Skip to main content

REVIEW article

Front. Pharmacol., 26 May 2020
Sec. Ethnopharmacology
This article is part of the Research Topic Medicinal Plants for Cardiovascular and Neurodegenerative Aging-related Diseases: From Bench to Bedside View all 20 articles

Aniba canelilla (Kunth) Mez (Lauraceae): A Review of Ethnobotany, Phytochemical, Antioxidant, Anti-Inflammatory, Cardiovascular, and Neurological Properties

  • 1Laboratório de Farmacologia da Inflamação e do Comportamento, Universidade Federal do Pará, Belém-PA, Brazil
  • 2Programa de Pós-Graduação em Ciências Farmacêuticas, Instituto de Ciências da Saúde, Universidade Federal do Pará, Belém-PA, Brazil

Aniba canelilla (Kunth) Mez, popularly known as “casca preciosa” (precious bark), falsa canela (cinnamon-scented) Casca-do-maranhão (bark of maranhão), and Folha-preciosa (precious leaf), is an aromatic species of the Lauraceae family, widely distributed in the Amazon region. In traditional medicine, it is indicated for the treatment of a great diversity of diseases, including digestive, respiratory, inflam]matory, painful, and central nervous system disorders, it is administered mainly in the form of tea or decoction orally. Its essential oil is referred to as a natural antioxidant for food preservation and disease control, showing great potential for use in the cosmetics, perfumery, and pharmaceutical products sector. The present review aimed to discuss critically and comprehensively the ethnobotanical characteristics, phytochemical constitution, and scientifically tested biological properties of A. canelilla, systematizing the knowledge about the species and proposing new perspectives for research and development. The chemical composition of A. canelilla includes 1-nitro-2-phenylethane, metyleugenol, eugenol, safrol, anabasin, anbin, tannin, α-pinene, b-pinene, b-felandren, b-caryophyllene, b-sesquifelandren, p-cymene, linalool, α-copaene, and spatulenol. Researches with ethanolic extracts, essential oils, and major constituents (1-nitro-2-phenylethane and metyleugenol) have revealed antioxidant, antinociceptive, anti-inflammatory, cardio-modulating, hypotensive (vasorelaxant), hypnotic, anxiolytic, anticholinesterase, and antibiotic properties (trypanomicidal, leishmanicidal, and antifungal). Some of these effects are potentially beneficial for aging-related diseases treatment, such as cardio and cerebrovascular, chronic inflammatory, neurological, and degenerative diseases. However, it is necessary to advance in the research of its clinical use and development of therapeutic products.

Introduction

The increase in human longevity, as well as population growth, is a result of its social and technological evolution. This phenomenon, however, represents a growing public health challenge due to the proportional increase in the incidence of chronic inflammatory, neurological, and cardiovascular diseases. Such pathological conditions often require chronic polymedication which are sometimes marked by intense adverse reactions and are not always effective, leading to deterioration of patients' quality of life or discontinuation of therapy. There are still cases where current therapy consists only of palliative measures, with little effect on disease progression (Boccardi, 2019). This reality drives the scientific community in search of safer and more effective drugs.

Finding a solution for the future, however, may be related to our ability to investigate the past, valuing all traditional knowledge about plant species with therapeutic potential but lacking studies on their safety and effectiveness. In fact, medical plants have been a valuable source of herbal medicines and bioactive molecules for drug development (Samy et al., 2008). Brazilian forests, especially the Amazon rainforest, represent the largest source of plant species in the world, many of which have medicinal benefits. Along with such biodiversity, the Brazilian population also has a very rich folk medicine, preserved by traditional communities, which provides valuable information, useful to the selection of species for pharmacological screening (Hegde et al., 2014; Moraes et al., 2019).

Among the plants inserted in the Amazonian culture, Aniba canelilla (Kunth) Mez [syn. Aniba elliptica A.C. Sm., Cryptocarya canelilla Kunth, and others] stands out for its diversity economic and medicinal applications. This species of Lauraceae is an aromatic medium-sized tree, native from solid ground and semi-deciduous forests of South America, known as casca-preciosa (precious bark), falsa-canela (fake cinnamon), casca-do-maranhão (maranhão bark), and folha-preciosa (precious leaf), (Gottlieb and Magalhães, 1960b; Kubitzki and Renner, 1982; Ribeiro et al., 1999; Franciscon et al., 2018; Tropicos.org, 2019). Among its characteristics, the cinnamon-like aroma stands out, is even linked to the history of its discovery. Around Brazil discovery period, when Portuguese and Spanish navigators entered the Amazon River in search of cinnamon (Cinnamomum verum J.Presl) thought they had found a lot of this plant, instead what they had found was Casca-preciosa trees (Pinto, 1995). In folk medicine, this species is often used to treat painful and inflammatory conditions, gastrointestinal disorders, and neurological and psychiatric diseases, in addition to the treatment of infections (Maia et al., 2001; De Filipps et al., 2004; Sousa et al., 2009; Manhães et al., 2012). Some of these applications have been studied, elucidating their main constituents and ratifying their anti-inflammatory, antinociceptive, antihypertensive, and antioxidant potential, among others.

Nevertheless, it is noted that much remains to be elucidated about the therapeutic potential of A. canelilla, including the safety of its use, medical applications, and mechanisms of action. In this sense, the present study aims to review critically and comprehensively the current knowledge about the ethnobotany, phytochemical, pharmacological, and toxicological characteristics of A. canelilla and its derivatives (extracts, essential oil, and major constituents), identifying perspectives for new research and exploring its potential for neurological and cardiovascular diseases treatment (Graphical abstract—Figure S1). Data collection on A. canelilla was carried out electronically, based on articles published in peer-reviewed journals, abstracts published in conference proceedings, theses, and ethnobotanical textbooks. The research was carried out in the Google Scholar, Science Direct, Scopos, and PubMed databases.

Ethnobotany

Taxonomy and Botanical Aspects

Lauraceae is a family of trees and shrubs recorded since the Cretaceous period, which includes 52 genera and approximately 2,500 to 3,500 species, distributed in tropical and subtropical areas, as well as in temperate climates, as America, tropical Asia, Australia, and Madagascar (Van der Werff, 1991; Kubitzki et al., 1993; Hu et al., 2007). This family gathers medium to large trees, but some species have characteristics of shrubs or small trees, with a diameter between 1 and 5 cm and their height rarely exceeds 8 m (Ribeiro et al., 1999). Several species of Lauraceae have economic use, providing wood, essential oils, and chemical compounds, relevant to civil construction and for the food and pharmaceutical industries (Barbosa et al., 2012). In Brazil, 24 genera and 441 species have been identified (Quinet et al., 2015). Some genera of Lauraceae are highlighted by having aromatic species, that is, plants that produce essential oils (EO) or resins rich in volatile compounds, as Aniba, Nectandra, Ocotea, Licaria, and Dicypellium (Marques, 2001).

As previously mentioned, the species A. canelilla is an aromatic plant with a characteristic odor, which is easily confused with cinnamon. Historically this characteristic is portrayed in the expeditions of Pizzarro and Orellana, in 1540, to the Amazon River, and Humbolt and Bonpland to the Orinoco River in 1800. In both cases, it was considered that excellent sources of the coveted spice were found, when in fact they found Casca-preciosa (Naranjo et al., 1981; Pinto, 1995; Lahlou et al., 2005). Its proper botanical designation was made by Carl Kunth, a German botanist, from samples collected by Humbolt and Bonpland. In his description, the botanist emphasized the aromatic characteristic of the plant and its similarity to cinnamon. Initially called Aniba canelilla by Kunth, it was later registered and published by Carl Mez (1889), being officially identified as Aniba canelilla (Kunth) Mez (Gottlieb and Magalhães, 1960b; Almeida et al., 2017).

This prominent tree reaches up to 35 m in height and has a retinal trunk, with a diameter between 40 and 60 cm. Its branches are glabrous and lenticelated, with 8 to 16 cm leaves (thin petioles, grayish and dense garment, and secondary veins flattened and slightly prominent at the bottom), small flowers, and oblong capsular fruit (De Siqueira et al., 2010).

Distribution and Traditional Uses

Native to the plains and solid ground forests of the Amazon rainforest and Guyana, A. canelilla is adaptable to different types of soils, including regions of solid or semi-deciduous forests, lowland areas, rocky outcrops and rocky soils, poorly drained soils, and clay and sandy soils (Franciscon et al., 2018). This species extends from the Antilles, Guyana high lands to the dry lands of Brazil. In fact, it presents a wide distribution in the Amazon region, which predominates from the East of French Guiana, Suriname, Venezuela, Colombia to the Peruvian Amazon, rarely found in Central America (Kubitzki and Renner, 1982; Van der Werff, 1991; Ribeiro et al., 1999; Quinet et al., 2015; Figure 1). Table 1 summarizes the various popular names attributed to A. canelilla, by geographic location.

FIGURE 1
www.frontiersin.org

Figure 1 Distribution of Aniba canelilla in South America. Blue color in cartogram indicates coutries where the A. canelilla tree is native, Orange color indicates countries where its native presence is doubtful, and the dark green color highlights the states of Brazil where it is native. Adapted from Quinet et al., 2015.

TABLE 1
www.frontiersin.org

Table 1 Popular names of Aniba canelilla according to its geographical location.

A. canelilla is present in several aspects of the culture of these peoples. Its wood is used for civil construction (Lupe, 2007) and its EO and extracts are consumed as spices, cosmetics, and perfumes, as the product known as “Cheiro-de-santarém” (Maia et al., 2011; Araújo et al., 2007; Lorenzi and Matos, 2008; Barbosa et al., 2017).

In folk medicine, multiple ethnopharmacological indications have been found, with variations in the form of use. The most frequently mentioned form was the infusion of the barks, used to treat stomach inflammation, pain, and ulcers (De Almeida et al., 2013). Interestingly, the plant has been cited as a natural soothing, and still cited by indigenous communities as tranquilizer (Oger et al., 1994; Almeida et al., 2013; Santos et al., 2016), in contrast to some studies that point a stimulating and antidepressant effect (Rodrigues and Carlini, 2006; Bitencourt et al., 2014). There were also indications for the treatment of colds, cough, headache, and nausea (Taylor, 2005). Topical applications of bark extracts have been cited for the treatment of skin diseases, injuries, and infections (Mors et al., 2000; Taylor, 2005). A. canelilla EO (AcEO) also has a wide range of indications. According to Barbosa et al. (2017), the AcEO has therapeutic properties similar to those attributed to the infusions of bark, leaves, and branches, and there are also citations of its use to treat acne, dermatitis, fever, and various types of infections and injuries (Taylor, 2005). Another interesting finding is the use of smoke produced by barks burning, by the Tiryó Indians (Suriname), to treat diarrhea (De Filipps et al., 2004). References of the use of this species as analgesic, anti-inflammatory, antispasmodic, anti-anemic, anti-dysenteric, and antibiotic are also frequent. Additional uses of A. canelilla in folk medicine are summarized in Table 2.

TABLE 2
www.frontiersin.org

Table 2 Traditional uses of Aniba canelilla.

Phytochemical Composition

Extracts

There are few studies dedicated to elucidate the phytochemical composition of A. canelilla extracts and carried out studies present only screens of the metabolite classes. For example, the study conducted by Mesquita et al. (2014) demonstrated the presence of phenolic compounds, tannins, flavonoids, and saponins in ethanol extracts obtained from leaves and branches. Despite the typical presence of benzyltetrahydroisoquinoline alkaloids in Lauraceae species, such as reticulin, coclaurine, and noranicanine (Oger et al., 1992; Oger et al., 1993; Custódio and Veiga Junior, 2014), the evaluation of the ethanolic extracts of A. canelilla did not detect alkaloids, as well as steroids and triterpenes.

Essential Oil

AcEO, unlike other extracts, has been well characterized. It is a yellowish-brown oil, denser than water, which have the characteristic aroma of the specie. It can be extracted from the trunk wood, branches, leaves, thin stems, and barks, by steam distillation or hydrodistillation, using a Clevenger-type apparatus, with a yield between 0.2 to 1.3% (Gottlieb and Magalhães, 1960a; Oger et al., 1994; Taveira et al., 2003; Da Silva et al., 2007; Silva et al., 2009; Silva et al., 2014; Barbosa et al., 2017; Giongo et al., 2017). Several factors, such as humidity and incidence of light, physiological, and geographical variations, environmental conditions, and genetic factors, can influence the production of AcOE. The available studies demonstrate higher oil yield in rainy periods, in the initial periods of development of plant organs, and in conditions where there is a greater supply of light. Regarding the parts of the plant, its yield of the stem is higher in the dry seasons. Leaf yield, however, does not appear to be influenced by such factors (Taveira et al., 2003; Manhães et al., 2012).

Its chemical composition has two main constituents, 1-nitro-2-phenylethane (1N2PE), the first known natural nitro derivative which is generally pointed as the major component and is responsible for the cinnamon-like odor characteristic of the species, and methyleneugenol (Gottlieb and Magalhães, 1959; Gottlieb and Magalhães, 1960a; Oger et al., 1994; Maia et al., 2001; Taveira et al., 2003; Lima et al., 2004; Da Silva et al., 2007; Maia and Andrade, 2009; Silva et al., 2009; Sousa, 2011; Manhães et al., 2012; Vale et al., 2013; Almeida et al., 2017; Farias et al., 2017; Giongo et al., 2017). These substances were identified both in the stem wood, bark, and leaves. Other identified constituents are eugenol, safrole, anabasine, anbin, tannin, α-pinene, b-pinene, b-felandren, b-caryophyllene, b-sesquifelandren, p-cymene, linalool, α-copaene, and spatulenol (Sangwan et al., 2001; Figueiredo et al., 2008). The main chemical constituents present in AcEO are listed in Figure 2.

FIGURE 2
www.frontiersin.org

Figure 2 Substances present in the Aniba canelilla essential oil: 1-nitro-2-phenylethane (A), methyleugenol (B), eugenol (C), linalool (D), safrole (E), α-pinene (F), β-pinene (G), benzaldehyde (H). Adapted from: Sugimoto et al. (2017), Sipe et al. (2014), Tsuchiya (2017), Rianjanu et al. (2018), Silva et al. (2012).

As well as the oil yield, its composition also suffers seasonal influence. In the rainy period, the 1N2PE concentrations reach near 95%, while methyleugenol remain below 18%. In the dry period, 1N2PE decrease to less than 40%, while methyleugenol reaches 45%. The greatest value of 1N2PE (95.3%) and the least value of methyleugenol (0.2%) were observed in the leaves, during the rainy season (Taveira et al., 2003). Silva et al. (2009), otherwise, found no variation in 1N2PE concentration from the rainy to the dry seasons in samples collected on Reserva Adolpho Ducke, AM, Brazil. Additionally, methyleugenol was not detected in oils (Silva et al., 2009). Regarding the parts of the plant, Taveira et al. (2003) has found higher percentage of 1N2PE in leaves, while Manhães et al. (2012) found higher concentrations in stems. The content of 1N2PE and methyleugenol in leaves and fine stems are comparable to the content observed in the trunk wood and bark of A. canelilla. Thus, the extraction of essential oil from leaves and branches becomes an alternative to prevent the overthrow of the trunk to produce essential oils from this specie (Barbosa et al., 2017).

1-Nitro-2-Phenylethane

1N2PE (C8H9NO2, MW 151.16) is a nitro compound formed through the biotransformation of phenylalanine by enzymes of the CYP superfamily (cytochrome P450) (Gottlieb and Magalhães, 1959; Gottlieb, 1972; Matsuo et al., 1972; Wittstock and Halkier, 2000). It is also found in two other species, Ocotea pretiosa (Nees & Mart.) Mez (Lauraceae) (Gottlieb and Magalhães, 1959), present in São Paulo, Rio de Janeiro, Minas Gerais and Santa Catarina (Brazil) states, where it is known as Canela-sassafrás, and Dennettia tripetala G. Baker (Annonaceae) (Okogun and Ekong, 1969; Oyemitan et al., 2013). Due to the characteristic odor generated by the nitro compound, O. pretiosa can be confused with A. canelilla. EO samples from O. pretiosa collected in the warmer regions Brazilian southeastern showed 1N2PE and methyleugenol with main constituents (Gottlieb and Magalhães, 1959), while samples collected in the south, colder region, showed higher proportions of safrole (Gottlieb and Magalhães, 1960a).

Methyleugenol

Chemically referred to as 1-allyl-3,4-dimethoxybenzene (C11H14O2, MW 178.23), methyleugenol is a yellowish oily compound with the characteristic of clove aroma and bitter taste, present in a wide variety of EOs. It is soluble in several organic solvents and insoluble in water. Methyleugenol is formed from the methylation of eugenol, another minor phenolic compound found in the AcEO (Gottlieb and Magalhães, 1959; Lahlou et al., 2004; Burdock, 2005; Barbosa et al., 2017). Concerning its occurrence in the parts of the plant, it is mainly concentrated in the trunk wood, where it has already been quantified at the concentration of 45.8% (Taveira et al., 2003). In the state of Pará, Brazil, it is considered a chemical marker for the AcEO, is also a significant constituent in other Lauraceae species, such as O. pretiosa from Southeastern Brazilian States (Gottlieb and Magalhães, 1960a; Silva et al., 2009; Manhães et al., 2012).

Biological Properties

Traditional communities attribute a variety of therapeutic properties to A. canelilla, being applied to the treatment of painful and inflammatory conditions, gastrointestinal and respiratory diseases, microbial infections, and parasitosis, in addition to neuropsychiatric disorders, as detailed above. Therefore, based on the medicinal culture of these people, much has been explored in scientific research, even though most of these studies have little depth. The studies identified in this review addressed mainly the toxicity antioxidant, antinociceptive, anti-inflammatory, cardiovascular, and neuropharmacological activities of A. canelilla EO and extracts in murine or in vitro models. Evidence of anticholinesterase and antibiotic activity was also verified (Table 3).

TABLE 3
www.frontiersin.org

Table 3 Biological activities of Aniba Canelilla extracts, essential oil, and 1-nitro-2-phenylethane.

Toxicity

Characterizing the safety of using a therapeutic agent is as important as ensuring its effectiveness, being a requirement for the registration of herbal agents. The present review identified in vitro, and in vivo toxicological tests that aimed to characterize acute and subacute toxicity of A. canelilla derived products.

The cytotoxicity of AcEO and its two main constituents was tested by Giongo et al. (2017) in primary lymphocyte culture. AcEO, 1N2PE, and methyleugenol were tested in concentrations of 0.5%, 1%, and 2%, producing no cytotoxicity on those cells. However, the samples treated with a mixture of 1N2PE and methyleugenol in the concentration of 2% showed an average reduction of 21% in cell viability, pointing to the potential risk of the association of these constituents in high concentrations. In the brine shrimp bioassay, Silva et al. (2007) performed the analysis of plant samples collected in the Brazilian states of Para and Amazonas in rainy season. Methanolic extracts and EO from the trunks wood were tested, as well as 1N2PE isolated from EO. Products presented medium lethal concentration (LC50) of 91.38 ± 7.20 μg/mL, 21.61 ± 1.21 μg/mL, and 20.37 ± 0.99 μg/mL, respectively, highlighting that 1N2PE showed equivalent activity to EO, and methanolic extract presented toxicity about four times lower.

AcEO oral toxicity was tested in an acute and subacute pattern of administration in murine models by Sousa et al. (2009). In the acute evaluation, performed with mice, the authors presented a medium lethal dose (LD50) of 720 ± 66.4 mg/kg, despite declaring that the “study does not show any toxic symptoms, changes in behavior or mortality at the tested doses.” For 1N2PE, LD50 of 712 ± 17.39 mg/kg for oral administration (Lima, 2008) and 490 mg/kg for intraperitoneal (ip) administration were identified in mice (Oyemitan et al., 2013).

Subacute toxicity (30 days of treatment) was tested in rats, with doses equivalent to 5% (36 mg/kg) and 10% (72 mg/kg) of LD50, evaluating the incidence of deaths and behavioral, hematological (red cells, hematocrit, hemoglobin, MCV, HCM, MCCH, leukocytes, segmented cells, lymphocytes, and monocytes), biochemical (glucose, urea, creatinine, triglycerides, cholesterol, ALT, AST, and alkaline phosphatases), and histopathological markers. AcEO did not promote deaths in tested doses, nor did it promote significant changes in animals' behavior, as well as in the biochemical and hematological parameters tested. The vital organs showed no histological changes, except for the liver, which presented necrotic foci, apoptotic cells, and mononuclear infiltrate. There was also evidence of tissue regeneration, which, together with the absence of changes in biochemical markers, indicates adaptation of the organ to aggression. Together, these findings classify AcEO and 1N2PE as class 4 xenobiotics (low toxicity) (OECD, 2001).

Antioxidant Activity

The genesis and evolution of chronic degenerative diseases, as well as several pathologies, are strongly related to the imbalance between reactive oxygen species (ROS) production and the body's enzymatic and non-enzymatic antioxidant agents, a state called oxidative stress. Several EOs are recognized for their antioxidant potential, used for food preservation, but it also has pharmaceutical interest (Ruberto and Baratta, 2000; Miliauskas et al., 2004; Mimica-Duric et al., 2004). Such properties have been associated with the presence of phenolic compounds, such as flavonoids, phenolic acids, and phenolic diterpenes in aromatic plants. Studies carried out with A. canelilla highlight its potential, related to the presence of antioxidant phenolic compounds and coumarins, for the development of cosmetic, anti-corrosion products for the metallurgical industry and pharmaceutical products (Da Silva et al., 2007; Silva, 2012; Mesquita et al., 2014; Farias et al., 2017; Barros et al., 2018).

Despite the potential of its phytochemical constituents, until now only chemical tests have been used to evaluate the antioxidant capacity of A. canelilla derivatives, based on its ability to eliminate DPPH (2,2-diphenyl-1-picrylhydrazyl) radicals, an assay aimed to screen non-enzymatic antioxidant agents candidate scavenger activity, using the Trolox (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid), ascorbic acid, and/or quercetin as activity patterns. Da Silva et al. (2007), using Trolox as standard, demonstrated an DPPH inhibition of 32 to 93% for samples of AcEO (110 to 1,400 µg/mL) obtained from Amazonas and Pará state (Brazil) plants. Methanolic extracts (2 to 10 µg/mL) obtained from same plants showed an DPPH inhibition of 25 to 93%, and 11.47 to 63.19% of inhibition was found for 1N2PE (200 to 1000 µg/mL). Such findings suggest a greater antioxidant capacity for the methanolic extract, up to fifty times higher than that of AcEO and equivalent to Trolox. For ethanolic extract of the plant branches and leaves, Mesquita et al. (2014) demonstrated a greater scavenger activity in leaf extract, that showed 34.97% of ascorbic acid activity. This finding was similar to the one found by Silva (2012), who noticed that the ethanolic extract of the leaves had about one-third of ascorbic acid activity. In the same study, the hydroalcoholic extract presented similar results. The results by Martins et al. (2016), on the other hand, demonstrated equivalence between ascorbic acid and the ethanolic extract from the bark of A. canelilla. They also demonstrated that the extracts had photoprotective effect.

In this context, considering the preliminary character of these findings and the identification of secondary metabolites, phenolic compounds, and coumarins, related to antioxidant activity and the reduction of the risk of various diseases, in products obtained from A. canelilla (Bubols et al., 2013; Mesquita et al., 2014; Serino and Salazar, 2019), we believe it is essential to explore biological models to evaluate its effects on enzymes with oxidizing [nicotinic adenine dinucleotide phosphate oxidase (NOX), nitric oxide synthase (NOS), monoxides, and xanthine oxidoreductase (XO), etc.] and antioxidant [catalase, glutathione (GPx), superoxide dismutase (SOD), etc.] activities, as well as on the formation of ROS and oxidative injury markers (lipid peroxidation, carbonylated proteins, etc.) (Awad et al., 2018) to determine its real benefit for the prevention or treatment of chronic and/or degenerative metabolic, cardiovascular, neural, and other diseases, whose mechanisms of genesis and evolution comprise of an important oxidative component (for review: Uttara et al., 2009; Liguori et al., 2018).

Antinociceptive and Anti-Inflammatory Activity

Inflammation is another key pathophysiological process in the origin and development of numerous diseases. Considering not only the chronic inflammatory conditions that are increasing in function of aging, but it has also been widely discussed in cardiovascular and neuropsychiatric diseases context, showing clinical benefits with anti-inflammatory drugs use. Pain is involved in worsening the patient's quality of life, requiring non-pharmacological and pharmacological care aimed at its adequate control. In this context, A. canelilla has shown promise, since published studies have ratified, in murine models, its antinociceptive and anti-inflammatory properties referred in traditional use.

The study initially conducted by Lima (2008), later expanded and published in two other articles (Lima et al., 2009; Vale et al., 2013), demonstrated antinociceptive and anti-inflammatory activity using a fraction of the AcEO containing 1N2PE with 97.5 to 99% purity. This product was therefore applied to classic models of antinociceptive activity (abdominal contortions, hot plaque, and formalin) and antiedematogency (croton oil ear edema, paw edema by carrageenan or dextran), in addition to performing a theoretical study of functional density calculations. Regarding nociception, 1N2PE showed antinociceptive activity in a dose-dependent pattern (15, 25, and 50 mg/kg) when administered ip. The screening proceeded also revealed that it modulates only peripheral components of nociception, despite apparently involving opioid receptors in its mechanism of action (Lima et al., 2009). In inflammatory context, the results indicate the reduction of edema induced by croton oil, carrageenan, and dextran, with oral doses of 25 and 50 mg/kg (Vale et al., 2013). A possible mechanism related to these effects was pointed out by a conformational study conducted by Vale et al. (2013) who demonstrated that 1N2PE molecule had a favorable configuration for interaction with prostaglandin endoperoxide synthase.

Methyleugenol, the second major compound in AcEO, it also shows evidence of antinociceptive, anesthetic, and anti-inflammatory activity. According to Yano et al. (2006) research, its oral administration (10 mg/kg) reduces the second stage nociceptive response in formalin test. This effect was inhibited by bicuculline, a GABAa receptor antagonist, indicating that its activity would be related to the activation of these receptors. On the other hand, it did not promote any activity on cyclooxygenases 1 and 2. These findings seem to corroborate with Carlini et al. (1981) study, that attributed anesthetic activity to methyleugenol (200 and 300 mg/kg). Additionally, Choi et al. (2010) demonstrated a reduction in the expression of pro-inflammatory (IL-1B, IL-6, TNFα, and iNOS) and increased expression of anti-inflammatory (IL-10, TGF-B) mediators in rat and cell culture models of cerebral ischemia. In view of these results, there is still much to be done in elucidating mechanisms of its antinociceptive and anti-inflammatory properties. Also taking advantage of central nervous system activity evidences to better characterize its potential anti-neuroinflammatory effect.

Cardiovascular Activities

Cardiovascular effects of AcEO and its major components were elucidated through a partnership between researchers from the federal universities of Ceará and Pará (Brazil). The work developed by those groups initially demonstrated hypotension and bradycardia being promoted by intravenous (i.v.) injection of AcEO in normotensive rats, triggering in a dose-dependent pattern. According to the authors, such effects were linked, at least in part, to endothelial integrity factors, also identifying the participation of endothelial muscarinic receptors and stimulation of nitric oxide (NO) production, regulated by calcium flow (Lahlou et al., 2005). The same pattern was observed with i.v. administration of a concentrated fraction (98%) of 1N2PE (1, 3, 5, and 10 mg/kg) in normotensive anesthetized rats, indicating that 1N2PE was responsible for the vasorelaxant and bradycardic properties of AcEO (De Siqueira et al., 2010). According to the authors, this effect was a vago-vagal bradycardiac and depressor reflex generated by excitation of pulmonary afferent type C fibers. Also, 1N2PE has a direct effect on the vascular smooth muscle, promoting its relaxation. Thus, the authors demonstrated that the i.v. treatment with AcEO actively promoted vascular relaxation and consequent hypotension, not associated with the sympathetic tone (Lahlou et al., 2005; De Siqueira et al., 2010). In the next research stage, cardiovascular effects of AcEO and 1N2PE were tested in spontaneously hypertensive rats. Under these conditions, the i.v. administration of both AcEO (1, 5, 10, and 20 mg/kg) and 1N2PE (1, 3, 5, and 10 mg/kg) retained the same pattern of biphasic effect, composed of the vago-vagal bradycardic reflex (phase 1) and the direct vasodilatory action (phase 2; Figure 3) (Interaminense et al., 2010; Interaminense et al., 2013).

FIGURE 3
www.frontiersin.org

Figure 3 Proposed mechanism for the antihypertensive and bradycardic effects of Aniba canelilla essential oil and 1-nitro-2-phenylethane.

The biochemical pathways involved on those effects were investigated by Brito et al. (2013) who reported that 1N2PE would raise the levels of cyclic guanosine monophosphate (cGMP) in smooth muscle cells, suggesting a possible stimulation of guanylate cyclase (sGC). In addition, blocking the production of cyclic adenosine monophosphate (cAMP) or NO did not interfere with 1N2PE effects. Such evidence reveals the potential of 1N2PE for the treatment of cardiovascular diseases, such as systemic arterial hypertension and pulmonary arterial hypertension, and cerebrovascular diseases, such as stroke.

Neuropharmacological Activities

Despite the references of A. canelilla tea traditional use for the treatment of central nervous system-related conditions, such as Alzheimer's disease and depression, in addition to indication as calming (Rodrigues and Carlini, 2006; Madaleno, 2011; Almeida et al., 2013; Bitencourt et al., 2014; Santos et al., 2016), no studies were identified that explored such properties in this specie.

However, studies on the neuropharmacological properties of the two major constituents of AcEO, 1N2PE and methyleugenol, have been identified. 1N2PE, isolated (93% pure) from Dennettia tripetala G. Baker EO, an African Annonaceae species, promoted hypnotic effect in doses between 100 and 400 mg/kg (ip) in mice, reducing sleep latency with potency higher than pentobarbitone sodium (50 mg/kg; ip) and diazepam (20 mg/kg; ip). It also promoted a dose-dependent increase in sleep time, reaching an effect equivalent to diazepam (standard drug) at 400 mg/kg. 1N2PE also promoted protection in the model of Pentylenetetrazol (PTZ)-induced convulsions in mice. At a dose of 20 mg/kg, 20% protection was observed, while at doses above 50 mg/kg, seizures were fully inhibited. Pretreatment with flumazenil (2 mg/kg; ip) blocked the protection provided by 1N2PE, indicating a likely involvement of γ-aminobutyric acid (GABA) pathways in its effect. Finally, evidence of an anxiolytic effect was also evaluated in the plus-maze model at doses between 5 and 20 mg/kg (ip) with equivalent potency to diazepam (20 mg/kg) (Oyemitan et al., 2013). Silva et al. (2014), in turn, demonstrated that 1N2PE, isolated from AcEO, is a strong acetylcholinesterase blocker, with potency equivalent to physostigmine. Its effect was related to the positioning of its nitro group next to the enzyme catalytic serine residue, forming a potent hydrogen bond with its hydroxyl group.

Methyleugenol, in turn, has been described as a central nervous system depressant, with anticonvulsant and anesthetic effects (Dallmeier Zelger et al., 1983; Sayyah et al., 2002). In this context Ding et al. (2014) demonstrates in cultured hippocampal neurons the agonist property of this substance on GABAa receptors. Considering the majority presence of these constituents in AcEO, they can be the basis of the traditional indications described as calming. However, there are still other properties to be investigated, such as the influence on neurodegeneration, memory, and depressive behaviors.

Other Biological Activities

In addition to the effects addressed above, A. canelilla and its constituents have also been investigated for its antibiotic properties. Giongo et al. (2017), described the trypanomicidal effect of AcEO from bark, 1N2PE, and methyleugenol in a culture of Trypanosoma evansi, suggesting that may be a viable alternative for the treatment of this protozoosis. Silva et al. (2009), in turn, demonstrated the leishmanicidal effect of AcEO and 1N2PE on Leishmania amazonensis.

Antifungal activity has also been described. Evaluating EOs, hydrolates, ethanolic extract, and hexane and dichloromethane fractions of plant leaves or branches in the culture of bacteria (Staphylococcus aureus and Pseudomonas aeruginosa), human pathogenic fungi (Candida albicans), and phytopathogens (Didymella bryoniae and Corynespora cassiicola), reported that only EOs promoted growth inhibition and exclusively against C. albicans and D. bryoniae. These antifungal properties have been attributed mainly to 1N2PE (Oger et al., 1994; Silva, 2012).

Potential for Aging-Related Diseases Treatment

The human aging process involves the progressive alteration of the cell repair and proliferation capacity, in addition to nuclear and mitochondrial DNA alterations, constituting a progressively favorable context for the development of diseases. Among the events related to this senescence process is the so-called inflammating, a state caused by the increase in the production/release of inflammatory mediators and oxidative stress, caused by the imbalance between the production of ROS and the body's antioxidant capacity. The studies in this area discuss the cause and consequence relationships between the aging process and these two mechanisms, however, agree on the principle that they are key factors in the genesis and evolution of aging-related diseases, among which stands out the cancer, diabetes, and cardiovascular, respiratory, and neurological diseases (Khansari et al., 2009; Zuo et al., 2019) (Figure 4).

FIGURE 4
www.frontiersin.org

Figure 4 Prospects for assessing the therapeutic potential of Aniba canelilla in aging-related diseases, based on current knowledge. *Needs to be confirmed in biological models.

In this context, A. canelilla has great potential, as it brings together a set of advantageous activities for the treatment of clinical conditions related to inflammation and oxidative stress. The reviewed studies demonstrate the ability of the plant derivatives to modulate the inflammatory process by inhibiting pro-inflammatory and inducing anti-inflammatory cytokines, preventing edema formation and leukocyte migration to the focus of aggression (Lima, 2008; Choi et al., 2010; Vale et al., 2013). Based on these findings, much can be explored concerning the diversity of inflammatory diseases that can be benefited by their actions. Therefore, it is necessary to expand the studies on such actions, exploring its influences on the cellular inflammatory response, diapedesis mechanisms, and intracellular signaling pathways. Studies about its antioxidant properties, as previously mentioned, were limited to chemical DPPH tests (Silva et al., 2007; Silva, 2012; Mesquita et al., 2014; Martins et al., 2016), so we consider essential studies on its effects on ROS production, pro (NOX, NOS, XO, etc.) and antioxidant (Catalase, GPx, SOD, etc.) enzymes activity and macromolecules oxidation (lipid peroxidation, protein carbonylation, nucleic acid damage, etc.).

Regarding cardiovascular diseases (CVD), which emerge worldwide as the main cause of death (WHO, 2018), significant cardio modulatory and vasorelaxant effects of AcEO and its major constituent have been reported, leading to a reduction in blood pressure in hypertensive rats, through vago-vagal response and sGC stimulation, with consequent increase in cGMP production (Interaminense et al., 2010; Interaminense et al., 2013). It is important, however, to advance in the search for these effects. Antioxidant and anti-inflammatory properties of the plant could also promote additional benefits, reducing vascular remodeling, endothelial dysfunction, and atherosclerosis, which are induced/aggravated by inflammation and oxidative stress (Garcia et al., 2017; Zuo et al., 2019).

In view of the combination of vascular, anti-inflammatory, and antioxidant properties, we consider it is interesting to study its effects on the outcome of ischemic strokes (Kim et al., 2016). This condition is marked by rapid and intense neuronal death by apoptosis in ischemic core. In penumbra area, neuron death is triggered by glutamatergic excitotoxicity and oxidative stress, in addition to an important neuroinflammatory event, with the development of microgliosis and astrogliosis, and the release of pro-inflammatory cytokines (Fontes-Junior et al., 2016).

In fact, the interaction between oxidative stress and inflammation has been widely explored, identifying the interfaces between these mechanisms, that is, the state of “inflamming” increases the ROS production, favoring oxidative stress, in the same way as oxidative stress promotes the activation of inflammatory pathways and together are involved in chronic and degenerative conditions (Reuter et al., 2010). In addition, based on the evidence of the A. canelilla constituents action on central nervous system and traditional indications of use for the treatment of neurodegenerative conditions, such as Alzheimer's disease (AD), and depression (Rodrigues and Carlini, 2006; Madaleno, 2011), we consider it as a possible research line to be explored. The anticholinesterase effect attributed to 1N2PE may justify, at least in part, the use of A. canelilla for AD treatment, but there are no studies about its benefits on memory or disease progression, topic which assemble multiple mechanisms and must be elucidated in future studies. On behavior and emotionality, evidence of anxiolytic activity was observed (Oyemitan et al., 2013), but no study has yet explored traditional indications for depression treatment, considered an inflammatory disease too, or the supposed stimulating effect.

Final Considerations

Studies on the aromatic species A. canelilla, popularly known as “Casca preciosa,” have ratified several of its traditional indications, showing its commercial and therapeutic potential, including antioxidant, antinociceptive, anti-inflammatory, anticholinesterase, anxiolytic, anticonvulsant, hypnotic, cardio modulatory, vasorelaxant, and antibiotic properties, through the application of its EO, extracts, and major constituents (1N2PE and Methyleugenol). However, it is necessary to advance in characterization of its mechanisms of action, pharmacokinetic, and clinical potential applications arising from each property. Special attention should also be paid to possible synergisms resulted from combined properties, such as antioxidant (needs to be confirmed in biological models), anti-inflammatory, and cardiovascular, which open new therapeutic possibilities on aging-related diseases, such as the treatment of cerebrovascular, neurobehavioral, and chronic degenerative diseases.

Author Contributions

The review was conceived and designed by EF-J, FS-J, and DL-M. Data collection were performed by FS-J, DL-M, FP, MB, LF, and LQ. Data were analyzed by EF-J, FS-J, DL-M, CM, and JM. Drafting of the manuscript: FS-J, DL-M, FP, MB, LF, and LQ. Critical revision of the manuscript: EF-J, CM, and JM. All authors revised and approved the final version of the manuscript.

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.

Acknowledgments

We thank to Universidade Federal do Pará (UFPA) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for the financial support for this project. Thanks to Mr. Valter Vinicius Silva Monteiro for his contribution to English review.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2020.00699/full#supplementary-material

Figure S1 | Graphical abstract.

References

Almeida, M. R., Fidelis, C. H. V., Barata, L. E. S., Poppi, R. J. (2013). Classification of Amazonian rosewood essential oil by Raman spectroscopy and PLS-DA with reliability estimation. Talanta 117, 305–311. doi: 10.1016/j.talanta.2013.09.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Almeida, M. R., Martinez, S. T., Pinto, A. C. (2017). Chemistry of natural products: Plants that witness histories. Rev. Virtual Quimica. 9, 1117–1153. doi: 10.21577/1984-6835.20170068

CrossRef Full Text | Google Scholar

Araújo, V. F., De Petry, A. C., Echeverria, R. M., Fernandes, E. C., Pastore, F. (2007). Plantas da Amazônia para Produção Cosmética: uma abordagem química - 60 espécies do extrativismo florestal não-madeireiro da Amazônia. Brasília, 244: Universidade de Brasilia.

Google Scholar

Awad, M. A., Aldosari, S. R., Ruhul Abid, M. (2018). Genetic Alterations in Oxidant and Anti-Oxidant Enzymes in the Vascular System. Front. Cardiovas. Med. 117. doi: 10.3389/fcvm.2018.00107

CrossRef Full Text | Google Scholar

Barbosa, T. D. M., Baitello, J. B., Moraes, P. L. R. (2012). A família Lauraceae Juss. no município de Santa Teresa, Espírito Santo. Bol. Mus. Biol. Mello Leitão 30, 5–178.

Google Scholar

Barbosa, P. C. S., Fernandes, K. S., Manhães, A. P., Carneiro, S. B., Sampaio, P., de, T. B., et al. (2017). New and sustainable essential oils obtained from the long-term explored cinnamomum-like Aniba canelilla. J. Appl. Res. Med. Aromatic Plants 5, 60–71. doi: 10.1016/j.jarmap.2016.11.002

CrossRef Full Text | Google Scholar

Barros, I. B., Bonfim, R., Friburgo, N. (2018). The inhibitory action of Aniba Canelilla (H.B.K.) Mez extracts on the corrosion of carbon steel in hydrochloric acid medium. Mater. Res. 21, 1–8. doi: 10.1590/1980-5373-mr-2017-0786

CrossRef Full Text | Google Scholar

Bitencourt, B. L. G., Lima, P. G. C., Barros, F. B. (2014). Comércio e uso de plantas e animais de importância mágico-religiosa e medicinal no mercado público do Guamá, Belém do Pará. Revista Faculdade Santo Agostinho. 11 (3), 96–158. doi: 10.12819/2014.11.3.5

CrossRef Full Text | Google Scholar

Bizzo, H. R., Ana Maria, C. H., Rezende, C. M. (2009). Óleos essenciais no brasil: aspectos gerais, desenvolvimento e perspectivas. Quimica Nova. 32, 588–594. doi: 10.1590/S0100-40422009000300005

CrossRef Full Text | Google Scholar

Boccardi, V. (2019). Population Ageing: The Need for a Care Revolution in a World 2.0. Geriatrics 4, 47. doi: 10.3390/geriatrics4030047

CrossRef Full Text | Google Scholar

Botsaris, A. S. (2007). Plants used traditionally to treat malaria in Brazil: the archives of Flora Medicinal. J. Ethnobiol. Ethnomed. 3 (18), 1–8. doi: 10.1186/1746-4269-3-18

PubMed Abstract | CrossRef Full Text | Google Scholar

Bourdy, G., DeWalt, S. J., Chávez de Michel, L. R., Roca, A., Deharo, E., Muñoz, V., et al. (2000). Medicinal plants uses of the Tacana, an Amazonian Bolivian ethnic group. J. Ethnopharmacol. 70, 87–109. doi: 10.1016/S0378-8741(99)00158-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Branch, L. C., Silva, M. F. (1983). Folk medicine in alter do Chão, Pará Brasil. Acta Amaz 13, 737797. doi: 10.1590/1809-4392135737

CrossRef Full Text | Google Scholar

Brito, T. S., Lima, F. J. B., Aragão, K. S., De Siqueira, R. J. B., Sousa, P. J. C., Maia, J. G. S., et al. (2013). The vasorelaxant effects of 1-nitro-2-phenylethane involve stimulation of the soluble guanylate cyclase-cGMP pathway. Biochem. Pharmacol. 85, 780–788. doi: 10.1016/j.bcp.2012.12.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Bubols, G. B., Vianna, D. R., Medina-Remón, A., Von Poser, G., Lamuela-Raventos, R. M., Eifler-Lima, V. L., et al. (2013). The antioxidant activity of coumarins and flavonoids, Mini-Rev. Med. Chem. 13, 318–334. doi: 10.2174/138955713804999775

CrossRef Full Text | Google Scholar

Burdock, G. A. (2005). Fenaroli´s Handbook of Flavor Ingredients, Sixth Edition. (New York: CRC Press). doi: 10.1201/9781439847503-c3

CrossRef Full Text | Google Scholar

Carlini, E. A., Dallmeier, K., Zelger, J. L. (1981). Methyleugenol as a Surgical Anesthetic in Rodents. Experientia 37, 37–38. doi: 10.1007/BF01990065

PubMed Abstract | CrossRef Full Text | Google Scholar

Choi, Y. K., Cho, G.-S., Hwang, S., Kim, B. W., Lim, J. H., Lee, J.-C., et al. (2010). Methyleugenol reduces cerebral ischemic injury by suppression of oxidative injury and inflammation. Free Radical Res. 44, 925–935. doi: 10.3109/10715762.2010.490837

CrossRef Full Text | Google Scholar

Costa, P. S. P. (2013). Estudo etnobotânico e farmacognóstico de plantas antimaláricas de uso popular na comunidade céu do Mapiá, Pauini- AM [masters dissertation]. [Manaus] Universidade Federal do Amazonas, Faculdade de Ciências Farmacêuticas. Available in: https://tede.ufam.edu.br/handle/tede/5324

Google Scholar

Custódio, D. L., Veiga Junior, V. F. (2014). Lauraceae alkaloids. RCS Adv. 4, 21864–21890. doi: 10.1039/C4RA01904K

CrossRef Full Text | Google Scholar

Da Silva, J. K. R., Sousa, P. J. C., Andrade, E. H. A., Maia, J. G. S. (2007). Antioxidant capacity and cytotoxicity of essential oil and methanol extract of Aniba canelilla (H.B.K.) Mez. J. Agric. Food Chem. 55, 9422–9426. doi: 10.1021/jf071928e

PubMed Abstract | CrossRef Full Text | Google Scholar

Dallmeier Zelger, K. R., Zelger, J. L., Carlini, E. A. (1983). New anticonvulsants derived from 4-allyl-2-methoxyphenol (Eugenol): comparison with common antiepileptics in mice. Pharmacology 27, 40–49. doi: 10.1159/000137828

PubMed Abstract | CrossRef Full Text | Google Scholar

De Almeida, L. S., Gama, J. R. V., Oliveira, F., de, A., Ferreira, M. S. G., De Menezes, A. J. E. A., et al. (2013). Uso de Espécies Da Flora Na Comunidade Rural Santo Antônio, BR-163, Amazônia Brasileira. Floresta e Ambiente 20, 435–446. doi: 10.4322/floram.2013.044

CrossRef Full Text | Google Scholar

De Filipps, R. A., Maina, S. L., Crepin, J. (2004). Medicinal plants of the Guianas (Guyana, Surinam, French Guiana) Washington, D.C.: Dept. of Botany, National Museum of Natural History, Smithsonian Institution.

Google Scholar

De Siqueira, R. J. B., Macedo, F. I. B., Interaminense, L., de, F. L., Duarte, G. P., Magalhães, P. J. C., et al. (2010). 1-Nitro-2-phenylethane, the main constituent of the essential oil of Aniba canelilla, elicits a vago-vagal bradycardiac and depressor reflex in normotensive rats. Eur. J. Pharmacol. 638 (13), 90–98. doi: 10.1016/j.ejphar.2010.03.060

PubMed Abstract | CrossRef Full Text | Google Scholar

Deharo, E., Bourdy, G., Quenevo, C., Muñoz, V., Ruiz, G., Sauvain, M. (2001). A search for natural bioactive compounds in Bolivia through a multidisciplinary approach. Part V. Evaluation of the antimalarial activity of plants used by the Tacana Indians. J. Ethnopharmacol. 77, 91–98. doi: 10.1016/S0378-8741(01)00270-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Ding, J., Huang, C., Peng, Z., Xie, Y., Deng, S., Nie, Y. Z., et al. (2014). Electrophysiological characterization of methyleugenol: A novel agonist of GABA(A) receptors. ACS Chem. Neurosci. 5, 803–811. doi: 10.1021/cn500022e

PubMed Abstract | CrossRef Full Text | Google Scholar

Elizabetsky, E., Castilhos, Z. C. (1990). Plants Used as Analgesics by Amazonian Caboclos as a Basis for Selecting Plants for Investigation. Int. J. Crude Drug Res. 28 (4), 309–320. doi: 10.3109/13880209009082838

CrossRef Full Text | Google Scholar

Farias, A. B., Fernandes, F. S., Santos, R. A., Souza, E. S., Souza, J. V. B. (2017). Estudo fitoquímico e análise de fotoproteção dos extratos eóleos essenciais de aniba canelilla (H.B.K) Mez. J. Engr. Exact Sci. 3 (4), 0614–0620. doi: 10.18540/24469416030420170614

CrossRef Full Text | Google Scholar

Figueiredo, A. C., Barroso, J. G., Pedro, L. G., Scheffer, J. J. C. (2008). Factors affecting secondary metabolite production in plants: volatile components and essential oils. Flavour Frag J. 23 (4), 213226. doi: 10.1002/ffj.1875

CrossRef Full Text | Google Scholar

Fontes-Júnior, E. A., Maia, C. S. F., Fernandes, L. M. P., Gomes-Leal, W., Costa-Malaquias, A., Lima, R. R., et al. (2016). Chronic Alcohol Intoxication and Cortical Ischemia: Study of Their Comorbidity and the Protective Effects of Minocycline. Oxid. Med. Cell. Longevity 2016, 110. doi: 10.1155/2016/1341453

CrossRef Full Text | Google Scholar

Fournet, A., Barriosb, A. A., Muiiozb, V. (1994). Leishmanicidal and trypanocidal activities of Bolivian medicinal plants. J. Ethnopharm. 41, 19–37. doi: 10.1016/0378-8741(94)90054-X

CrossRef Full Text | Google Scholar

Francisco, J., Ortega, M. (1994). La etnobotánica en el descubrimiento del Río Apure (1648) Antropologica 85, 3–72.

Google Scholar

Franciscon, C. H., Miranda, I., de, S. (2018). Distribution and conservation of Aniba aubl. (Lauraceae Jussieu) species in brazil. Biota Neotropica. 18, 1–16. doi: 10.1590/1676-0611-BN-2017-0362

CrossRef Full Text | Google Scholar

García, N., Zazueta, C., Aguilera-Aguirre, L. (2017). Oxidative Stress and Inflammation in Cardiovascular Disease. Oxid. Med. Cell. Longevity 2017, 2–4. doi: 10.1155/2017/5853238

CrossRef Full Text | Google Scholar

Giongo, J. L., Vaucher, R. A., Da Silva, A. S., Oliveira, C. B., de Mattos, C. B., Baldissera, M. D., et al. (2017). Trypanocidal activity of the compounds present in Aniba canelilla oil against Trypanosoma evansi and its effects on viability of lymphocytes. Microbial. Pathogenesis 103, 13–18. doi: 10.1016/j.micpath.2016.12.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Gottlieb, O. R., Magalhães, M. T. (1959). Communications occurrence of 1-nitro-2-phenylethane in Ocotea pretiosa and Aniba canelilla. J. Org. Chem. 24, 2070–2071. doi: 10.1021/jo01094a050

CrossRef Full Text | Google Scholar

Gottlieb, O. R., Magalhães, M. T. (1960a). Essential oil of the bark and wood of Aniba canelilla. Perfum. Essent. Oil Rec. 51, 69–70.

Google Scholar

Gottlieb, O. R., Magalhães, M. T. (1960b). Physiological varieties of Ocotea pretiosa. II. Perfumer Essential Oil Record. 51, 18–21.

Google Scholar

Gottlieb, O. R. (1972). Chemosystematics of the Lauraceae. Phytochemistry 5, 1537–1570. doi: 10.1016/0031-9422(72)85001-5

CrossRef Full Text | Google Scholar

Guze, M., Luz, A. C., Paneque-Gálvez, J., Macía, M. J., Orta-Martínez, M., Pino, J., et al. (2014). Are Ecologically Important Tree Species the Most Useful? A Case Study from Indigenous People in the Bolivian Amazon. Econ. Bot. 20 (10), 1–15. doi: 10.1007/s12231-014-9257-8

CrossRef Full Text | Google Scholar

Hegde, K. S., Chandrashekhar, S., Rao, S. N., Manikkoth, S. (2014). Preclinical screening of phyllanthus amarus ethanolic extract for its analgesic and antimicrobial activity. Pharmacogn. Res. 7, 378–384. doi: 10.4103/0974-8490.159577

CrossRef Full Text | Google Scholar

Herrero-Jáuregui, C., García-Fernández, C., Sist, P. L. J., Casado, M. A. (2009). Conflict of use for multi-purpose tree species in the state of Pará, eastern Amazonia, Brazil. Biodivers. Conserv. 18 (4), 10191044–285. doi: 10.1007/s10531-008-9456-7

CrossRef Full Text | Google Scholar

Hu, Y.-Q., Ferguson, D. K., Li, C.-S., Xiao, Y.-P., Wang, Y.-F. (2007). Alseodaphne (Lauraceae) From the Pliocene of China and its paleoclimatic significance. Rev. Palaeobot. Palynol. 146, 277–285. doi: 10.1016/j.revpalbo.2007.06.002

CrossRef Full Text | Google Scholar

Interaminense, L. D. F. L., Siqueira, R. J., Xavier, F. E. (2010). Cardiovascular effects of 1-nitro-2-phenylethane, the main constituent of the essential oil of Aniba canelilla, in spontaneously hypertensive rats. Fund. Clin. Pharmacol. 25 (6), 661–669. doi: 10.1111/j.1472-8206.2010.00891.x

CrossRef Full Text | Google Scholar

Interaminense, L. D. F. L., Dos, Ramos-Alves, F. E., De Siqueira, R. J. B., Xavier, F. E., Duarte, G. P., et al. (2013). Vasorelaxant effects of 1-nitro-2-phenylethane, the main constituent of the essential oil of Aniba canelilla, in superior mesenteric arteries from spontaneously hypertensive rats. Eur. J. Pharmaceut. Sci. 48, 709–716. doi: 10.1016/j.ejps.2012.12.0337

CrossRef Full Text | Google Scholar

Khansari, N., Shakiba, Y., Mahmoudi, M. (2009). Chronic Inflammation and Oxidative Stress as a Major Cause of Age-Related Diseases and Cancer. Recent Patents Inflammation Allergy Drug Discovery 3, 73–80. doi: 10.2174/187221309787158371

CrossRef Full Text | Google Scholar

Kim, J., Fann, D. Y., Seet, R. C., Jo, D. G., Mattson, M. P., Arumugam, T. V. (2016). Phytochemicals in Ischemic Stroke. Neuromol. Med. 18, 283–305. doi: 10.1007/s12017-016-8403-0

CrossRef Full Text | Google Scholar

Kubitzki, K., Renner, S. (1982). Lauraceae l (Aniba and Aiouea): Flora Neotropica, Monograph Vol. 31 (New York: The New York Botanical Garden), 1–84.

Google Scholar

Kubitzki, K., Rohwer, J. G., Bittrich, V. (1993). The families and genera of vascular plants II (Berlin: Springer-Verlag Berlin Heidelberg).

Google Scholar

Lahlou, S., Figueiredo, A. F., Magalhães, P. J. C., Leal-Cardoso, J. H., Gloria, P. D. (2004). Cardiovascular effects of methyleugenol, a natural constituent present in many plant essential oils, in normotensive rats. Life Sci. 74, 2401–2412. doi: 10.1016/j.lfs.2003.09.063

PubMed Abstract | CrossRef Full Text | Google Scholar

Lahlou, S., Caldas Magalhães, P. J., Bezerra De Siqueira, R. J., Figueiredo, A. F., Leal Interaminense, L. F., Soares Maia, J. G., et al. (2005). Cardiovascular effects of the essential oil of Aniba canelilla bark in normotensive rats. J. Cardiovasc. Pharmacol. 46, 412–421. doi: 10.1097/01.fjc.0000175876.25296.f4

PubMed Abstract | CrossRef Full Text | Google Scholar

Liguori, I., Russo, G., Curcio, F., Bulli, G., Aran, L., Della-Morte, D., et al. (2018). Oxidative stress, aging, and diseases. Clin. Interv. Aging. 13, 757–772. doi: 10.2147/CIA.S158513

PubMed Abstract | CrossRef Full Text | Google Scholar

Lima, M., da, P., Silva, T. M. D., da Silva, J. D., Zoghbi, M., das, G. B., et al. (2004). Essential oil composition of leaf and fine stem of Aniba canelilla (Kunth) Mez from Manaus, Brazil. Acta Amazonica 34, 329–330. doi: 10.1590/s0044-59672004000200019

CrossRef Full Text | Google Scholar

Lima, A. B., Santana, M. B., Cardoso, A. S., Silva, J. K. R., Maia, J. G. S., Carvalho, J. C. T., et al. (2009). Antinociceptive activity of 1-nitro-2-phenylethane, the main component of Aniba canelilla essential oil. Phytomedicine 16, 555–559. doi: 10.1016/j.phymed.2008.10.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Lima, A. B. (2008). Estudo da ação antinociceptiva e antiinflamatória do 1-nitro-2-feniletano, principal constituinte da Aniba canelilla. [dissertação/dissertação de mestrado]. Belém (PA): Universidade Federal do Pará.

Google Scholar

Lima, P. G. C., Coelho-Ferreira, M., Oliveira, R. (2011). Plantas medicinais em feiras e mercados públicos do Distrito Florestal Sustentável da BR-163, estado do Pará, BrasilActa Bot. Bras. 25(2), 422–434. doi: 10.1590/S0102-33062011000200018

CrossRef Full Text | Google Scholar

Lorenzi, H., Matos, F. J. A. (2008). Medicinal Plants in Brazil: Native and Exotic (Nova Odessa, Brazil: Publisher Plantarum Institute).

Google Scholar

Lupe, F. A. (2007). Estudo da composição química de óleos essenciais de plantas aromáticas da Amazônia [dissertação/dissertação de mestrad] [Campinas (SP)]: Universidade Estadual de Campinas, Instituto de Química.). http://repositorio.unicamp.br/jspui/handle/REPOSIP/248371

Google Scholar

Luziatelli, G., Sorensen, M., Theilade, I., Molgaard, P. (2010). Asháninka medicinal plants: a case study from the native community of Bajo Quimiriki, Junín, Peru. J. Ethnobiol. Ethnomed. 6 (21), 1–23. doi: 10.1186/1746-4269-6-21

PubMed Abstract | CrossRef Full Text | Google Scholar

Madaleno, I. M. (2011). Plantas da medicina popular de São Luís, Brasil. Boletim Do Museu Paraense Emílio Goeldi. Ciências Humanas. 6, 273–286. doi: 10.1590/s1981-81222011000200002

CrossRef Full Text | Google Scholar

Maia, O. G. S., Andrade, L. H. A. (2009). Database of the amazon aromatic plants and their essential oils. Quimica Nova. 32, 595–622. doi: 10.1590/S0100-40422009000300006

CrossRef Full Text | Google Scholar

Maia, J. G., Zoghbi, M. G., Andrade, E. H. (2001). Plantas aromáticas na Amazônia e seus óleos essenciais (Belém: Série Adolpho Ducke, Museu Paraense Emílio Goeldi).

Google Scholar

Manhães, A. P., da Veiga-Júnior, V. F., Wiedemann, L. S. M., Fernandes, K. S., De Tarso Barbosa Sampaio, P. (2012). Biomass production and essential oil yield from leaves, fine stems and resprouts using pruning the crown of Aniba canelilla (H.B.K.) (Lauraceae) in the Central Amazon. Acta Amazonica. 42, 355–362. doi: 10.1590/s0044-59672012000300007

CrossRef Full Text | Google Scholar

Marques, C. A. (2001). Importância econômica da família Lauraceae Lindl. Floresta e Ambiente 8, 195–206.

Google Scholar

Martins, F. J., Caneschi, C. A., Vieira, J. L. F., Barbosa, W., Raposo, N. R. B. (2016). Antioxidant Activity and Potential Photoprotective from Amazon Native Flora Extracts. J. Photochem. Photobiol. B.: Biol. 161, 34–39. doi: 10.1016/j.jphotobiol.2016.05.012

CrossRef Full Text | Google Scholar

Matsuo, M., Kirkland, D. F., Underhill, E. W. (1972). 1-Nitro-2-phenylethane: a possible intermediate in the biosynthesis of benzyl glucosinolate. Phytochemistry 11, 697–701. doi: 10.1016/0031-9422(72)80034-7

CrossRef Full Text | Google Scholar

Mesquita, T. J. B., Silva, G. F., Albuquerque, P. M., Duvoisin-Júnior, S. (2014). Análise fitoquímica e determinação da capacidade antioxidante em extratos de Aniba canelilla (H.B.K.) Mez. Anais do XX Congresso Brasileiro de Engenharia Química. Florianópolis, Santa Catarina, Brasil, p. 8. doi: 10.5151/chemeng-cobeq2014-2075-15962-176825

CrossRef Full Text | Google Scholar

Mez, C. (1889). Lauraceae Americanae. Jahrb. Königl. Bot. Gart. Berlin 5, 1–556.

Google Scholar

Miliauskas, G., Van Beek, T. A., Venskutonis, P. R., Linssen, J. P. H., De Waard, P. (2004). Antioxidative activity of Geranium macrorrhizum. Eur. Food Res. Technol. 218, 253–261. doi: 10.1007/s00217-003-0836-7

CrossRef Full Text | Google Scholar

Mimica-Dukic, N., Bozin, B., Sokovic, M., Simin, N. (2004). Antimicrobial and Antioxidant Activities of Melissa officinalis L. (Lamiaceae) Essential Oil. J. Agric. Food Chem. 52, 2485–2489. doi: 10.1021/jf030698a

PubMed Abstract | CrossRef Full Text | Google Scholar

Moraes, L. L., Freitas, J. L., Filho, J. R. M., Silva, R. B., Borges, C. H., Santos, A. C. (2019). Ethno-knowledge of medicinal plants in a community in the eastern Amazon. Rev. Ciências Agrárias. 42, 565–573. doi: 10.19084/rca.15625

CrossRef Full Text | Google Scholar

Morais, A. A., Rezende, C. M. A. M., Bulow, M. V. V., Moura, J. C., Gottlieb, O. R., Marx, M. C., et al. (1972). Óleos essenciais de espécies do genero Aniba. Acta Amazônica 2, 41–44. doi: 10.1590/1809-43921972021041

CrossRef Full Text | Google Scholar

Mors, W. B., Rizzini, C. T., Pereira, N. A. (2000). Medicinal plants of Brazil (Michigan: Reference Publications, Inc).

Google Scholar

Naranjo, P., Kijoa, A., Giesbrecht, A. M., Gottlieb, O. R. (1981). Ocotea quixos, American cinnamon. J. Ethnopharmacol. 4, 233–236. doi: 10.1016/0378-8741(81)90038-6

PubMed Abstract | CrossRef Full Text | Google Scholar

OECD -, The Organization of Economic Cooperation Development (2001). The OECD Guideline No. 407 for Testing of Chemical - Repeated Dose Oral Toxicity - Rodent: 28-Day or 14-Day Study (Paris, France: OECD), 1–7.

Google Scholar

Oger, J. M., Duval, O., Richomme, P., Bruneton, J., Guinaudeau, H., Fournet, A. (1992). Noranicanine a new type of trioxygenated benzylisoquinoline isolation and synthesis. Heterocycles 34, 17.

Google Scholar

Oger, J. M., Fardeau, A., Richomme, P., Guinaudeau, H., Fournet, A. (1993). Nouveaux alcaloïdes isoquinoléiques isolés d'une Lauraceae bolivienne: Aniba canelilla H.B.K. Can. J. Chem. 71, 1128. doi: 10.1139/v93-149

CrossRef Full Text | Google Scholar

Oger, J. M., Richomme, P., Guinaudeau, H., Bouchara, J. P., Fournet, A. (1994). Aniba canelilla (H.B.k.) mez essential oil: Analysis of chemical constituents, fungistatic properties. J. Essential Oil Res. 6, 493–497. doi: 10.1080/10412905.1994.9698432

CrossRef Full Text | Google Scholar

Okogun, J. I., Ekong, D. E. U. (1969). Essential oil of Dennettia tripetala. Chem. Industry 8 (3), 669–671.

Google Scholar

Organismo Andino de Salud. (2014). Plantas medicinales de la subregión andina. Peru: Convenio Hipólito Unanue. Available in: https://www.orasconhu.org/sites/default/files/LIBRO%20PLANTAS%20MEDICINALES%20DE%20LA%20SUBREGI%C3%93N.pdf

Google Scholar

Oyemitan, I. A., Elusiyan, C. A., Akanmu, M. A., Olugbade, T. A. (2013). Hypnotic, anticonvulsant and anxiolytic effects of 1-nitro-2-phenylethane isolated from the essential oil of Dennettia tripetala in mice. Phytomedicine 20, 1315–1322. doi: 10.1016/j.phymed.2013.07.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Pinto, A. C. (1995). O Brasil dos viajantes e dos exploradores e a química de produtos naturais brasileira. Química Nova. 18, 608–615.

Google Scholar

Quignard, E. L. J., Pohlit, A. M., Nunomora, S. M., Pinto, A. C. S., Santos, E. V. M., Morais, S. K. R. (2003). Screening of plants found in amazonas state for lethality towards brine shrimp Acta Amaz. 33 (1), 93–104. doi: 10.1590/1809-4392200331104

CrossRef Full Text | Google Scholar

Quinet, A., Baitello, J. B., Moraes, P. L. R., de Assis, L., Alves, F. M. (2015). Lauraceae, in Lista de Espécies da Flora do Brasil, Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br/jabot/floradobrasil/FB143 [accessed in March 2019].

Google Scholar

Reuter, S., Gupta, S. C., Chaturvedi, M. M., Aggarwal, B. B. (2010). Oxidative stress, inflammation, and cancer: How are they linked?. Free Radical Biol. Med. 49 (11), 16031616. doi: 10.1016/j.freeradbiomed.2010.09.006

CrossRef Full Text | Google Scholar

Rianjanu, A., Roto, R., Julian, T., Hidayat, S., Kusumaatmaja, A., Suyono, E., et al. (2018). Polyacrylonitrile Nanofiber-Based Quartz Crystal Microbalance for Sensitive Detection of Safrole. Sensors 18 (4), 1150. doi: 10.3390/s18041150

CrossRef Full Text | Google Scholar

Ribeiro, J. E. L. S., Hopkins, M. J. G., Vicentini, A., Sothers, C. A., Costa, M. A. S., Brito, J. M., et al. (1999). Flora da Reserva Ducke: Guia de identificação das plantas vasculares de uma floresta de terra-firme na Amazônia Central (Manaus: INPA).

Google Scholar

Rodrigues, E., Carlini, E. A. (2006). Plants with possible psychoactive actions used by the Krahô Indians, Brazil. Revista Brasileira de Psiquiatria. 28 (4, 277–282. doi: 10.1590/S1516-44462006005000014

CrossRef Full Text | Google Scholar

Ruberto, G., Baratta, M. T. (2000). Antioxidant activity of selected essential oil components in two lipid model systems. Food Chem. 69, 167–174. doi: 10.1016/S0308-8146(99)00247-2

CrossRef Full Text | Google Scholar

Samy, R. P., Pushparaj, P. N., Gopalakrishnakone, P. (2008). A compilation of bioactive compounds from Ayurveda. Bioinformation 3, 100–110. doi: 10.6026/97320630003100

PubMed Abstract | CrossRef Full Text | Google Scholar

Sangwan, N. S., Farooqi, A. H. A., Shabih, F., Sangwan, R. S. (2001). Regulation of essential oil production in plants. Plant Growth Regulation 34, 3–21. doi: 10.1023/A:1013386921596

CrossRef Full Text | Google Scholar

Santos, J. X., Reis, A. R. S., Parry, S. M., Leão, F. M., Carvalho, J. C. (2016). Caracterização Etnobotânica de Essências Florestais com Fins Medicinais Utilizadas pela Etnia Xipaya, no Município de Altamira-PA. Biota Amazônia 6, 1–8. doi: 10.18561/2179-5746/biotaamazonia.v6n2p1-8

CrossRef Full Text | Google Scholar

Santos, E. R. Q. (2017). Óleos essenciais ricos em linalol (Aniba rosaeodora, A. parviflora e Aeollanthus suaveolens) na amazônia e seus efeitos neurocomportamentais em roedores. [dissertação/dissertação de mestrado]. Belém (PA): Universidade Federal do Pará.

Google Scholar

Sayyah, M., Valizadeh, J., Kamalinejad, M. (2002). Anticonvulsant activity of the leaf essential oil of Laurus nobilis against pentylenetetrazole- and maximal electroshock-induced seizures. Phytomedicine 9, 212–216. doi: 10.1078/0944-7113-00113

PubMed Abstract | CrossRef Full Text | Google Scholar

Serino, A., Salazar, G. (2019). Protective Role of Polyphenols against Vascular Inflammation, Aging and Cardiovascular Disease. Nutrients 11, 1–23. doi: 10.3390/nu11010053

CrossRef Full Text | Google Scholar

Silva, J. R., d, A., do Carmo, D. F. M., Reis, E. M., Machado, G. M. C., Leon, L. L., et al. (2009). Chemical and biological evaluation of essential oils with economic value from lauraceae species. J. Braz. Chem. Soc. 20, 1071–1076. doi: 10.1590/S0103-50532009000600011

CrossRef Full Text | Google Scholar

Silva, N. N. S., Silva, J. R. A., Alves, C. N., Andrade, E. H. A., Da Silva, J. K. R., Maia, J. G. S. (2014). Acetylcholinesterase inhibitory activity and molecular docking study of 1-nitro-2-phenylethane, the main constituent of Aniba canelilla essential oil. Chem. Biol. Drug Design 84, 192–198. doi: 10.1111/cbdd.12304

CrossRef Full Text | Google Scholar

Silva, G. F. (2012). Estudo do potencial biotecnológico de Aniba canelilla (H.B.K) Mez para obtenção de cosméticos. [dissertação/dissertação de mestrado]. Manaus (AM): Universidade do Estado do Amazonas.

Google Scholar

Silva, A. G., Lima, R. A., Silva, L. P., Souza, A. C. R. (2011). Uso, conservação e diversidade de plantas aromáticas, condimentares e medicinais para fins medicinais na comunidade Vila Princesa, Porto Velho-RO. Revista Pesquisa & Criação. [dissertação/dissertação de mestrado]. 10:2, 21–35. Avaliable in: http://www.periodicos.unir.br/index.php/propesq/article/view/409/448

Google Scholar

Silva, A. C. R., da, Lopes, P. M., Azevedo, M. M. B., de, Costa, D. C., Alviano, C. S., Alviano, D. S. (2012). Biological Activities of a-Pinene and β-Pinene Enantiomers. Molecules 17 (6), 63056316. doi: 10.3390/molecules17066305

CrossRef Full Text | Google Scholar

Sipe, H. J., Lardinois, O. M., Mason, R. P. (2014). Free Radical Metabolism of Methyleugenol and Related Compounds. Chem. Res. Toxicol. 27 (4), 483489. doi: 10.1021/tx400256b

CrossRef Full Text | Google Scholar

Sousa, P. J. C., Araujo, J. S., Pereira, L. L. S., Modro, M. N. R., Maia, J. G. S., Araujo, M. T. F., et al. (2009). Phytochemical and toxicological evaluations of the essential oil from the bark of aniba canellila (h.B.K.) Mez. J. Essential Oil Res. 21, 381–384. doi: 10.1080/10412905.2009.9700197

CrossRef Full Text | Google Scholar

Sousa, D. P. (2011). Analgesic-like Activity of Essential Oils Constituents. Molecules 16, 2233–2252. doi: 10.3390/molecules16032233

PubMed Abstract | CrossRef Full Text | Google Scholar

Sugimoto, M., de Jesus Amazonas da Silva, M., Froede Brito, L., dos Santos Borges, R., Amaral, F., de Araujo Boleti, A., et al. (2017). Anti-Inflammatory Potential of 1-Nitro-2-Phenylethylene. Molecules 22 (11), 1977. doi: 10.3390/molecules22111977

CrossRef Full Text | Google Scholar

Taveira, F. S. N., Lima, W. N., Andrade, E. H. A., Maia, J. G. S. (2003). Seasonal essential oil variation of Aniba canelilla. Biochem. Syst. Ecol. 31, 69–75. doi: 10.1016/S0305-1978(02)00088-1

CrossRef Full Text | Google Scholar

Taylor, L. (2005). Rosewood (Aniba canelilla, Aniba rosaeodora. In The Healing Power of Rainforest Herbs. A Guide to Understanding and Using Herbal Medicinals. Square One Publishers, Inc., New York. http://www.rain-tree.com/rosewood.htm [accessed March 2019].

Google Scholar

Thomas, E., Vandebroek, I. (2006). Guía de Plantas Medicinales: de los Yuracarés y Trinitarios del Territorio Indígena Parque Nacional Isiboro-Sécure, Bolivia. Bolívia: Imprenta Sirena.

Google Scholar

Tropicos.org (2019). Missouri Botanical Garden. http://www.tropicos.org/Name/40014791 [Acessed November 2019].

Google Scholar

Tsuchiya, H. (2017). Anesthetic Agents of Plant Origin: A Review of Phytochemicals with Anesthetic Activity. Molecules 22 (8), 1369. doi: 10.3390/molecules22081369

CrossRef Full Text | Google Scholar

Uttara, B., Singh, A. V., Zamboni, P., Mahajan, R. T. (2009). Oxidative Stress and Neurodegenerative Diseases: A Review of Upstream and Downstream Antioxidant Therapeutic Options. Curr. Neuropharmacol. 7, 65–74. doi: 10.2174/157015909787602823

PubMed Abstract | CrossRef Full Text | Google Scholar

Vale, J. K. L., Lima, A. B., Pinheiro, B. G., Cardoso, A. S., Silva, J. K. R., Maia, J. G. S., et al. (2013). Evaluation and theoretical study on the anti-inflammatory mechanism of 1-nitro-2-phenylethane. Planta Med. 79, 628–633. doi: 10.1055/s-0032-1328402

PubMed Abstract | CrossRef Full Text | Google Scholar

Van der Werff, H. (1991). A key to the genera of Lauraceae in the New World. Ann. Missouri Bot. Garden. 78, 377–387. doi: 10.2307/2399567

CrossRef Full Text | Google Scholar

Wittstock, U., Halkier, B. A. (2000). Cytochrome P450 CYP79A2 fromArabidopsis thalianaL. Catalyzes the Conversion of l-Phenylalanine to Phenylacetaldoxime in the Biosynthesis of Benzylglucosinolate. J. Biol. Chem. 275 (19), 1465914666. doi: 10.1074/jbc.275.19.14659

CrossRef Full Text | Google Scholar

World Health Organization (2018). Top 10 causes of death. Global Health Observatory. Avaliable in: https://www.who.int/gho/mortality_burden_disease/causes_death/top_10/en/

Google Scholar

Yano, S., Suzuki, Y., Yuzurihara, M., Kase, Y., Takeda, S., Watanabe, S., et al. (2006). Antinociceptive effect of methyleugenol on formalin-induced hyperalgesia in mice. Eur. J. Pharmacol. 553, 99–103. doi: 10.1016/j.ejphar.2006.09.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Zuo, L., Prather, E. R., Stetskiv, M., Garrison, D. E., Meade, J. R., Peace, T. I., et al. (2019). Inflammaging and Oxidative Stress in Human Diseases: From Molecular Mechanisms to Novel Treatments. Int. J. Mol. Sci. 20, 1–39. doi: 10.3390/ijms20184472

CrossRef Full Text | Google Scholar

Keywords: Aniba canelilla (Kunth) Mez, folk medicine, biological activities, toxicity, 1-nitro-2-phenylethane, methyleugenol

Citation: Souza-Junior FJC, Luz-Moraes D, Pereira FS, Barros MA, Fernandes LMP, Queiroz LY, Maia CF, Maia JGS and Fontes-Junior EA (2020) Aniba canelilla (Kunth) Mez (Lauraceae): A Review of Ethnobotany, Phytochemical, Antioxidant, Anti-Inflammatory, Cardiovascular, and Neurological Properties. Front. Pharmacol. 11:699. doi: 10.3389/fphar.2020.00699

Received: 02 December 2019; Accepted: 28 April 2020;
Published: 26 May 2020.

Edited by:

Yue Liu, Xiyuan Hospital, China

Reviewed by:

Maria A. Deli, Hungarian Academy of Sciences (MTA), Hungary
Yanfei Liu, Beijing University of Chinese Medicine, China

Copyright © 2020 Souza-Junior, Luz-Moraes, Pereira, Barros, Fernandes, Queiroz, Maia, Maia and Fontes-Junior. 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: Enéas A. Fontes-Junior, ZWZvbnRlc0B1ZnBhLmJy

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.