican medicinal plants with anxiolytic or antidepressant activity: Focus on preclinical research. J. Ethnopharmacol. 186, 377–391. doi: 10.1016/j.jep.2016.03.053

PubMed Abstract | CrossRef Full Text | Google Scholar

Lozoya, X., Zolla, C. (1984). Medicina tradicional en México. Bol. Oficina Sanit. Panam. 96, 360–364.

PubMed Abstract | Google Scholar

Lozoya, X., Reyes-Morales, H., Chávez-Soto, M. A., Martı́nez-Garcı́a, M.d. C., Soto-González, Y., Doubova, S. V. (2002). Intestinal anti-spasmodic effect of a phytodrug of Psidium guajava folia in the treatment of acute diarrheic disease. J. Ethnopharmacol. 83, 19–24. doi: 10.1016/S0378-8741(02)00185-X

PubMed Abstract | CrossRef Full Text | Google Scholar

Luoga, W., Mansur, F., Lowe, A., Duce, I. R., Buttle, D. J., Behnke, J. M. (2015). Factors affecting the anthelmintic efficacy of papaya latex in vivo: host sex and intensity of infection. Parasitol. Res. 114, 2535–2541. doi: 10.1007/s00436-015-4456-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Luz, D. A., Pinheiro, A. M., Silva, M. L., Monteiro, M. C., Prediger, R. D., Maia, C. S. F., et al. (2016). Ethnobotany, phytochemistry and neuropharmacological effects of Petiveria alliacea L. (Phytolaccaceae): A review. J. Ethnopharmacol. 185, 182–201. doi: 10.1016/j.jep.2016.02.053

PubMed Abstract | CrossRef Full Text | Google Scholar

MacDonald, D., VanCrey, K., Harrison, P., Rangachari, P. K., Rosenfeld, J., Warren, C., et al. (2004). Ascaridole-less infusions of Chenopodium ambrosioides contain a nematocide(s) that is(are) not toxic to mammalian smooth muscle. J. Ethnopharmacol. 92, 215–221. doi: 10.1016/j.jep.2004.02.018

PubMed Abstract | CrossRef Full Text | Google Scholar

MacKinnon, S., Durst, T., Arnason, J. T., Angerhofer, C., Pezzuto, J., Sanchez-Vindas, P. E., et al. (1997). Antimalarial activity of tropical Meliaceae extracts and gedunin derivatives. J. Nat. Prod. 60, 336–341. doi: 10.1021/np9605394

PubMed Abstract | CrossRef Full Text | Google Scholar

Magaña-Alejandro, M. A., Gama-Campillo, L. M., Mariaca-Méndez, R. (2010). El uso de las plantas medicinales en las comunidades Maya-Chontales de Nacajuca, Tabasco, México. Polibotánica 29, 213–262.

Google Scholar

Mahmoud-Awny, M., Attia, A. S., Abd-Ellah, M. F., El-Abhar, H. S. (2015). Mangiferin mitigates gastric ulcer in ischemia/reperfused rats: involvement of PPAR-γ, NF-κB and Nrf2/HO-1 signaling pathways. PloS One 10, e0132497. doi: 10.1371/journal.pone.0132497

PubMed Abstract | CrossRef Full Text | Google Scholar

Maldini, M., Sosa, S., Montoro, P., Giangaspero, A., Balick, M. J., Pizza, C., et al. (2009). Screening of the topical anti-inflammatory activity of the bark of Acacia cornigera Willdenow, Byrsonima crassifolia Kunth, Sweetia panamensis Yakovlev and the leaves of Sphagneticola trilobata Hitchcock. J. Ethnopharmacol. 122, 430–433. doi: 10.1016/j.jep.2009.02.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Mannelli, L. D.-C., Tenci, B., Zanardelli, M., Maidecchi, A., Lugli, A., Mattoli, L., et al. (2015). Widespread pain reliever profile of a flower extract of Tanacetum parthenium. Phytomedicine 22, 752–758. doi: 10.1016/j.phymed.2015.05.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Marroquin, E. A., Blanco, J. A., Granados, S., Cáceres, A., Morales, C. (1997). Clinical trial of Jatropha curcas sap in the treatment of common warts. Fitoterapia 68, 160–162.

Google Scholar

Martı́nez-Vázquez, M., González-Esquinca, A. R., Cazares Luna, L., Moreno Gutiérrez, M. N., Garcı́a-Argáez, A. N. (1999). Antimicrobial activity of Byrsonima crassifolia (L.) H.B.K. J. Ethnopharmacol. 66, 79–82. doi: 10.1016/S0378-8741(98)00155-X

PubMed Abstract | CrossRef Full Text | Google Scholar

Martínez, R., Diaz, B., Vásquez, L., Compagnone, R. S., Tillett, S., Canelón, D. J., et al. (2009). Chemical composition of essential oils and toxicological evaluation of Tagetes erecta and Tagetes patula from Venezuela. J. Essent. Oil Bear. Plants 12, 476–481. doi: 10.1080/0972060X.2009.10643747

CrossRef Full Text | Google Scholar

Martinez-Alfaro, M. A. (1984). Medicinal plants used in a Totonac community of the sierra norte de Puebla: tuzamapan de galeana, Puebla, Mexico. J. Ethnopharmacol. 11, 203–221. doi: 10.1016/0378-8741(84)90039-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Martínez-Toledo, V., Ordaz-Téllez, M. G., Castañeda-Sortribrán, A. N., Andrade-Cetto, A., Rodríguez-Arnaiz, R. (2008). Genotoxicity testing of Cecropia obtusifolia extracts in two in vivo assays: The wing somatic mutation and recombination test of Drosophila and the human cytokinesis-block micronucleus test. J. Ethnopharmacol. 116, 58–63. doi: 10.1016/j.jep.2007.10.041

PubMed Abstract | CrossRef Full Text | Google Scholar

Martins, D. T. O., Rodrigues, E., Casu, L., Benítez, G., Leonti, M. (2019). The historical development of pharmacopoeias and the inclusion of exotic herbal drugs with a focus on Europe and Brazil. J. Ethnopharmacol. 240:111891. doi: 10.1016/j.jep.2019.111891

PubMed Abstract | CrossRef Full Text | Google Scholar

Mathema, V. B., Koh, Y.-S., Thakuri, B. C., Sillanpää, M. (2012). Parthenolide, a sesquiterpene lactone, expresses multiple anti-cancer and anti-inflammatory activities. Inflammation 35, 560–565. doi: 10.1007/s10753-011-9346-0

PubMed Abstract | CrossRef Full Text | Google Scholar

McKay, D. L., Blumberg, J. B. (2006). A Review of the bioactivity and potential health benefits of chamomile tea (Matricaria recutita L.). Phytother. Res. 20, 519–530. doi: 10.1002/ptr.1900

PubMed Abstract | CrossRef Full Text | Google Scholar

McKinnon, R., Binder, M., Zupkó, I., Afonyushkin, T., Lajter, I., Vasas, A., et al. (2014). Pharmacological insight into the anti-inflammatory activity of sesquiterpene lactones from Neurolaena lobata (L.) R.Br. ex Cass. Phytomedicine 21, 1695–1701. doi: 10.1016/j.phymed.2014.07.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Medhi, B., Kishore, K., Singh, U., Seth, S. D. (2009). Comparative clinical trial of castor oil and diclofenac sodium in patients with osteoarthritis. Phyther. Res. 23, 1469–1473. doi: 10.1002/ptr.2804

CrossRef Full Text | Google Scholar

Mekhora, C., Muangnoi, C., Chingsuwanrote, P., Dawilai, S., Svasti, S., Chasri, K., et al. (2012). Eryngium foetidum suppresses inflammatory mediators produced by macrophages. Asian Pac. J. Cancer Prev. 13, 653–664. doi: 10.7314/apjcp.2012.13.2.653

PubMed Abstract | CrossRef Full Text | Google Scholar

Meléndez, P. A., Capriles, V. A. (2006). Antibacterial properties of tropical plants from Puerto Rico. Phytomedicine 13, 272–276. doi: 10.1016/j.phymed.2004.11.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Messer, E. (1975). Zapotec plant knowledge: classification, uses, and communication about plants in Mitla (Oaxaca, Mexico. [PhD thesis]. [Ann Arbor (MI)]: University of Michigan).

Google Scholar

Michel, J., Duarte, R. E., Bolton, J. L., Huang, Y., Cáceres, A., Veliz, M., et al. (2007). Medical potential of plants used by the Q’eqchi Maya of Livingston, Guatemala for the treatment of women’s health complaints. J. Ethnopharmacol. 114, 92–101. doi: 10.1016/j.jep.2007.07.033

PubMed Abstract | CrossRef Full Text | Google Scholar

Michel, J. L., Cáceres, A., Mahady, G. B. (2016). Ethnomedical research and review of Q’eqchi Maya women’s reproductive health in the Lake Izabal region of Guatemala: past, present and future prospects. J. Ethnopharmacol. 178, 307–322. doi: 10.1016/j.jep.2015.12.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Michelin, D. C., de Almeida, G. C., Galina, K. J., Lopes, G. C., Nakamura, C. V., Dias Filho, B. P., et al. (2010). Antidiarrheal activity of Guazuma ulmifolia Lam. (Sterculiaceae). Lat. Am. J. Pharm. 29, 1024–1028.

Google Scholar

Michl, J., Ingrouille, M. J., Simmonds, M. S., Heinrich, M. (2014). Naturally occurring aristolochic acid analogues and their toxicities. Nat. Prod. Rep. 31, 676–693. doi: 10.1039/c3np70114j

PubMed Abstract | CrossRef Full Text | Google Scholar

Miller, A. B., Cates, R. G., Lawrence, M., Soria, J. A. F., Espinoza, L. V., Martinez, J. V., et al. (2015). The antibacterial and antifungal activity of essential oils extracted from Guatemalan medicinal plants. Pharm. Biol. 53, 548–554. doi: 10.3109/13880209.2014.932391

PubMed Abstract | CrossRef Full Text | Google Scholar

Miranda-Cruz, E., Espinosa-Moreno, J., Centurión-Hidalgo, D., Velázquez-Martínez, J. R., Alor-Chávez, M. J. (2012). Antimicrobial activity of Psidium friedrichsthalianum L., Pterocarpus hayesii L., Tynanthus guatemalensis L. and Spondias purpurea L. extracts. Bol. Latinoam. Caribe Plantas Med. Aromat. 11, 354–361.

Google Scholar

Mitznegg, P., Hach, B., Heim, F. (1970). The influence of caffeine on endogenous cyclic 3’,5’ -AMP and uterine smooth muscle contraction induced by oxytocin. Life Sci. I. 9, 975–981. doi: 10.1016/0024-3205(70)90120-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Moerman, D. E., Jonas, W. B. (2002). Deconstructing the placebo effect and finding the meaning response. Ann. Intern. Med. 136, 471–476. . doi: 10.7326/0003-4819-136-6-200203190-00011

PubMed Abstract | CrossRef Full Text | Google Scholar

Mohsenzadeh, F., Chehregani, A., Amiri, H. (2011). Chemical composition, antibacterial activity and cytotoxicity of essential oils of Tanacetum parthenium in different developmental stages. Pharm. Biol. 49, 920–926. doi: 10.3109/13880209.2011.556650

PubMed Abstract | CrossRef Full Text | Google Scholar

Mokdad, A. H., Colson, K. E., Zúñiga-Brenes, P., Ríos-Zertuche, D., Palmisano, E. B., Alfaro-Porras, E., et al. (2015). Salud Mesoamérica 2015 Initiative: design, implementation, and baseline findings. Popul. Health Metr. 13, 3. doi: 10.1186/s12963-015-0034-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Monzote, L., García, M., Montalvo, A. M., Scull, R., Miranda, M. (2010). Chemistry, cytotoxicity and antileishmanial activity of the essential oil from Piper auritum. Mem. Inst. Oswaldo Cruz. 105, 2. doi: 10.1590/S0074-02762010000200010

CrossRef Full Text | Google Scholar

Monzote, L., Pastor, J., Scull, R., Gille, L. (2014). Antileishmanial activity of essential oil from Chenopodium ambrosioides and its main components against experimental cutaneous leishmaniasis in BALB/c mice. Phytomedicine 21, 1048–1052. doi: 10.1016/j.phymed.2014.03.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Morais-Braga, M. F. B., Carneiro, J. N. P., Machado, A. J. T., dos Santos, A. T. L., Sales, D. L., Lima, L. F., et al. (2016). Psidium guajava L., from ethnobiology to scientific evaluation: Elucidating bioactivity against pathogenic microorganisms. J. Ethnopharmacol. 194, 1140–1152. doi: 10.1016/j.jep.2016.11.017

PubMed Abstract | CrossRef Full Text | Google Scholar

MSPAS (Ministerio de Salud Pública y Asistencia Social) (2018). Normas de Atención en Salud Integral para el Primer y Segundo Nivel (Guatemala: Gobierno de Guatemala). Available at: https://www.mspas.gob.gt/index.php/component/jdownloads/send/251-normas-de-atencion/2060-normas-de-atencion-en-salud-integral-2018 (Accessed on January 5th, 2020).

Google Scholar

Mullally, M., Cayer, C., Muhammad, A., Walshe-Roussel, B., Ahmed, F., Sanchez-Vindas, P. E., et al. (2016). Anxiolytic activity and active principles of Piper amalago (Piperaceae), a medicinal plant used by the Q’eqchi’ Maya to treat susto, a culture-bound illness. J. Ethnopharmacol. 185, 147–154 . doi: 10.1016/j.jep.2016.03.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Mumtaz, S. M. F., Paul, S., Bag, A. K. (2013). Effect of Sechium edule on chemical induced kidney damage in experimental animals. Bangladesh J. Pharmacol. 8, 28–35. doi: 10.3329/bjp.v8i1.12982

CrossRef Full Text | Google Scholar

Murthy, K. N. C., Reddy, K. V., Veigas, J. M., Murthy, U. D. (2004). Study on wound healing activity of Punica granatum peel. J. Med. Food 7, 256–259. doi: 10.1089/1096620041224111

PubMed Abstract | CrossRef Full Text | Google Scholar

Mwangi, G. G., Wagacha, J. M., Nguta, J. M., Mbaria, J. M. (2015). Brine shrimp cytotoxicity and antimalarial activity of plants traditionally used in treatment of malaria in Msambweni district. Pharm. Biol. 53, 588–593. doi: 10.3109/13880209.2014.935861

PubMed Abstract | CrossRef Full Text | Google Scholar

Myers, N., Mittermeier, R. A., Mittermeier, C. G., da Fonseca, G. A., Kent, J. (2000). Biodiversity hotspots for conservation priorities. Nature 403, 853–858. doi: 10.1038/35002501

PubMed Abstract | CrossRef Full Text | Google Scholar

Nair, R., Chanda, S. (2008). Antimicrobial activity of Terminalia catappa, Manilkara zapota and Piper betel leaf extract. Indian J. Pharm. Sci. 70, 390–393. doi: 10.4103/0250-474X.43012

PubMed Abstract | CrossRef Full Text | Google Scholar

Navarro, M. C., Montilla, M. P., Cabo, M. M., Galisteo, M., Cáceres, A., Morales, C., et al. (2003). Antibacterial, antiprotozoal and antioxidant activity of five plants used in Izabal for infectious diseases. Phyther. Res. 17, 325–329. doi: 10.1002/ptr.1134

CrossRef Full Text | Google Scholar

Nayak, B. S., Raju, S. S., Chalapathi Rao, A. V. (2008). Wound healing activity of Persea americana (avocado) fruit: a preclinical study on rats. J. Wound Care 17, 123–125. doi: 10.12968/jowc.2008.17.3.28670

PubMed Abstract | CrossRef Full Text | Google Scholar

Nayak, B. S., Marshall, M. R., Isitor, G. (2010). Wound healing potential of ethanolic extract of Kalanchoe pinnata lam. leaf-a preliminary study. Indian J. Exp. Biol. 48, 572–576.

PubMed Abstract | Google Scholar

Nayak, B. S., Ramlogan, S., Chalapathi Rao, A., Maharaj, S. (2014). Neurolaena lobata L. promotes wound healing in Sprague Dawley rats. Int. J. Appl. Basic Med. Res. 4, 106–110. doi: 10.4103/2229-516X.136791

PubMed Abstract | CrossRef Full Text | Google Scholar

Nellis, D. N. (1997). Poisonous Plants and Animals of Florida and the Caribbean (Sarasota: Pineapple Press).

Google Scholar

Nicolas, J. P. (1997). Pharmacopée traditionelle de Maya K’iché: etude ethnopharmacologique et système de classification indigène (Lille: PhD dissertation at the University of Lille).

Google Scholar

Nicolas, J. P. (1999). Plantes médicinales des Mayas K’iché du Guatemala (Paris: Ibis Press).

Google Scholar

Nigenda, G., Mora-Flores, G., Aldama-López, S., Orozco-Núñez, E. (2001). The practice of traditional medicine in Latin America and the Caribbean: the dilemma between regulation and tolerance. Salud Publica Mex. 43, 41–51. doi: 10.1590/S0036-36342001000100006

PubMed Abstract | CrossRef Full Text | Google Scholar

Nikkhah-Bodagh, M., Maleki, I., Hekmatdoost, A. (2019). Ginger in gastrointestinal disorders: A systematic review of clinical trials. Food Sci. Nutr. 7, 96–108. doi: 10.1002/fsn3.807

PubMed Abstract | CrossRef Full Text | Google Scholar

Nneli, R. O., Woyike, O. A. (2008). Antiulcerogenic effects of coconut (Cocos nucifera) extract in rats. Phyther. Res. 22, 970–972. doi: 10.1002/ptr.2318

CrossRef Full Text | Google Scholar

Oliveira, L. M. B., Bevilaqua, C. M. L., Costa, C. T. C., Macedo, I. T. F., Barros, R. S., Rodrigues, A. C. M., et al. (2009). Anthelmintic activity of Cocos nucifera L. against sheep gastrointestinal nematodes. Vet. Parasitol. 159, 55–59. doi: 10.1016/j.vetpar.2008.10.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Ooi, C. P., Yassin, Z., Hamid, T.-A. (2012). Momordica charantia for type 2 diabetes mellitus. Cochrane Database Syst. Rev. 8:CD007845. doi: 10.1002/14651858.CD007845.pub3

CrossRef Full Text | Google Scholar

Ordoñez, A. A. L., Gomez, J. D., Cudmani, N. M., Vattuone, M. A., Isla, M. I. (2003). Antimicrobial activity of nine extracts of Sechium edule (Jacq.) Swartz. Microb. Ecol. Health D. 15, 33–39. doi: 10.1080/0891060010015583

CrossRef Full Text | Google Scholar

Ordoñez, A. A. L., Ordoñez, R. M., Zampini, I. C., Isla, M. I. (2009). Design and quality control of a pharmaceutical formulation containing natural products with antibacterial, antifungal and antioxidant properties. Int. J. Pharmaceut. 378, 51–58. doi: 10.1016/j.ijpharm.2009.05.040

CrossRef Full Text | Google Scholar

Ortiz de Montellano, B. (1975). Empirical Aztec medicine. Science 188, 215–220. doi: 10.1126/science.1090996

PubMed Abstract | CrossRef Full Text | Google Scholar

Ortiz de Montellano, B. (1990). Aztec medicine, health, and nutrition (New Brunswick: Rutgers University Press).

Google Scholar

Oskay, M., Oskay, D., Kalnyoncu, F. (2009). Activity of some plant extracts against multi-drug resistant human pathogens. Iranian J. Pharm. Res. 8, 393–300. doi: 10.22037/IJPR.2010.825

CrossRef Full Text | Google Scholar

Owoyele, V. B., Wuraola, C. O., Soladoye, A. O., Olaleye, S. B. (2004). Studies on the anti-inflammatory and analgesic properties of Tithonia diversifolia leaf extract. J. Ethnopharmacol. 90, 317–321. doi: 10.1016/j.jep.2003.10.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Ozolua, R. I., Anaka, O. N., Okpo, S. O., Idogun, S. E. (2009). Acute and sub-acute toxicological assessment of the aqueous seed extract of Persea americana Mill (Lauraceae) in rats. Afr. J. Tradit. Complement. Altern. Med. 6, 573–578. doi: 10.4314/ajtcam.v6i4.57214

PubMed Abstract | CrossRef Full Text | Google Scholar

PAHO (2009). Health systems profile Belize: Monitoring and analyzing health systems change/reform (Washington D.C.: Pan American Health Organization).

Google Scholar

Panda, S. K., Mohanta, Y. K., Padhi, L., Park, Y.-H., Mohanta, T. K., Bae, H. (2016). Large scale screening of ethnomedicinal plants for identification of potential antibacterial compounds. Molecules 21, 293. doi: 10.3390/molecules21030293

PubMed Abstract | CrossRef Full Text | Google Scholar

Parvez, M. (2016). Pharmacological activities of Mango (Mangifera indica): A review. J. Pharmacogn. Phytochem. 5, 1–7.

Google Scholar

Parvin, M. S., Das, N., Jahan, N., Akhter, M. A., Nahar, L., Islam, M. E. (2015). Evaluation of in vitro anti-inflammatory and antibacterial potential of Crescentia cujete leaves and stem bark. BMC Res. Notes 8, 412. doi: 10.1186/s13104-015-1384-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Passoni, F. D., Oliveira, R. B., Chagas-Paula, D. A., Gobbo-Neto, L., Da Costa, F. B. (2013). Repeated-dose toxicological studies of Tithonia diversifolia (Hemsl.) A. gray and identification of the toxic compounds. J. Ethnopharmacol. 147, 389–394. doi: 10.1016/j.jep.2013.03.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Patel, S. (2011). Harmful and beneficial aspects of Parthenium hysterophorus: an update. 3 Biotech. 1, 1–9. doi: 10.1007/s13205-011-0007-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Pathan, R. K., Gali, P. R., Pathan, P., Gowtham, T., Pasupuleti, S. (2012). In vitro antimicrobial activity of Citrus aurantifolia and its phytochemical screening. Asian Pacific J. Trop. Dis. 2, S328–S331. doi: 10.1016/S2222-1808(12)60176-5

CrossRef Full Text | Google Scholar

Patro, G., Kumar Bhattamisra, S., Kumar Mohanty, B. (2016). Effects of Mimosa pudica L. leaves extract on anxiety, depression and memory. Avicenna J. Phytomed. 6, 696–710.

PubMed Abstract | Google Scholar

Paul, J. H. A., Seaforth, C. E. (2011). Harmful plants in Caribbean folk medicine. Focus Alt. Compl. Ther. 16, 261–265. doi: 10.1111/j.2042-7166.2011.01123.x

CrossRef Full Text | Google Scholar

Paul, J. H. A., Seaforth, C. E., Tikasingh, T. (2011). Eryngium foetidum L.: A review. Fitoterapia 82, 302–308. doi: 10.1016/j.fitote.2010.11.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Pavia, C. S., Pierre, A., Nowakowski, J. (2000). Antimicrobial activity of nicotine against a spectrum of bacterial and fungal pathogens. J. Med. Microbiol. 49, 675–676. doi: 10.1099/0022-1317-49-7-675

PubMed Abstract | CrossRef Full Text | Google Scholar

Peraza-Sánchez, S. R., Cen-Pacheco, F., Noh-Chimal, A., May-Pat, F., Simá-Polanco, P., Dumonteil, E., et al. (2007). Leishmanicidal evaluation of extracts from native plants of the Yucatan peninsula. Fitoterapia 78, 315–318. doi: 10.1016/j.fitote.2007.03.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Pereira, W. S., Ribeiro, B. P., Sousa, A. I. P., Serra, I. C. P. B., Mattar, N. S., Fortes, T. S., et al. (2010). Evaluation of the subchronic toxicity of oral treatment with Chenopodium ambrosioides in mice. J. Ethnopharmacol. 127, 602–605. doi: 10.1016/j.jep.2009.12.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Pérez, S., Meckes, M., Pérez, C., Susunaga, A., Zavala, M. A. (2005). Anti-inflammatory activity of Lippia dulcis. J. Ethnopharmacol. 102, 1–4. doi: 10.1016/j.jep.2005.06.047

PubMed Abstract | CrossRef Full Text | Google Scholar

Pérez Gutiérrez, R. M., Muñiz Ramirez, A. (2013). Hexane extract of the seeds of Byrsonima crassifolia accelerates wound healing in streptozotocin-induced diabetic rats. Chin. J. Integr. Med. 1–7. doi: 10.1007/s11655-013-1556-x

CrossRef Full Text | Google Scholar

Pérez-Guerrero, C., Herrera, M. D., Ortiz, R., Alvarez de Sotomayor, M., Fernández, M. A. (2001). A pharmacological study of Cecropia obtusifolia Bertol aqueous extract. J. Ethnopharmacol. 76, 279–284. doi: 10.1016/S0378-8741(01)00253-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Pérez-Ortega, G., González-Trujano, M. E., Ángeles-López, G. E., Brindis, F., Vibrans, H., Reyes-Chilpa, R. (2016). Tagetes lucida Cav.: Ethnobotany, phytochemistry and pharmacology of its tranquilizing properties. J. Ethnopharmacol. 181, 221–228. doi: 10.1016/j.jep.2016.01.040

PubMed Abstract | CrossRef Full Text | Google Scholar

Perry, N., Perry, E. (2006). Aromatherapy in the management of psychiatric disorders: clinical and neuropharmacological perspectives. CNS Drugs 20, 257–280. doi: 10.2165/00023210-200620040-00001

PubMed Abstract | CrossRef Full Text | Google Scholar

Peter, E. L., Kasali, F. M., Deyno, S., Mtewa, A., Nagendrappa, P. B., Tolo, C. U., et al (2019). Momordica charantia L. lowers elevated glycaemia in type 2 diabetes mellitus patients: Systematic review and meta-analysis. J. Ethnopharmacol. 231, 311–324. doi: 10.1016/j.jep.2018.10.033

PubMed Abstract | CrossRef Full Text | Google Scholar

Picking, D., Delgoda, R., Boulogne, I., Mitchell, S. (2013). Hyptis verticillata Jacq: A review of its traditional uses, phytochemistry, pharmacology and toxicology. J. Ethnopharmacol. 147, 16–41. doi: 10.1016/j.jep.2013.01.039

PubMed Abstract | CrossRef Full Text | Google Scholar

Pimenta, F. C. F., Alves, M. F., Pimenta, M. B. F., Melo, S. A. L., Almeida, A. A. F., Leite, J. R., et al. (2016). Anxiolytic effect of Citrus aurantium L. on patients with chronic myeloid leukemia. Phyther. Res. 30, 613–617. doi: 10.1002/ptr.5566

CrossRef Full Text | Google Scholar

Pittler, M. H., Ernst, E. (2004). Feverfew for preventing migraine. Cochrane Database Syst. Rev. 3, CD002286. doi: 10.1002/14651858.CD002286.pub3

CrossRef Full Text | Google Scholar

Puig, A., Pagán, J. A., Wong, R. (2009). Assessing quality across health care subsystems in Mexico. J. Ambul. Care Manage. 32, 123–131. doi: 10.1097/JAC.0b013e31819942e5

PubMed Abstract | CrossRef Full Text | Google Scholar

Qnais, E. Y., Elokda, A. S., Abu Ghalyun, Y. Y., Abdulla, F. A. (2007). Antidiarrheal activity of the aqueous extract of Punica granatum. (Pomegranate) Peels. Pharm. Biol. 45, 715–720. doi: 10.1080/13880200701575304

CrossRef Full Text | Google Scholar

Rahalison, L., Hamburger, M., Hostettmann, K., Monod, M., Frenk, E., Gupta, M. P., et al. (1993). Screening for Antifungal Activity of Panamanian Plants. Int. J. Pharmacogn. 31, 68–76. doi: 10.3109/13880209309082921

CrossRef Full Text | Google Scholar

Rahman, S., Parvez, A. K., Islam, R., Khan, M. H. (2011). Antibacterial activity of natural spices on multiple drug resistant Escherichia coli isolated from drinking water, Bangladesh. Ann. Clin. Microbiol. Antimicrob. 10:10. doi: 10.1186/1476-0711-10-10

PubMed Abstract | CrossRef Full Text | Google Scholar

Ramakrishna, B. S., Subramanian, V., Mohan, V., Sebastian, B. K., Young, G. P., Farthing, M. J., et al. (2008). A randomized controlled trial of glucose versus amylase resistant tarch hypo-osmolar oral rehydration solution for adult acute dehydrating diarrhea. PloS One 3, e1587. doi: 10.1371/journal.pone.0001587

PubMed Abstract | CrossRef Full Text | Google Scholar

Ramos, A., Rivero, R., Victoria, M. C., Visozo, A., Piloto, J. (2001). Assessment of mutagenicity in Parthenium hysterophorus L. J. Ethnopharmacol. 77, 25–30. doi: 10.1016/S0378-8741(01)00257-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Ramos, A., Rivero, R., Visozo, A., Piloto, J. (2002). Parthenin, a sesquiterpene lactone of Parthenium hysterophorus L. is a high toxicity clastogen. Mutat. Res. Toxicol. Environ. Mutagen. 514, 19–27. doi: 10.1016/S1383-5718(01)00321-7

CrossRef Full Text | Google Scholar

Ranasinghe, P., Pigera, S., Premakumara, G. A. S., Galappaththy, P., Constantine, G. R., Katulanda, P. (2013). Medicinal properties of “true” cinnamon (Cinnamomum zeylanicum): a systematic review. BMC Complement. Altern. Med. 13, 275. doi: 10.1186/1472-6882-13-275

PubMed Abstract | CrossRef Full Text | Google Scholar

Ranere, A. J., Piperno, D. R., Holst, I., Dickau, R., Iriarte, J. (2009). The cultural and chronological context of early Holocene maize and squash domestication in the Central Balsas River Valley, Mexico. Proc. Natl. Acad. Sci. 106, 5014–5018. doi: 10.1073/pnas.0812590106

CrossRef Full Text | Google Scholar

Rao, H. J., Lakshmi (2012). Antidiarrhoeal activity of the aqueous extract of the bark of Cinnamomum zeylanicum Linn in mice. J. Clin. Diagn. Res. 6, 215–219.

Google Scholar

Rasekh, H. R., Hosseinzadeh, L., Mehri, S., Kamli-Nejad, M., Aslani, M., Tanbakoosazan, F. (2012). Safety assessment of Ocimum basilicum hydroalcoholic extract in Wistar rats: Acute and subchronic toxicity Studies. Iran. J. Basic Med. Sci. 15, 645–653.

PubMed Abstract | Google Scholar

Rashidian, A., Roohi, P., Mehrzadi, S., Ghannadi, A. R., Minaiyan, M. (2015). Protective effect of Ocimum basilicum essential oil against acetic acid–induced colitis in rats. J. Evid. Based Integr. Med. 21, NP36–NP42. doi: 10.1177/2156587215616550

CrossRef Full Text | Google Scholar

Raymond Chia, T. W., Dykes, G. A. (2010). Antimicrobial activity of crude epicarp and seed extracts from mature avocado fruit (Persea americana) of three cultivars. Pharm. Biol. 48, 753–756. doi: 10.3109/13880200903273922

PubMed Abstract | CrossRef Full Text | Google Scholar

Rejón-Orantes, J. C., Suaréz, D. P. P., Rejón-Rodríguez, A., Hernández, S. H., Liévano, O. E. G., Rodríguez, D. L., et al. (2013). Aqueous root extracts from Mimosa albida Humb. & Bonpl. ex Willd. display antinociceptive activity in mice. J. Ethnopharmacol. 149, 522–526. doi: 10.1016/j.jep.2013.07.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Revilla-Monsalve, M. C., Andrade-Cetto, A., Palomino-Garibay, M. A., Wiedenfeld, H., Islas-Andrade, S. (2007). Hypoglycemic effect of Cecropia obtusifolia Bertol. aqueous extracts on type 2 diabetic patients. J. Ethnopharmacol. 111, 636–640. doi: 10.1016/j.jep.2007.01.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocha-Buelvas, A. (2017). Pueblos indígenas y salud colectiva: hacia una ecología de saberes (Physis: Revista de Saúde Coletiva). [Accesed May, 20, 2020].

Google Scholar

Rodríguez-García, C. M., Ruiz-Ruiz, J. C., Peraza-Echeverría, L., Peraza-Sánchez, S. R., Torres-Tapia, L. W., Pérez-Brito, D., et al. (2019). Antioxidant, antihypertensive, anti-hyperglycemic, and antimicrobial activity of aqueous extracts from twelve native plants of the Yucatan coast. PloS One 14, e0213493. doi: 10.1371/journal.pone.0213493

PubMed Abstract | CrossRef Full Text | Google Scholar

Román-Ramos, R., Flores-Saenz, J. L., Partida-Hernández, G., Lara-Lemus, A., Alarcón-Aguilar, F. (1991). Experimental study of the hypoglycemic effect of some antidiabetic plants. Arch. Invest. Méd. (Méx) 22, 87–93.

PubMed Abstract | Google Scholar

Romero-Cerecero, O., Tortoriello-García, J. (2007). Conocimiento sobre fitomedicamentos entre medicos del Segundo nivel de atención. Rev. Med. Inst. Mex. Seguro Soc 45, 453–458.

PubMed Abstract | Google Scholar

Rosas-Piñón, Y., Mejía, A., Díaz-Ruiz, G., Aguilar, M. I., Sánchez-Nieto, S., Rivero-Cruz, J. F. (2012). Ethnobotanical survey and antibacterial activity of plants used in the Altiplane region of Mexico for the treatment of oral cavity infections. J. Ethnopharmacol. 141, 860–865. doi: 10.1016/j.jep.2012.03.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Rubio-Piña, J., Vázquez-Flota, F. (2013). Pharmaceutical applications of the benzylisoquinoline alkaloids from Argemone mexicana L. Curr. Top. Med. Chem. 3, 2200–2207. doi: 10.2174/15680266113139990152

CrossRef Full Text | Google Scholar

Rukmini, J. N., Manasa, S., Rohini, C., Sireesha, L. P., Ritu, S., Umashankar, G. K. (2017). Antibacterial efficacy of tender coconut water (Cocos nucifera L.) on Streptococcus mutans: an in-vitro study. J. Int. Soc Prev. Community Dent. 7, 130–134. doi: 10.4103/jispcd.JISPCD_275_16

PubMed Abstract | CrossRef Full Text | Google Scholar

Saftlas, A. F., Triche, E. W., Beydoun, H., Bracken, M. B. (2010). Does chocolate intake during pregnancy reduce the risks of preeclampsia and gestational hypertension? Ann. Epidemiol. 20, 584–591. doi: 10.1016/j.annepidem.2010.05.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Sagar, L., Sehgal, R., Ojha, S. (2005). Evaluation of antimotility effect of Lantana camara L. var. acuelata constituents on neostigmine induced gastrointestinal transit in mice. BMC Complement. Altern. Med. 5:18. doi: 10.1186/1472-6882-5-18

PubMed Abstract | CrossRef Full Text | Google Scholar

Said Fernández, S., Ramos Guerra, M. C., Mata Cárdenas, B. D., Vargas Villarreal, J., Villarreal Treviño, L. (2005). In vitro antiprotozoal activity of the leaves of Artemisia ludoviciana. Fitoterapia 76, 466–468. doi: 10.1016/j.fitote.2005.04.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Sanati, S., Razavi, B. M., Hosseinzadeh, H. (2018). A review of the effects of Capsicum annuum L. and its constituent, capsaicin, in metabolic syndrome. Iran. J. Basic Med. Sci. 21, 439–448. doi: 10.22038/ijbms.2018.25200.6238

PubMed Abstract | CrossRef Full Text | Google Scholar

Sánchez-Mendoza, M. E., Reyes-Ramírez, A., Cruz Antonio, L., Martínez Jiménez, L., Rodríguez-Silverio, J., Arrieta, J. (2011). Bioassay-guided isolation of an anti-ulcer compound, Tagitinin C, from Tithonia diversifolia: role of nitric oxide, prostaglandins and sulfhydryls. Molecules 16, 665–674. doi: 10.3390/molecules16010665

PubMed Abstract | CrossRef Full Text | Google Scholar

Sandoval-Montemayor, N. E., García, A., Elizondo-Treviño, E., Garza-González, E., Alvarez, L., del Rayo Camacho-Corona, M. (2012). Chemical composition of hexane extract of Citrus aurantifolia and anti-Mycobacterium tuberculosis activity of some of its constituents. Molecules 17, 11173–11184. doi: 10.3390/molecules170911173

PubMed Abstract | CrossRef Full Text | Google Scholar

Sarris, J., McIntyre, E., Camfield, D. A. (2013). Plant-based medicines for anxiety disorders, part 2: a review of clinical studies with supporting preclinical evidence. CNS Drugs 27, 301–319. doi: 10.1007/s40263-013-0059-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Schep, L. J., Slaughter, R. J., Beasley, D. M. (2009). Nicotinic plant poisoning. Clin. Toxicol. 47, 771–781. doi: 10.1080/15563650903252186

CrossRef Full Text | Google Scholar

Schulz, V., Hänsel, R., Tyler, V. E. (2012). Rational phytotherapy: a physicians" guide to herbal medicine. 4th edition (Berlin: Springer Verlag).

Google Scholar

Semwal, D. K., Semwal, R. B., Vermaak, I., Viljoen, A. (2014). From arrow poison to herbal medicine – The ethnobotanical, phytochemical and pharmacological significance of Cissampelos (Menispermaceae). J. Ethnopharmacol. 155, 1011–1028. doi: 10.1016/j.jep.2014.06.054

PubMed Abstract | CrossRef Full Text | Google Scholar

Sepúlveda-Arias, J. C., Veloza, L. A., Escobar, L. M., Orozco, L. M., Lopera, I. A. (2013). Anti-inflammatory effects of the main constituents and epoxides derived from the essential oils obtained from Tagetes lucida, Cymbopogon citratus, Lippia alba and Eucalyptus citriodora. J. Essent. Oil Res. 25, 186–193. doi: 10.1080/10412905.2012.751556

CrossRef Full Text | Google Scholar

Shah, K. A., Patel, M. B., Patel, R. J., Parmar, P. K. (2010). Mangifera indica (Mango). Pharmacogn. Rev. 4, 42–48. doi: 10.4103/0973-7847.65325

PubMed Abstract | CrossRef Full Text | Google Scholar

Shaival, K. R., Iyengar, M. A., Girija, R. (2001). Anti-microbial activity of the essential oil of the leaves of Pimenta dioica Linn. (Family: Myrtaceae). Indian Drugs 38, 458–461.

Google Scholar

Sharifi-Rad, M., Mnayer, D., Tabanelli, G., Stojanovic-Radic, Z. Z., Sharifi-Rad, M., Yousaf, Z., et al. (2016). Plants of the genus Allium as antibacterial agents: From tradition to pharmacy. Cell. Mol. Biol. 62, 57–68. doi: 10.14715/cmb/2016.62.9.10

CrossRef Full Text | Google Scholar

Sharma, V. K., Sethuraman, G. (2007). Parthenium Dermatitis. Dermatitis 18, 183–190. doi: 10.2310/6620.2007.06003

PubMed Abstract | CrossRef Full Text | Google Scholar

Sharma, O. P., Sharma, S., Pattabhi, V., Mahato, S. B., Sharma, P. D. (2007). A Review of the Hepatotoxic Plant Lantana camara. Crit. Rev. Toxicol. 37, 313–352. doi: 10.1080/10408440601177863

PubMed Abstract | CrossRef Full Text | Google Scholar

Shashikumara, S., Prathima, C., Amrutheswari, B. (2018). Effect of ethanolic extract of Mimosa pudica root L. on acute restraint stress-induced anxiety and depression in Swiss albino mice. Asian J. Pharm. Clin. Res. 11, 182–186. doi: 10.22159/ajpcr.2018.v11i10.27180

CrossRef Full Text | Google Scholar

Shivaprasad, H. V., Rajesh, R., Nanda, B. L., Dharmappa, K. K., Vishwanath, B. S. (2009). Thrombin like activity of Asclepias curassavica L. latex: action of cysteine proteases. J. Ethnopharmacol. 123, 106–109. doi: 10.1016/j.jep.2009.02.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Shukla, P., Kumar, S. (2015). Acute toxicity study of ethanolic extract of Solanum lycopersicum (leaf) in Swiss albino mice. Int. J. Pharm. Sci. Res. 6, 361–366. doi: 10.13040/IJPSR.0975-8232.6

CrossRef Full Text | Google Scholar

Sidgwick, G. P., McGeorge, D., Bayat, A. (2015). A comprehensive evidence-based review on the role of topicals and dressings in the management of skin scarring. Arch. Dermatol. Res. 307, 461–477. doi: 10.1007/s00403-015-1572-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Siedle, B., García-Piñeres, A. J., Murillo, R., Schulte-Mönting, J., Castro, V., Rüngeler, P., et al. (2004). Quantitative structure-activity relationship of sesquiterpene lactones as inhibitors of the transcription factor NF-kappaB. J. Med. Chem. 47, 6042–6054. doi: 10.1021/jm049937r

PubMed Abstract | CrossRef Full Text | Google Scholar

Silva, M. G., Aragão, T. P., Vasconcelos, C. F., Ferreira, P. A., Andrade, B. A., Costa, I. M., et al. (2011). Acute and subacute toxicity of Cassia occidentalis L. stem and leaf in Wistar rats. J. Ethnopharmacol. 136, 341–346. doi: 10.1016/j.jep.2011.04.070

PubMed Abstract | CrossRef Full Text | Google Scholar

Silva, A. A. S., Morais, S. M., Falcão, M. J. C., Vieira, I. G. P., Ribeiro, L. M., Viana, S. M., et al. (2014). Activity of cycloartane-type triterpenes and sterols isolated from Musa paradisiaca fruit peel against Leishmania infantum chagasi. Phytomedicine 21, 1419–1423. doi: 10.1016/j.phymed.2014.05.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Simão da Silva, K. A. B., Klein-Junior, L. C., Cruz, S. M., Cáceres, A., Quintão, N. L. M., Monache, F. D., et al. (2012). Anti-inflammatory and anti-hyperalgesic evaluation of the condiment laurel (Litsea guatemalensis Mez.) and its chemical composition. Food Chem. 132, 1980–1986. doi: 10.1016/j.foodchem.2011.12.036

CrossRef Full Text | Google Scholar

Singh, B., Rastogi, R. P. (1969). Chemical investigation of Asclepias curassavica Lin. Indian J. Chem. 7, 1105–1110.

Google Scholar

Singh, S. G., Nishteswar, K., Patel, B. R., Nariya, M. (2016). Comparative antipyretic and analgesic activities of Cissampelos pareira Linn. and Cyclea peltata (Lam.) Hook. F. & Thomas. Ayu 37, 62–66. doi: 10.4103/ayu.AYU_208_14

PubMed Abstract | CrossRef Full Text | Google Scholar

Smith, B. D. (1997). The initial domestication of Cucurbita pepo in the America 10,000 years ago. Science 276, 932–934. doi: 10.1126/science.276.5314.932

CrossRef Full Text | Google Scholar

Smith-Oka, V. (2008). Plants used for reproductive health by Nahua women in Northern Veracruz, Mexico. Econ. Bot. 62, 604–614. doi: 10.1007/s12231-008-9026-7

CrossRef Full Text | Google Scholar

Sortibrán, A. C., Téllez, M. G. O., Ocotero, V. M., Carballo-Ontiveros, M. A., García, A. M., Valdés, R. J. J., et al. (2011). Chronic toxicity, genotoxic assay, and phytochemical analysis of four traditional medicinal plants. J. Med. Food 14, 1018–1022. doi: 10.1089/jmf.2010.0178

PubMed Abstract | CrossRef Full Text | Google Scholar

Sosa, S., Balick, M. J., Arvigo, R., Esposito, R. G., Pizza, C., Altinier, G., et al. (2002). Screening of the topical anti-inflammatory activity of some Central American plants. J. Ethnopharmacol. 81, 211–215. doi: 10.1016/S0378-8741(02)00080-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Spadaro, F., Costa, R., Circosta, C., Occhiuto, F. (2012). Volatile composition and biological activity of key lime Citrus aurantifolia essential oil. Nat. Prod. Commun. 7, 1523–1526. doi: 10.1177/1934578X1200701128

PubMed Abstract | CrossRef Full Text | Google Scholar

Staub, P. O., Geck, M. S., Weckerle, C. S., Casu, L., Leonti, M. (2015). Classifying diseases and remedies in ethnomedicine and ethnopharmacology. J. Ethnopharmacol. 174, 514–519. doi: 10.1016/j.jep.2015.08.051

PubMed Abstract | CrossRef Full Text | Google Scholar

Stevens, G., Dias, R. H., Thomas, K. J. A., Rivera, J. A., Carvalho, N., Barquera, S., et al. (2008). Characterizing the epidemiological transition in Mexico: National and subnational burden of diseases, injuries, and risk factors. PloS Med. 5, e125. doi: 10.1371/journal.pmed.0050125

PubMed Abstract | CrossRef Full Text | Google Scholar

Stohs, S. J., Preuss, H. G., Shara, M. (2011). The safety of Citrus aurantium (bitter orange) and its primary protoalkaloid p-Synephrine. Phytother. Res. 25, 1421–1428. doi: 10.1002/ptr.3490

PubMed Abstract | CrossRef Full Text | Google Scholar

Stohs, S. J., Preuss, H. G., Shara, M. (2012). A review of the human clinical studies involving Citrus aurantium (bitter orange) extract and its primary orotoalkaloid p-Synephrine. Int. J. Med. Sci. 9, 527–538. doi: 10.7150/ijms.4446

PubMed Abstract | CrossRef Full Text | Google Scholar

Stohs, S. J. (2014). Safety and efficacy of Bixa orellana (achiote, annatto) leaf extracts. Phyther. Res. 28, 956–960. doi: 10.1002/ptr.5088

CrossRef Full Text | Google Scholar

Suppakul, P., Miltz, J., Sonneveld, K., Bigger, S. W. (2003). Antimicrobial properties of basil and its possible application in food packaging. J. Agric. Food Chem. 51, 3197–3207. doi: 10.1021/jf021038t

PubMed Abstract | CrossRef Full Text | Google Scholar

Swargiary, A., Daimari, A., Daimari, M., Basumatary, N., Narzary, E. (2016). Phytochemicals, antioxidant, and anthelmintic activity of selected traditional wild edible plants of lower Assam. Indian J. Pharmacol. 48, 418–423. doi: 10.4103/0253-7613.186212

PubMed Abstract | CrossRef Full Text | Google Scholar

Swerdlin, A., Rainey, D., Storrs, F. J. (2010). Fragrance mix reactions and lime allergic contact dermatitis. Dermatitis 21, 214–216. doi: 10.2310/6620.2010.10014

PubMed Abstract | CrossRef Full Text | Google Scholar

Taddei-Bringas, G. A., Santillana-Macedo, M. A., Romero-Cancio, J. A., Romero-Téllez, M. B. (1999). Acceptance and use of therapeutic medical plants in family medical care. Salud Publica Mex. 41, 216–220. doi: 10.1590/S0036-36341999000300009

PubMed Abstract | CrossRef Full Text | Google Scholar

Tan, B. J., Yap, J. W., Tan, Y. S., Lim, Y. Y., Lee, M. S. (2014). Antioxidant content, antioxidant activity, and antibacterial activity of five plants from the Commelinaceae family. Antioxidants 3, 758–769. doi: 10.3390/antiox3040758

PubMed Abstract | CrossRef Full Text | Google Scholar

Taquira, S., Berger-González, M., Cab, H., Ixcoy, L. (2016). “Tratamientos mayas para el cuerpo, espíritu, mente y sentimiento: El cuidado de la naturaleza cuatripartita del ser,” in Consejo Mayor de Médicos Maya’ob’ por Nacimiento (ed.) Raxnaq’il Nuk’aslemal Medicina Maya en Guatemala (Guatemala: Editorial Cholsamaj).

Google Scholar

Taur, D. J., Waghmare, M. G., Bandal, R. S., Patil, R. Y. (2011). Antinociceptive activity of Ricinus communis L. leaves. Asian Pac. J. Trop. Biomed. 1, 139–141. doi: 10.1016/S2221-1691(11)60012-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Tebbutt, I. H., Teare, A. J., Meek, J. H., Mallett, K. A., Hawkins, D. F. (1984). Caffeine, theophylline and theobromine in pregnancy. Biol. Res. Pregnancy Perinatol. 5, 174–176.

PubMed Abstract | Google Scholar

Terry, R., Posadzki, P., Watson, L. K., Ernst, E. (2011). The use of ginger (Zingiber officinale) for the treatment of pain: a systematic review of clinical trials. Pain Med. 12, 1808–1818. doi: 10.1111/j.1526-4637.2011.01261.x

PubMed Abstract | CrossRef Full Text | Google Scholar

The Angiosperm Phylogeny Group (2016). An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV. Bot. J. Linn. Soc 181, 1–20. doi: 10.1111/boj.12385

CrossRef Full Text | Google Scholar

Thomas, R., Sah, N. K., Sharma, P. B. (2008). Therapeutic biology of Jatropha curcas: A mini review. Curr. Pharm. Biotechnol. 9, 315–324. doi: 10.2174/138920108785161505

PubMed Abstract | CrossRef Full Text | Google Scholar

Treyvaud-Amiguet, V., Arnason, J. T., Maquin, P., Cal, V., Vindas, P. S., Poveda, L. (2005). A consensus ethnobotany of the Q’eqchi’ Maya of Southern Belize. Econ. Bot. 59, 29–42. doi: 10.1663/0013-0001(2005)059[0029:ACEOTQ]2.0.CO;2

CrossRef Full Text | Google Scholar

Triche, E. W., Grosso, L. M., Belanger, K., Darefsky, A. S., Benowitz, N. L., Bracken, M. B. (2008). Chocolate consumption in pregnancy and reduced likelihood of preeclampsia. Epidemiology 19, 459–464. doi: 10.1097/EDE.0b013e31816a1d17

PubMed Abstract | CrossRef Full Text | Google Scholar

Ugarte, C. A. (1997). The ethnopharmacology of plants used as both food and medicine in a Totonac community of Mexico. [MSc thesis] (Miami, USA]: Florida International University).

Google Scholar

Ulbricht, C., Abrams, T. R., Brigham, A., Ceurvels, J., Clubb, J., Curtiss, W., et al. (2010). An Evidence-Based Systematic Review of Rosemary (Rosmarinus officinalis) by the Natural Standard Research Collaboration. J. Diet. Suppl. 7, 351–413. doi: 10.3109/19390211.2010.525049

CrossRef Full Text | Google Scholar

Ulbricht, C., Windsor, R. C., Brigham, A., Bryan, J. K., Conquer, J., Costa, D., et al. (2012). An evidence-based systematic review of annatto (Bixa orellana L.) by the Natural Standard Research Collaboration. J. Diet. Suppl. 9, 57–77. doi: 10.3109/19390211.2012.653530

CrossRef Full Text | Google Scholar

Ulbricht, C., Costa, D., Giese, N., Isaac, R., Liu, A., Liu, Y., et al. (2013). An evidence-based systematic review of bitter orange (Citrus aurantium) by the Natural Standard Research Collaboration. J. Diet. Suppl. 10, 391–431. doi: 10.3109/19390211.2013.830821

CrossRef Full Text | Google Scholar

Ulbricht, C., Basch, E., Cheung, L., Goldberg, H., Hammerness, P., Isaac, R., et al. (2014). An evidence-based systematic review of elderberry and elderflower (Sambucus nigra) by the Natural Standard Research Collaboration. J. Diet. Suppl. 11, 80–120. doi: 10.3109/19390211.2013.859852

CrossRef Full Text | Google Scholar

UN General Assembly (1948). Universal declaration of human rights. New York City, USA: UN General Assembly.

Google Scholar

UN General Assembly (2015). Transforming our world: the 2030 Agenda for Sustainable Development. New York City, USA: UN General Assembly.

Google Scholar

Valdés, A. F. C., Martínez, J. M., Lizama, R. S., Gaitén, Y. G., Rodríguez, D. A., Payrol, J. A. (2010). In vitro antimalarial activity and cytotoxicity of some selected Cuban medicinal plants. Rev. Inst. Med. Trop. Sao Paulo 52, 197–201. doi: 10.1590/S0036-46652010000400006

PubMed Abstract | CrossRef Full Text | Google Scholar

Valdivia-Correa, B., Gómez-Gutiérrez, C., Uribe, M., Méndez-Sánchez, N. (2016). Herbal medicine in Mexico: a cause of hepatotoxicity. A critical review. Int. J. Mol. Sci. 17, 235. doi: 10.3390/ijms17020235

PubMed Abstract | CrossRef Full Text | Google Scholar

Vavilov, N. I. (1992). Origin and geography of cultivated plants (Cambridge: Cambridge University Press).

Google Scholar

Vega Montalvo, R., Lagarto Parra, A. (1999). Evaluación del efecto antiinflamatorio del extracto de Piper auritum H.B.K. y toxicidad aguda oral. Rev. Cuba. Plantas Med. 4, 11–14.

Google Scholar

Velázquez, C., Calzada, F., Torres, J., González, F., Ceballos, G. (2006). Antisecretory activity of plants used to treat gastrointestinal disorders in Mexico. J. Ethnopharmacol. 103, 66–70. doi: 10.1016/j.jep.2005.06.046

PubMed Abstract | CrossRef Full Text | Google Scholar

Venâncio, A. M., Onofre, A. S. C., Lira, A. F., Alves, P. B., Blank, A. F., Antoniolli, Â. R., et al. (2011). Chemical composition, acute toxicity, and antinociceptive activity of the essential oil of a plant breeding cultivar of Basil (Ocimum basilicum L.). Planta Med. 77, 825–829. doi: 10.1055/s-0030-1250607

PubMed Abstract | CrossRef Full Text | Google Scholar

Vidal, A., Fallarero, A., Peña, B. R., Medina, M. E., Gra, B., Rivera, F., et al. (2003). Studies on the toxicity of Punica granatum L. (Punicaceae) whole fruit extracts. J. Ethnopharmacol. 89, 295–300. doi: 10.1016/j.jep.2003.09.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Vidotti, G. J., Zimmermann, A., Sarragiotto, M. H., Nakamura, C. V., Dias Filho, B. P. (2006). Antimicrobial and phytochemical studies on Pedilanthus tithymaloides. Fitoterapia 77, 43–46. doi: 10.1016/j.fitote.2005.08.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Vogler, B. K., Ernst, E. (1999). Aloe vera: a systematic review of its clinical effectiveness. Br. J. Gen. Pract. 49, 823–828.

PubMed Abstract | Google Scholar

Waldstein, A. (2006). Mexican migrant ethnopharmacology: Pharmacopoeia, classification of medicines and explanations of efficacy. J. Ethnopharmacol. 108, 299–310. doi: 10.1016/j.jep.2006.07.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Walshe-Roussel, B., Choueiri, C., Saleem, A., Asim, M., Caal, F., Cal, V., et al. (2013). Potent anti-inflammatory activity of sesquiterpene lactones from Neurolaena lobata (L.) R. Br. ex Cass., a Q’eqchi’ Maya traditional medicine. Phytochemistry 92, 122–127. doi: 10.1016/j.phytochem.2013.05.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, H., Zhao, M., Yang, B., Jiang, Y., Rao, G. (2008). Identification of polyphenols in tobacco leaf and their antioxidant and antimicrobial activities. Food Chem. 107, 1399–1406. doi: 10.1016/j.foodchem.2007.09.068

CrossRef Full Text | Google Scholar

Wang, C., Zhang, T., Liu, J., Lu, S., Zhang, C., Wang, E., et al. (2011). Subchronic toxicity study of corn silk with rats. J. Ethnopharmacol. 137, 36–43. doi: 10.1016/j.jep.2011.03.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Wei, L., Li, Z., Chen, B. (2000). Clinical study on treatment of infantile rotaviral enteritis with Psidium guajava L. Zhongguo Zhong Xi Yi Jie He Za Zhi 20, 893–895. doi: 10.1007/BF02935007

PubMed Abstract | CrossRef Full Text | Google Scholar

Wei, J.-N., Liu, Z.-H., Zhao, Y.-P., Zhao, L.-L., Xue, T.-K., Lan, Q.-K. (2019). Phytochemical and bioactive profile of Coriandrum sativum L. Food Chem. 286, 260–267. doi: 10.1016/j.foodchem.2019.01.171

PubMed Abstract | CrossRef Full Text | Google Scholar

Weimann, C., Heinrich, M. (1997). Indigenous medicinal plants in Mexico: the example of the Nahua (Sierra of Zongolica). Bot. Acta 110, 62–72. doi: 10.1111/j.1438-8677.1997.tb00612.x

CrossRef Full Text | Google Scholar

Weimann, C. (2000). Ethnobotanik der Nahua der Sierra de Zongolica, Veracruz, Mexico und phytochemisch-biologische Untersuchungen von Baccharis conferta Kunth (Asteraceae). [PhD dissertation] (Freiburg, Germany: University of Freiburg).

Google Scholar

Weller, S. C., Baer, R. D., de Alba Garcia, J. G., Glazer, M., Trotter, R., Pachter, L., et al. (2002). Regional variation in Latino descriptions of susto. Cult. Med. Psychiatry 26, 449–472. doi: 10.1023/A:1021743405946

PubMed Abstract | CrossRef Full Text | Google Scholar

Weniger, B. (1991). Interest and limitation of a global ethnopharmacological survey. J. Ethnopharmacol. 32, 37–41. doi: 10.1016/0378-8741(91)90101-I

PubMed Abstract | CrossRef Full Text | Google Scholar

Wesseling, C., Crowe, J., Hogstedt, C., Jakobsson, K., Lucas, R., Wegman, D.H. (2013). The epidemic of chronic kidney disease of unknown etiology in Mesoamerica: A call for interdisciplinary research and action. Am. J. Public Health 103, 1927–1930. doi: 10.2105/AJPH.2013.301594

PubMed Abstract | CrossRef Full Text | Google Scholar

Wesseling, C., Glaser, J., Rodríguez-Guzmán, J., Weiss, I., Lucas, R., Peraza, S., et al. (2020). Chronic kidney disease of non-traditional origin in Mesoamerica: a disease primarily driven by occupational heat stress. Rev. Panam Salud Publica. 44, e15. doi: 10.26633/RPSP.2020.15 eCollection 2020.

PubMed Abstract | CrossRef Full Text | Google Scholar

WHO (1996). Expert Committee on specifications for pharmaceutical preparations: Thirty-fourth report (Geneva: World Health Organization).

Google Scholar

WHO (1998). Guidelines for the Appropriate Use of Herbal Medicines (Manila: WHO Regional Office for the Western Pacific).

Google Scholar

WHO (2005). National policy on traditional medicine and regulation of herbal medicines: report of a WHO global survey (Geneva: World Health Organization).

Google Scholar

WHO (2013). Traditional Medicine Strategy 2014-2023 (Geneva: World Health Organization).

Google Scholar

Wiart, C., Mogana, S., Khalifah, S., Mahan, M., Ismail, S., Buckle, M., et al. (2004). Antimicrobial screening of plants used for traditional medicine in the state of Perak, Peninsular Malaysia. Fitoterapia 75, 68–73. doi: 10.1016/j.fitote.2003.07.013

PubMed Abstract | CrossRef Full Text | Google Scholar

WICC (Wonca International Classification Committee) (2004). International Classification of Primary Care (ICPC-2). Available at: http://www.kith.no/upload/2705/icpc-2-english.pdf (Accessed May, 05, 2016).

Google Scholar

Wichtl, M. (2004). Herbal Drugs and Phytopharmaceuticals. 3rd ed. (Boca Raton: CRC Press).

Google Scholar

Wijkström, J., Leiva, R., Elinder, C. G., Leiva, S., Trujillo, Z., Trujillo, L., et al. (2013). Clinical and pathological characterization of Mesoamerican nephropathy: a new kidney disease in Central America. Am. J. Kidney Dis. 62, 908–918. doi: 10.1053/j.ajkd.2013.05.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Willcox, M. L., Graz, B., Falquet, J., Diakite, C., Giani, S., Diallo, D. (2011). A “reverse pharmacology” approach for developing an anti-malarial phytomedicine. Malar J. 10 (Suppl 1), S8. doi: 10.1186/1475-2875-10-S1-S8

PubMed Abstract | CrossRef Full Text | Google Scholar

Witt, C. M. (2013). Clinical research on traditional drugs and food items–the potential of comparative effectiveness research for interdisciplinary research. J. Ethnopharmacol. 147, 254–258. doi: 10.1016/j.jep.2013.02.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Worbs, S., Köhler, K., Pauly, D., Avondet, M.-A., Schaer, M., Dorner, M. B., et al. (2011). Ricinus communis intoxications in human and veterinary nedicine-A summary of real cases. Toxins 3, 1332–1372. doi: 10.3390/toxins3101332

PubMed Abstract | CrossRef Full Text | Google Scholar

World Bank (2016). Guatemala: Estudio Institucional y de Gasto Social. Available at: http://documents.worldbank.org/curated/pt/287571481093188052/pdf/110778-WP-P158442-PUBLIC-SPANISH-SSEIRGuatemalaSpanish.pdf (Accessed May, 23, 2020).

Google Scholar

Yadav, J. P., Arya, V., Yadav, S., Panghal, M., Kumar, S., Dhankhar, S. (2010). Cassia occidentalis L.: a review on its ethnobotany, phytochemical and pharmacological profile. Fitoterapia 81, 223–230. doi: 10.1016/j.fitote.2009.09.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Yakubu, M. T., Salimon, S. S. (2015). Antidiarrhoeal activity of aqueous extract of Mangifera indica L. leaves in female albino rats. J. Ethnopharmacol. 163, 135–141. doi: 10.1016/j.jep.2014.12.060

PubMed Abstract | CrossRef Full Text | Google Scholar

Yamthe, L. R. T., Fokou, P. V. T., Mbouna, C. D. J., Keumoe, R., Ndjakou, B. L., Djouonzo, P. T., et al. (2015). Extracts from Annona muricata L. and Annona reticulata L. (Annonaceae) potently and selectively inhibit Plasmodium falciparum. Medicines 2, 55–66. doi: 10.3390/medicines2020055

PubMed Abstract | CrossRef Full Text | Google Scholar

Yartey, J., Nkrumah, F., Hori, H., Harrison, K., Amrmar, D. (1995). Clinical trial of fermented maize-based oral rehydration solution in the management of acute diarrhoea in children. Ann. Trop. Paediatr. 15, 61–68. doi: 10.1080/02724936.1995.11747750

PubMed Abstract | CrossRef Full Text | Google Scholar

Yasunaka, K., Abe, F., Nagayama, A., Okabe, H., Lozada-Pérez, L., López-Villafranco, E., et al. (2005). Antibacterial activity of crude extracts from Mexican medicinal plants and purified coumarins and xanthones. J. Ethnopharmacol. 97, 293–299. doi: 10.1016/j.jep.2004.11.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Ye, H., Liu, Y., Li, N., Yu, J., Cheng, H., Li, J., et al. (2015). Anti-Helicobacter pylori activities of Chenopodium ambrosioides L. in vitro and in vivo. World J. Gastroenterol. 21, 4178–4183. doi: 10.3748/wjg.v21.i14.4178

PubMed Abstract | CrossRef Full Text | Google Scholar

Yen, G. C., Chen, H. Y., Peng, H. H. (2001). Evaluation of the cytotoxicity, mutagenicity and antimutagenicity of emerging edible plants. Food Chem. Toxicol. 39, 1045–1053. doi: 10.1016/S0278-6915(01)00053-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Yousaf, Z., Wang, Y., Baydoun, E. (2013). Phytochemistry and pharmacological studies on Solanum torvum Swartz. J. Appl. Pharm. Sci. 3, 152–160. doi: 10.7324/JAPS.2013.3428

CrossRef Full Text | Google Scholar

Zachariah, S. M., Viswanad, V., Aleykutty, N. A., Jaykar, B., Halima, O. A. (2012). Free radical scavenging and antibacterial activity of Mirabilis jalapa Linn using in vitro models. Asian J. Pharm. Clin. Res. 5, 115–120.

Google Scholar

Zamora-Martínez, M. C., de Pascual Pola, C. N. (1992). Medicinal plants used in some rural populations of Oaxaca, Puebla and Veracruz, Mexico. J. Ethnopharmacol. 35, 229–257. doi: 10.1016/0378-8741(92)90021-I

PubMed Abstract | CrossRef Full Text | Google Scholar

Zeichen de Sa, R., Rey, A., Argañaraz, E., Bindstein, E. (2000). Perinatal toxicology of Ruta chalepensis (Rutaceae) in mice. J. Ethnopharmacol. 69, 93–98. doi: 10.1016/S0378-8741(98)00232-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, L., Lokeshwar, B. L. (2012). Medicinal properties of the Jamaican pepper plant Pimenta dioica and allspice. Curr. Drug Targets 13, 1900–1906. doi: 10.2174/138945012804545641

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Mesoamerican traditional medicine, evidence-based phytotherapy, universal health coverage, medicinal plants, Mexico, Central America

Citation: Geck MS, Cristians S, Berger-González M, Casu L, Heinrich M and Leonti M (2020) Traditional Herbal Medicine in Mesoamerica: Toward Its Evidence Base for Improving Universal Health Coverage. Front. Pharmacol. 11:1160. doi: 10.3389/fphar.2020.01160

Received: 07 March 2020; Accepted: 16 July 2020;
Published: 31 July 2020.

Edited by:

Hung-Rong Yen, China Medical University, Taiwan

Reviewed by:

Armando Caceres, Universidad de San Carlos de Guatemala, Guatemala
Tinde Van Andel, Naturalis Biodiversity Center, Netherlands

Copyright © 2020 Geck, Cristians, Berger-González, Casu, Heinrich and Leonti. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Marco Leonti, bWFyY29sZW9udGlAbmV0c2NhcGUubmV0; bWxlb250aUB1bmljYS5pdA==

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