REVIEW article

Front. Pharmacol., 19 September 2023

Sec. Ethnopharmacology

Volume 14 - 2023 | https://doi.org/10.3389/fphar.2023.1247675

Hypericum sampsonii Hance: a review of its botany, traditional uses, phytochemistry, biological activity, and safety

  • 1. Guangdong Provincial Key Laboratory of Utilization and Conservation of Food and Medicinal Resources in Northern Region, Shaoguan University, Shaoguan, China

  • 2. College of Food Science and Technology, Shaoguan University, Shaoguan, China

  • 3. School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China

Abstract

Ethnopharmacological relevance: Hypericum sampsonii Hance, also known as Yuanbao Cao in Chinese, is a traditional medicinal herb from the Guttiferae family and has been widely used in China to treat various conditions, including dysentery, enteritis, mastitis, scrofula, and contusion.

Aim of the review: This review aims to provide a comprehensive overview of the botany, traditional uses, phytochemistry, biological activity and safety of H. sampsonii and to highlight its potential for medical application and drug development.

Materials and methods: We searched several databases, i.e., Web of Science, SciFinder, PubMed, CBM, CNKI, Google Scholar, etc., for relevant information on H. sampsonii. Additionally, we also consulted some books on Chinese medicine.

Results: To date, 227 secondary metabolites have been isolated from H. sampsonii, including polycyclic polyprenylated acylphloroglucinols (PPAPs), benzophenones, xanthones, flavonoids, naphthodianthrones, anthraquinones and aromatic compounds. These metabolites exhibit various biological activities such as anti-inflammatory, anti-tumor, anti-depressant, anti-oxidant, anti-viral and anti-bacterial effects. PPAPs are considered the main active metabolites with rich biological activities. Despite being known as rich source of PPAPs, the full extent of H. sampsonii biological activities, including their potential as PDE4 inhibitors, remained unclear. Since, previous studies have mainly been based on structural identification of metabolites in H. sampsonii, and efficacy evaluations of these metabolites based on clinical applications of H. sampsonii lack sufficient data. However, current evidence suggest that PPAPs are the most likely material basis for efficacy. From the limited information available so far, there is no evidence of potential safety issues and the safety data are limited.

Conclusion: Collectively, this review provides a comprehensive overview of the botany, traditional uses, phytochemistry, pharmacology, and safety of H. sampsonii, a valuable medicinal plant in China with various pharmacological activities. Based on pharmacological studies, H. sampsonii shows potential for treating gastrointestinal and gynecological disorders as well as traumatic injuries, which aligns with traditional medicinal use due to the presence of PPAPs, benzophenones, xanthones, and flavonoids. Therefore, further studies are needed to evaluate the pharmacological effects and elucidate the pharmacological mechanisms. In addition, pharmacological mechanisms and safety evaluation of PPAPs on animal models need to be clarified. Yet, further comprehensive studies are required to elucidate the phytochemical constituents, pharmacological mechanisms, structure-activity relationships, safety evaluation, and quality standards of this plant. Takentogether, this review highlights the potential of H. sampsonii for medical application and drug development.

1 Introduction

Plants have been used in traditional medicine for centuries to prevent and treat various diseases. Ethnomedicinal plants, which have clinical evidence of efficacy and safety, play an important role in drug discovery and development (Cragg and Pezzuto, 2016; Anand et al., 2019; Choudhari et al., 2020). The Hypericum genus (Guttiferae) boasts over 460 species that are distributed worldwide, with the exception of arctic and desert regions and most tropical lowlands. (Committee, 2007). Some species are widely used in official medicine throughout the world, such as Hypericum perforatum L. (St. John’s wort) (Stojanovic et al., 2013). However, some endemic species of Hypericum have traditionally been used as folk medicine or ethnomedicine in East Asia, particularly in China (Zhang et al., 2020). Hypericum sampsonii Hance (known as “Yuanbao Cao” in Chinese), which is used as a traditional medicine in south of Changjiang River, has been commonly used as a folk medicine with functions of traumatic bleeding, enteritis, dysentery, and acute mastitis (Gong, 2014; Xie et al., 2021).

Recent years have shown, growing interest of researchers in the chemical constituents and pharmacological effects of H. sampsonii. Previous chemical investigation of H. sampsonii reports a series of metabolites including polycyclic polyprenylated acylphloroglucinols (PPAPs), benzophenones, flavonoids, xanthones, naphthodianthrones, anthraquinones, and aromatic compounds (Xie et al., 2021). The previously reported literatures have revealed that H. sampsonii possesses multiple biological properties, including anti-inflammatory, antinociceptive, antitumor, antidepressant, antimicrobial, antiviral, and antioxidant activities (Tian, 2015; Xie et al., 2021). Accordingly, in the present srudy, we have attempted a pharmacological analysis of the whole plant H. sampsonii to understand the primary target of inflammation and to validate the ethnomedicine reports due to its numerous pharmacological activities and traditional claims of anti-inflammatory properties in the intestinal tract (Lin et al., 2022). However, biological activities and molecular mechanisms of constituents in H. sampsonii have not been fully explored, and a comprehensive and systematic review of this plant is lacking. The present study will not only provide motivation to the growing interest in recent years for a better understanding of the indication-discovery strategies but also assist the concept of drug repurposing in the treatment of many other related clinical conditions that may direct guide towords future research plan.

In this review, the botany, traditional uses, phytochemistry, pharmacological action, and safety of H. sampsonii have been summarized along with discussion over future direction and focus of H. sampsonii in the field of pharmacology.

2 Materials and methods

The relevant information was collected from various search engines: Web of Science, SciFinder, PubMed, CBM, CNKI, Google Scholar, etc. Other literature sources, i.e., classic books of Chinese herbal medicine were also screened to get the maximal information on this plant. The keywords used included H. sampsonii Hance, botany, phytochemistry, pharmacological activity, traditional uses, safety, and other related words. The plant name was also checked with World Flora Online (WFO (2023): Hypericum sampsonii Hance. Published on the Internet; http://www.worldfloraonline.org/taxon/wfo-0000728267. Accessed on: 04 February 2023).

3 Botany

According to World Flora Online, this name of H. sampsonii Hance (Figure 1) of Hypericaceae family has been accepted, with other four synonyms including Hypericum electrocarpum Maxim, H. electrocarpum f. parvifolium R. Keller, Hypericum esquirolii H. Lév, and Hypericum oshimaense R. Keller, in the genus Hypericum (family Hypericaceae). As a folk medicine, various vernacular names of H. sampsonii have been known in China, such as Hezhang Cao, Shangtianti, Dahuanhun, etc (Table 1).

FIGURE 1

TABLE 1

AreaNameRef.
JiangxiXiangsi, Dengtai, Shuanghehe, Duiye Cao, Daduiye Cao, Pai Cao, Duijing Cao, SanxuedanWu, 1963; Zhang et al. (2020)
GuangxiDaduiye Cao, Yebaozhi, Fanchuan Cao, Xiaohuangxin Cao, Baoxin Cao, Waxin Cao, Yangxingai (Miao people), Shanglianxialiu (Zhuang people), Mawu (Mulam people)Wu, 1991; Zhang et al. (2020)
FujianXiangsi, Dengtai, Shuanghehe, Duiye Cao, Yebaozhi, Dangguilian, Xiaolianqiao, Duilian, Ligenxiang, Danggui CaoZhang et al. (2020)
ZhejiangBaota Cao, Chuanxinjian, Lazhudengtai, Dengtai, Qingting Cao, Honghanlian, DayeyeyanziWu, 1963; Zhang et al. (2020)
GuizhouXiangsi, Dengtai, Shuanghehe, Duiye Cao, Duiyuelian, ShezhakouZhang et al. (2020)
HunanDaduiye Cao, Wangbuliuxing, Liujinu, Shaoxi Cao, Lanchang Cao, Yehanyan, Mangzi Cao, Shekaikou, Yangzi Cao, Yizi Cao, Jiaozhu CaoZhang et al. (2020)
Hunan Yaowu Zhi
《湖南药物志》
HubeiDaduiye Cao, Wangbuliuxing, Liujinu, Duiyue CaoZhang et al. (2020)
SichuanDaduiye Cao, Foxin Cao, Duidui CaoWu, 1963; Zhang et al. (2020)
JiangsuKongxin Cao, chuanxin CaoZhang et al. (2020)
GuangdongDaduiye CaoZhang et al. (2020)
AnhuiHuangyelianqiaoZhang et al. (2020)
YunnanFanchuan CaoZhang et al. (2020)

Vernacular names of H. sampsonii in China.

H. sampsonii, which look like gold ingot (Yuanbao in Chinese) by the connate perfoliate leaves, is a perennial herb with a height of approximately 0.2–0.8 m. The stem is erect and glabrous, with slender and short fibrous roots. The upright stem is cylindroid, and the upper part is branched. The shape of leaves is oblong to lanceolate or oblanceolate, (2–) 2.5–7 (8) cm long, (0.7–) 1–3.5 cm wide, and the apex is obtuse or rounded, sessile, with entire margins. Leaves are arranged in opposite and basally completely connate, green above and light green below with dense marginal black glands. The leaf midrib passes through the leaf apex, and both sides have four lateral veins oblique upward; the vein network is fine and sparse. Its inflorescences like corymbose, terminal, which form into the cylindrical panicle; the bracts and bractlets are linear-lanceolate or linear, 4 mm long, with an acuminate apex. The flowers are 6–10 (−15) mm in diameter, nearly oblate, and cup-shaped at the base; the buds are ovate with an obtuse apex. The pedicel is slender and 2–3 mm long; the sepals are oblong to oblong-spatulate or oblong-linear with 3–7 (–10) mm in length and 1–3 mm in width; the petals are light yellow, ovate, persistent, about 4–8 (−13) mm long and 1.5–4 (−7) mm wide, with marginal sessile or nearly sessile black glands. There are three stamens, each containing 10–14 stamens; the anther is light yellow with black glands. The ovary is ovoid to narrowly conical, three-celled, and about 3 mm long; the style is 3, about 2 mm long, separated from the base. The capsule is ovate with a length of 6–9 mm and covered with yellowish-brown glands; seeds are small long ovate, about 1 mm long with yellowish-brown. The fluorescence duration is from May to June and the fruiting period is from July to August. The whole plant is collected in summer or autumn, dried, and used for medicinal purposes (Editorial Committee of Flora of China, 1990; Xie, 2014; Li et al., 2019).

H. sampsonii not only favors a warm and humid environment but also tolerant to cold and drought. This plant is usually living on hillsides, roadsides, scrub, grassland, fields, and ditches, with an altitude of 0–1,200 m. It is commonly distributed in the south of the Yangtze River and Taiwan in China, and is also found in Japan, Northern Viet Nam, Eastern Myanmar, and Northeast India. Guangxi, Jiangsu, Zhejiang, and Sichuan are major provinces producing this plant (Editorial Committee of Flora of China, 1990).

4 Traditional uses

H. sampsonii has been traditionally used as a folk medicine for the treatment of gastrointestinal diseases and traumatic bleeding in China. The medicinal use of this plant was first recorded in the book of Ben Cao Cong Xin (本草从新) in Qing Dynasty, which proposed that it tastes acrid, is cold in nature, functions as nourishing Yin, and can be used to treat haematemesis and epistaxis (Wu, 1957). Textual Research on other monographs of Materia Medica, such as Bai Cao Jing and An Illustrated Book on Plants, records that the plant can be used for treating carbuncle due to toxins, traumatic injury, and deep-rooted breast carbuncles. It has the functions of clearing heat and detoxifying, relaxing tendons and activating collaterals, cooling blood and stopping bleeding. Clinically, H. sampsonii has been used to treat a variety of diseases, such as dysentery, enteritis, infantile fever, infantile convulsion, haematemesis, epistaxis, irregular menstruation, leucorrhea, traumatic bleeding, wounds, mastitis, burns, bedsores, and snakebites, etc (Editorial Board of Chinese Materia Medica, 1999; Xie, 2014; Xu, 2016; Vincent et al., 2021). According to the Gu Shang Zhong Cao Yao Shi Yong Tu Ce (Li et al., 2019), the fresh herb is often processed by pounding or grinding and used to treat traumatic injuries, gouty arthritis, and finger sores. In addition to external application, the whole plant is generally made into a decoction and taken orally for the treatment of rheumatic arthralgia, hemoptysis due to pulmonary trauma, stranguria due to hematuria, dysmenorrhea, and aphthous ulcers, etc. As a common folk medicine, the medicinal uses of H. sampsonii are documented in many local medicinal classics (Table 2). For example, Hunan Yaowu Zhi recorded that the whole plant of H. sampsonii can be used to treat diarrhea.

TABLE 2

CompositionaDosage formTraditional and clinical usesRef
元宝草(whole plant of Hypericum sampsonii Hance)UnrecordedTreat haematemesis and epistaxisBencao Congxin
《本草从新》
元宝草(whole plant of Hypericum sampsonii Hance)Decoction, and external useTreat irregular menstruation and relieve itchingFenlei Caoyaoxing
《分类草药性》
元宝草(whole plant of Hypericum sampsonii Hance)Decoction, and external useTreat diarrhea, thrush, nebula, burns, cuts, measles without adeqrate eruption, infantile rectocele, and lactation disturbanceHunan Yaowu Zhi
《湖南药物志》
元宝草(whole plant of Hypericum sampsonii Hance), 金银花(flower of Lonicera japonica Thunb.), 白头翁(roots of Pulsatilla chinensis (Bunge) Regel), 夏枯草(whole plant of Prunella vulgaris Linn., 酢浆草(whole plant of Oxalis corniculata L.), 油茶(leaves of Camellia oleifera Abel)External useTreat aphthosisHunan Yaowu Zhi
《湖南药物志》
元宝草(whole plant of Hypericum sampsonii Hance), 淫羊藿(leaves of Epimedium brevicornu Maxim), 油松(Pinus tabulaeformis Carr.).DecoctionTreat low back painHunan Yaowu Zhi
《湖南药物志》
元宝草(whole plant of Hypericum sampsonii Hance),车前子(seeds of Plantago asiatica L.), Gardenia jasminoides Ellis, Akebia quinata (Houtt.) DecneDecoctionTreat leucorrheaHunan Yaowu Zhi
《湖南药物志》
忍冬藤(stem of Lonicera japonica Thunb), 野菊花(flower of Dendranthema indicum (L.) Des Moul.),元宝草(whole plant of Hypericum sampsonii Hance), 冰片(borneol)External useTreat wounds festerHunan Yaowu Zhi
《湖南药物志》
元宝草(whole plant of Hypericum sampsonii Hance), 东方狗脊(root of Woodwardia orientalis Sw.), 四块瓦(leaves of Chloranthus serratus (Thunb.) Roem.), 槟榔(fruits of Areca catechu Linn.)External useTreat abdominal pain due to wormHunan Yaowu Zhi
《湖南药物志》
元宝草(whole plant of Hypericum sampsonii Hance), 蜂蜜(honey)DecoctionTreat erythral and leukal dysentery, and tenesmusZhejiang Minjian Caoyao
《浙江民间草药》
元宝草(whole plant of Hypericum sampsonii Hance), 大枣(fruits of Ziziphus jujuba Mill.)DecoctionTreat cough due to Yin dificiencyZhejiang Minjian Caoyao
《浙江民间草药》
元宝草(whole plant of Hypericum sampsonii Hance)External applicationTreat snake bites and finger soresZhejiang Minjian Caoyao
《浙江民间草药》
元宝草(whole plant of Hypericum sampsonii Hance), 水苏(whole plant of Stachys japonica Miq.), 灯笼草(whole plant of Clinopodium polycephalum (Vaniot) C. Y. Wu et Hsuan ex Hsu), 筋骨草(whole plant of Ajuga ciliata Bunge), 玄参(roots of Scrophularia ningpoensis Hemsl.)DecoctionTreat chronic pharyngitis and hoarsenessZhejiang Minjian Changyong Caoyao
《浙江民间常用草药》
元宝草(whole plant of Hypericum sampsonii Hance), 白酒(alcohol),黄酒(rice wine)Decoction, and external useTreat traumatic injuryJiangxi Minjian Caoyao
《江西民间草药》
元宝草(whole plant of Hypericum sampsonii Hance), 白酒(alcohol)DecoctionTreat breast carbuncleJiangxi Minjian Caoyao
《江西民间草药》
元宝草(whole plant of Hypericum sampsonii Hance), 商陆(roots of Phytolacca acinosa Roxb.), 白酒(alcohol)Steeping wineTreat irregular menstruationGuizhou Minjian Fangyaoji
《贵州民间方药集》
元宝草(whole plant of Hypericum sampsonii Hance), 马鞭草(whole plant of Verbena officinalis Linn.)DecoctionTreat lochiaGuizhou Minjian Fangyaoji
《贵州民间方药集》
元宝草(whole plant of Hypericum sampsonii Hance), 长春花(flowers of Catharanthus roseus (L.) G. Don.), 川芎(roots of Ligusticum chuanxiong Hort.)Steeping wineTreat menstrual painGuizhou Minjian Fangyaoji
《贵州民间方药集》
元宝草(whole plant of Hypericum sampsonii Hance), 猪肉(pork)DecoctionTreat hemoptysisQuanzhou Bencao
《泉州本草》
长春花(flowers of Catharanthus roseus (L.) G. Don.), 益母草(whole plant of Leonurus japonicus Houtt.), 元宝草(whole plant of Hypericum sampsonii Hance), dry winesDecoctionTreat irregular menstruationChongqing Caoyao
《重庆草药》
大叶仙茅(roots of Curculigo capitulata Kuntze), 萱草根(roots of Hemerocallis fulva (L.) L.), 女贞子(fruits of Ligustrum lucidum W.T.Aiton), 异叶鼠李(roots of Rhamnus heterophylla Oliv.), 茺蔚子(seeds of Leonurus japonicus Houtt.), 元宝草(whole plant of Hypericum sampsonii Hance), 金樱子(seeds of Rosa laevigata Michx.), 大枣(fruits of Ziziphus jujuba Mill.)Stewing with chickenTreat irregular menstruationSichuan Zhongyao Zhi
《四川中药志》
四叶葎(whole plant of Galium bungei Steud.), 地锦草(whole plant of Euphorbia humifusa Willd.), 元宝草(whole plant of Hypericum sampsonii Hance), 地耳草(whole plant of Hypericum japonicum Thunb.), 马鞭草(whole plant of Verbena officinalis Linn.), 酢浆草(whole plant of Oxalis corniculata L.), 鹅不食草(Centipeda minima (L.) A.Braun & Asch.), 天胡荽(Hydrocotyle sibthorpioides Lam.), 飞扬草(whole plant of Euphorbia hirta Linn.), 半边莲(whole plant of Lobelia chinensis Lour.), 白花蛇舌草(whole plant of Hedyotis diffusa Willd.), 墨旱莲(whole plant of Eclipta prostrata (L.) L.), 鬼针草(whole plant of Bidens Pilosa L.), 野甘草(Scoparia dulcis L.), 海金沙(Lygodium japonicum (Thunb.) Sw.)Powder, decoction, or external applicationTreat soft tissue contusion, traumatic fracture, postoperative infection, snake bites, burns, appendicitis, nephritis, hepatitis, cholecystitis, pancreatitis, etcYu (1995)
柴胡(roots of Bupleurum chinense DC.), 白芍(roots of Paeonia lactiflora Pall.), 郁金(roots of Curcuma aromatica Salisb.), 枳实(fruits of Citrus aurantium L.), 白术(roots of Atractylodes macrocephala Koidz.), 茯苓(Poria cocos (Schw.)Wolf), 陈皮(seedcase of Citrus reticulata Blanco), 元宝草(whole plant of Hypericum sampsonii Hance), 贯叶连翘(leaves of Hypericum perforatum L.), 甘草(roots of Glycyrrhiza uralensis Fisch.)DecoctionTreat generalized anxiety disorder due to Liver-qi stagnationChen (2020)
柴胡(roots of Bupleurum chinense DC.), 贯叶连翘(leaves of Hypericum perforatum L.), 元宝草(whole plant of Hypericum sampsonii Hance), 当归(roots of Angelica sinensis (Oliv.) Diels), 白芍(roots of Paeonia lactiflora Pall.), 川芎(roots of Ligusticum chuanxiong Hort.), 茯苓(Poria cocos (Schw.)Wolf), 白术(roots of Atractylodes macrocephala Koidz.), 酸枣仁(fruits of Ziziphus jujuba var. spinosa (Bunge) Hu ex H.F.Chow), 知母(roots of Anermarrhena asphodeloides Bunge), 远志(roots of Polygala tenuifolia Willd.), 甘草(roots of Glycyrrhiza uralensis Fisch.).DecoctionTreat Generalized Anxiety DisorderLin (2018)

The traditional and clinical uses of H. sampsonii in China.

a

All of the plant names have been checked with “World Flora Online” (www.worldfloraonline.org) mentioning the data of accessing that website.

H. sampsonii was also widely utilized as ethnomedicine by national minorities in China. In Sandu Shui Autonomous County located in the south of Guizhou Province of China, the botanical drug was commonly used as the liquor fermentation starter by the Shui people. Besides the edible value, this wild plant also possesses a wide range of medicinal values and can be used to treat irregular menstruation, leucorrhea, dysentery, and fever (Hong et al., 2015b). Furthermore, it was often used as an herbal tea to treat gynaecopathia by the Yao minority (Jin et al., 2018). H. sampsonii was also the medicinal plant traditionally used by Mulam people in Guangxi Province. It was mainly used to treat internal hemorrhage, abnormal menstruation, dysmenorrhea, and bleeding wound (Hu et al., 2020). According to the ethnobotanical data collected from the Maonan minority, H. sampsonii was used for the treatment of traumatic injury, pain, indigestion, chest congestion, and acute icteric hepatitis (Hong et al., 2015a; Xiang et al., 2018).

Additionally, the whole plant of H. sampsonii is most frequently reported as a traditional treatment for various diseases. Commonly, two processing methods (internal use and external application) are used before clinical use or self-medication. Firstly, it is processed by removing impurities and non-medicinal parts together with auxiliary materials such as honey and alcohol. Subsequently, the dried or fresh herb is often made as a decoction for oral administration to treat various diseases. Furthermore, in the second step, the dried herb can be ground or freshly pounded, and applied to the affected area for external use.

5 Phytochemistry

Chemical investigation of the Hypericum species include a series of phloroglucinol derivatives, naphthodianthrones, xanthones, flavonoids, and other phenols and terpenoids (Zhang et al., 2020). Of these, phloroglucinol derivatives are the main secondary metabolites. H. sampsonii is a rich source of natural products with diverse chemical structures. To date, a total of 223 metabolites including polycyclic polyprenylated acylphloroglucinols (PPAPs), benzophenones, xanthones, flavonoids, bisanthraquinones, and anthraquinones have been separated and identified from H. sampsonii (Supplementary Figure S10).

5.1 Polycyclic polyprenylated acylphloroglucinols (PPAPs)

Phloroglucinols, a type of natural products showing strong oxidizing properties, variable stereochemical structures, and a wide range of pharmacological activities, are decorated with isoprenyl and hydroxyl groups which are substituted at multiple positions on the benzene ring or fused together to form a ring (Xiao and Mu, 2007). PPAPs were highly oxygenated acylphloroglucinol derivatives which decorated with complicated side chains. In the past decades, PPAPs have received extensive attention due to their considerable structural diversity and remarkable biological activities (Yang et al., 2018). Biogenetically, all PPAPs which are derived from a common biosynthetic pathway via different cyclizations of the less complex monocyclic polyprenylated acylphloroglucinols, are generated via three main biosynthetic pathways (Yang et al., 2018). Interestingly, this special class of phloroglucinols has been exclusively isolated from the plants of family Guttiferae (Clusiaceae) and mainly from the genera Hypericum and Garcinia. Up to December 2022, 116 PPAPs comprise the major family of metabolites identified from H. sampsonii (Tables 3, 4, 5). All of the PPAP profiles are generated via three major biosynthetic pathways and may be divided into three groups according to their different scaffolds. Group I are the bicyclic polyprenylated acylphloroglucinols (BPAPs) with major bicyclo [3.3.1]nonane-2,4,9-trione core and related seco-BPAPs. Group II include the caged PPAPs with adamantane (tricyclo [3.3.1.1]decane) and homoadamantane (tricyclo [4.3.1.1]undecane) skeletons. Group III contain other biosynthetically related derivatives which derived from direct cyclizations of monocyclic polyprenylated acylphloroglucinols (MPAPs).

TABLE 3

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
17-EpiclusianoneC33H42O4502.70RootXiao et al. (2007)
2Attenuatumione CC38H50O5586.81Aerial partZhu et al. (2015)
3Hyperattenin CC38H50O5586.81Aerial partZhang et al. (2016)
4Hyperattenin EC33H43O5519.70Aerial part(Tian, 2015)]
5Hyperforatin FC33H48O5524.74Whole plantChen et al. (2020)
6HyperforinC35H52O4536.80Aerial partZheng et al. (2003)
7Hyperibone AC33H42O5518.69Aerial partZhang et al. (2016)
8Hyperibone IC33H42O5518.69Aerial partTian (2015)
9Hypersampsone FC38H48O4568.80Aerial partLin and Wu (2003)
10Hypersampsone HC38H50O4570.80FruitZeng et al. (2009)
11Hypersampsone KC38H50O4570.80FruitZeng et al. (2012)
12Otogirinin DC38H50O5586.81Aerial partZhu et al. (2015)
13Otogirinin EC38H50O6602.81Aerial partTian (2015)
14Hyperisampsin HC35H42O6558.72Aerial partZhu et al. (2017b)
15Hyperisampsin IC35H42O6558.72Aerial partZhu et al. (2017b)
16Hyperisampsin JC38H50O7618.81Aerial partZhu et al. (2017b)
17Hyperisampsin KC38H50O8634.81Aerial partZhu et al. (2017b)
18Hyperisampsin LC38H50O8634.81Aerial partZhu et al. (2017b)
19Hyperisampsin MC38H50O7618.81Aerial partZhu et al. (2017b)
20Hypersampsone RTC30H36O4460.61Aerial partTian et al. (2014b)
21Hypersampsone RCC32H42O3474.68Aerial partChen et al. (2014)
22Hypersampsone STC38H50O5586.81Aerial partTian et al. (2016)
23Hypersampsone TC33H42O4502.70Aerial partTian et al. (2016)
24Hypersampsone UC33H42O5518.69Aerial partTian et al. (2016)
25Hypersampsone VC33H44O7552.71Aerial partTian et al. (2016)
26Hypersampsone WC33H44O7552.71Aerial partTian et al. (2016)
27Sampsonione KC38H50O5586.81Aerial partHu and Sim (2000)
28Sampsonione LC33H42O5518.69Aerial partHu and Sim (2000)
29Sampsonione MC38H50O5586.81Aerial partHu and Sim (2000)
30Sampsonione NC33H42O5518.69RootXiao et al. (2007)
31Sampsonione OC33H42O5518.69RootXiao et al. (2007)
32Sampsonione PC33H42O5518.69RootXiao et al. (2007),Huang et al. (2022)

Bicyclic Polyprenylated Acylphloroglucinols (BPAPs) isolated from H. sampsonii.

T and C These compound names are distinguished by the initials of authors because of their different structures while identical names.

TABLE 4

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
3328,29-Epoxyplukenetione AC33H40O5516.68Aerial partZhu et al. (2014)
34Attenuatumione DC38H50O5586.81Aerial partZhang et al. (2016)
35Cowabenzophenone BC35H44O5544.73Aerial partZhang et al. (2016)
36Dioxasampsone AC33H42O6534.69Aerial partTian et al. (2014b)
37Dioxasampsone BC33H42O7550.69Aerial partTian et al. (2014b)
38Hyperattenin GC35H42O5542.72Aerial partZhang et al. (2016)
39Hyperattenin IC38H50O6602.81Aerial partZhang et al. (2016)
40Hypercohone AC33H42O5518.69Aerial partChen et al. (2014)
41Hyperibone KC33H40O4500.70Aerial partChen et al. (2014)
42Hypericumone AC32H40O4488.67Aerial partHuang et al. (2020)
43Hyperisampsin AC38H50O6602.81Aerial partZhu et al. (2015)
44Hyperisampsin BC38H50O5586.81Aerial partZhu et al. (2015)
45Hyperisampsin CC38H48O5584.80Aerial partZhu et al. (2015)
46Hyperisampsin DC38H50O7618.81Aerial partZhu et al. (2015)
47Hyperisampsin EC33H40O5516.68Aerial partZhu et al. (2015)
48Hyperisampsin FC33H42O6534.69Aerial partZhu et al. (2015)
49Hyperisampsin GC38H48O5584.80Aerial partZhu et al. (2015)
50Hyperisampsin NC38H50O7618.81Aerial partZhu et al. (2017b)
51Hyperisampsin OC38H50O8634.81Aerial partZhu et al. (2017b)
52Hypersampsone AC35H50O4534.78Aerial partLin and Wu (2003)
53Hypersampsone BC35H52O4536.80Aerial partLin and Wu (2003)
54Hypersampsone CC32H46O4494.72Aerial partLin and Wu (2003)
55Hypersampsone DC38H50O4570.80Aerial partLin and Wu (2003)
56Hypersampsone EC38H50O4570.80Aerial partLin and Wu (2003)
57Hypersampsone GC38H50O4570.80FruitZeng et al. (2009)
58Hypersampsone IC35H44O4528.73FruitZeng et al. (2012a)
59Hypersampsone JC38H48O4568.80FruitZeng et al. (2012a)
60Hypersampsone LC38H50O4570.80FruitZeng et al. (2012a)
61Hypersampsone MC30H36O4460.61Aerial partTian et al. (2014c)
62Hypersampsone NC30H36O6492.61Aerial partTian et al. (2014a)
63Hypersampsone OC33H40O5516.68Aerial partTian et al. (2014a)
64Hypersampsone PC30H36O4460.61Aerial partTian et al. (2014a)
65Hypersampsone QC33H42O5518.69Aerial partTian et al. (2014a)
66Hypersampsone SCC32H46O4494.72Aerial partChen et al. (2014)
67Hypersampsone XC33H40O4500.70Aerial partTian et al. (2017b)
68Hypersampsonone AC38H50O5586.81Aerial partZhang et al. (2016)
69Hypersampsonone BC35H44O6560.73Aerial partZhang et al. (2016)
70Hypersampsonone CC38H50O7618.81Aerial partZhang et al. (2016)
71Hypersampsonone DC39H52O6616.84Aerial partZhang et al. (2016)
72Hypersampsonone EC35H44O6560.73Aerial partZhang et al. (2016)
73Hypersampsonone FC38H50O6602.81Aerial partZhang et al. (2016)
74Hypersampsonone GC38H50O5586.81Aerial partZhang et al. (2016)
75Hyphenrone NC38H50O6602.81Aerial partZhang et al. (2016)
76Norsampsone EC29H42O4454.65Aerial partTian et al. (2017b)
77Otogirinin AC38H49O4569.81Aerial partHuang et al. (2020)
78Otogirinin BC38H50O7618.81Aerial partZhu et al. (2017b)
79Otogirinin CC38H50O5586.81Aerial partZhu et al. (2017b)
80Peroxysampsone AC33H42O8566.69RootXiao et al. (2010)
81Peroxysampsone BC33H42O7550.69RootXiao et al. (2010)
82Plukenetione BC33H42O5518.69Aerial partChen et al. (2014)
83Plukenetione AC33H40O4500.70Aerial partTian (2015)
84Plukenetione CC33H42O7550.69RootXiao et al. (2010)
85Sampsonione AC38H50O5586.81Aerial partHu and Sim (1998)
86Sampsonione BC33H42O5518.69Aerial partHu and Sim (1998)
87Sampsonione CC38H50O5586.81Aerial partHu and Sim (1999b)
88Sampsonione DC38H48O4568.80Aerial partHu and Sim (1999b)
89Sampsonione EC35H42O5542.72Aerial partHu and Sim (1999b)
90Sampsonione FC38H50O5586.81Aerial partHu and Sim (1999b)
91Sampsonione GC33H42O5518.69Aerial partHu and Sim (1999b)
92Sampsonione HC35H44O4528.73Aerial partHu and Sim (1999b)
93Sampsonione IC38H48O5584.80Aerial partHu and Sim (1999a)
94Sampsonione JC38H48O5584.80Aerial partHu and Sim (1999a)
95Sampsonione QC33H40O5516.68RootXiao et al. (2007)
96Sampsonione RC30H36O5476.61RootXiao et al. (2007)

Caged PPAPs isolated from H. sampsonii.

TABLE 5

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
97Hyperhexanone AC39H54O6618.86Aerial partZhu et al. (2016b)
98Hyperhexanone BC30H42O2434.66Aerial partZhu et al. (2016b)
99Hyperhexanone FC34H46O6550.74Aerial partZhang et al. (2021)
100Hypsampsone AC33H40O6532.68Aerial partZhang et al. (2021)
101Norhypersampsone AC20H24O3312.41Aerial partZhang et al. (2017)
102Norsampsone AC32H44O3476.70Aerial partTian et al. (2014c)
103Norsampsone BC32H44O3476.70Aerial partTian et al. (2014c)
104Norsampsone CC37H52O3544.82Aerial partTian et al. (2014c)
105Norsampsone DC37H52O3544.82Aerial partTian et al. (2014c)
106Hypericumone BC30H42O2434.66Aerial partHuang et al. (2020)
107Sampsone AC22H24O6384.43Aerial partXin et al. (2011b)
108Sampsonol AC33H42O7550.69Aerial partXin et al. (2012)
109Sampsonol BC33H42O7550.69Aerial partXin et al. (2012)
110Sampsonol CC29H34O5462.59Aerial partXin et al. (2012)
111Sampsonol DC29H34O6478.59Aerial partXin et al. (2012)
112Sampsonol EC27H38O5442.60Aerial partXin et al. (2012)
113Sampsonol FC26H36O5428.57Aerial partXin et al. (2012)
114Hypersampson AC37H50O4558.80Aerial partHuang et al. (2022)
115Hypersampson BC37H50O4558.80Aerial partHuang et al. (2022)
116Hypersampson CC37H50O4558.80Aerial partHuang et al. (2022)

Other PPAPs isolated from H. sampsonii.

5.1.1 Bicyclic polyprenylated acylphloroglucinols (BPAPs)

The bicyclic polyprenylated acylphloroglucinols (BPAPs) with major bicyclo [3.3.1] nonane-2,4,9-trione core and related seco-BPAPs (132, Table 3) include 32 BPAPs in which the acyl group is located at the C-1 or C-3 position. In 2000, BPAPs (Sampsoniones K-M, 27-29) were first discovered in the ethanolic extract of the aerial parts of H. sampsonii (Hu and Sim, 2000). Since then, BPAPs have been increasingly explored from the roots, fruits, and aerial part of H. sampsonii.

5.1.2 Caged PPAPs with adamantane or homoadamantane skeletons

It is noteworthy that H. sampsonii is a rich source of caged PPAPs, and about 64 adamantane- and homoadamantane-type derivatives with adamantane (tricyclo [3.3.1.1]decane) and homoadamantane (tricyclo [4.3.1.1]undecane) (3396, Table 4) have also been isolated from this plant. As early as 1998, Hu and Sim isolated two caged PPAPs (sampsoniones A and B, 85–86) from the aerial parts of H. sampsonii (Hu and Sim, 1998). Subsequently, they discovered sampsoniones C-J (87–94) (Hu and Sim, 1999a; b, 2000). A few years later, sampsoniones Q-R (95–96) were isolated from the root of H. sampsonii (Xiao et al., 2007). Since then, a large number of studies of caged PPAPs which were isolated from H. sampsonii have been reported, primarily focusing on its structure diversity with an unprecedented carbon skeleton. The tetracyclo [6.3.1.1(3,10).0(3,7)]tridecane skeletons and biogenetically related congeners, such as 28,29-Epoxyplukenetione A (33) (Zhu et al., 2014), hyperisampsins A-G (43–49) (Zhu et al., 2014), hyperisampsins N (50), and hyperisampsins O (51) (Zhu et al., 2017a), hypersampsones A-E (52–56) (Lin and Wu, 2003), hypersampsones L-S (60–66) (Zeng et al., 2012b), and hypersampsonones A-G (68–74) (Zhang et al., 2016).

5.1.3 Other PPAPs

A total of 20 other PPAPs such as spirocyclic PPAPs with octahydrospiro-[cyclohexan-1,5′-indene] core and complicated PPAPs via intramolecular [4 + 2] cycloadditions from MPAPs (97-116, Table 5) have been isolated from H. sampsonii. In 2011, a novel prenylated aromatic lactone (sampsone A, 107) was isolated from the aerial parts of H. sampsonii (Xin et al., 2011). Soon afterwards, six new acylphloroglucinol derivatives, (sampsonols A-F, 108–113), were discovered from the aerial parts of H. sampsonii (Xin et al., 2012). In 2014, four new decarbonyl PPAPs, (norsampsones A-D, 102-105), were isolated from the 60% EtOH extract of the aerial parts of H. sampsonii (Tian et al., 2014c). Recently, three nor-polycyclic polyprenylated acylphloroglucinols with a tetracyclic 6/5/5/6 ring system, (Hypersampones A-C, 114-116), which showed a lipid-lowering activity, were isolated from H. sampsonii. (Huang et al., 2022).

5.2 Benzophenones

Natural benzophenone derivatives have attracted extensive attention due to their unique structures and extensive biological activities. In accordance with the literature, benzophenones, mainly including simple benzophenone derivatives (SBDS) and polyprenylated benzophenones (PPBS), may be the precursors of some xanthones (Kitanov and Nedialkov, 2001). Currently, there are 33 benzophenones isolated from H. sampsonii (Supplementary Figure S4; Table 6). Among them, two pairs of racemic PPBS, (±)-sampsonin A-B (117–120) were chirally separated from H. sampsonii (Tian et al., 2017a). In addition, seven benzophenone derivatives sampbenzophenones A-G (140–146) were isolated from the aerial parts of H. sampsonii (Zhu et al., 2016a).

TABLE 6

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
117(−)-Sampsonin AC28H32O4432.56Aerial partTian et al. (2017a)
118(−)-Sampsonin BC28H32O4432.56Aerial partTian et al. (2017a)
119(+)-Sampsonin AC28H32O4432.56Aerial partTian et al. (2017a)
120(+)-Sampsonin BC28H32O4432.56Aerial partTian et al. (2017a)
121(E)-3-(3,7-dimethylocta-2,6-dienyl)-2,4,6-trihydroxybenzophenoneC23H26O4366.46Aerial partZhang et al. (2017)
122(Z)-3-(3,7-dimethylocta-2,6-dienyl)-2,4,6-trihydroxybenzophenoneC23H26O4366.46Aerial partZhang et al. (2017)
1232,4,6,3′,5′-PentamethoxylbenzophenoneC18H20O6332.35Aerial partQiu et al. (2015)
1242,4,6-TrihydroxybenzophenoneC13H10O4230.22Aerial partLin and Wu (2003)
1252,4,6-Trihydroxybenzophenone 3-C-geranyl etherC23H26O4366.46Aerial partLin and Wu (2003)
1262,4,6-Trihydroxybenzophenone 4-O-geranyl etherC23H26O4366.46Aerial partLin and Wu (2003)
1272,6-Dihydroxy-4,3′,5′-trihymethoxy-benzophenoneC16H16O6304.30Whole plantYin et al. (2013)
1282,6-Dihydroxy-4-[(E)-5-hydroxy-3,7-dimethylocta-2,7-dienyloxy]-benzophenoneC23H26O5382.46Whole plantDon et al. (2004)
1292,6-Dihydroxy-4-[(E)-7-hydroxy-3,7-dimethylocta-2-enyloxy]-benzophenoneC23H28O5384.46Whole plantDon et al. (2004)
1302-Hydroxy-4,6-dimethoxybenzophenoneC15H14O4258.27Aerial partQiu et al. (2015)
1312-β-D-glucopyranosyl-4,6-dihydroxyphenyl phenyl ketoneC19H20O9392.36Aerial partHong et al. (2004)
1323-(2-Hydroxy-7-methyl-3-methyleneoct-6-enyl)-5-isoprenyl-2,4,6-trihydroxybenzophenoneC28H34O5450.58Aerial partZhang et al. (2017)
1334-Geranyloxy-2,6-dihydroxybenzophenoneC23H26O4366.46Aerial partZhu et al. (2016a)
1344-Geranyloxy-2-hydroxy-6-isoprenyloxybenzophenoneC28H34O4434.58Aerial partHuang et al. (2020)
1358-Benzoyl-2,2-dimethyl-6-(E-3,7-dimethyl-2,6-octadi-enyl)-3,5,7-trihydroxy chromaneC28H34O5450.58Aerial partZhu et al. (2016a)
136Garcimangosone DC19H20O9392.36Whole plantChen et al. (2020)
137Otogirinin FC28H34O5450.58Aerial partTian (2015)
138Otogirinin GC28H34O5450.58Aerial partZhang et al. (2017)
139Petiolin FC19H20O10408.36Whole plantDung Nguyen et al. (2021)
140Sampbenzophenone AxC28H34O5450.58Aerial partZhu et al. (2016a)
141Sampbenzophenone BC28H34O5450.58Aerial partZhu et al. (2016a)
142Sampbenzophenone CC28H34O5450.58Aerial partZhu et al. (2016a)
143Sampbenzophenone DC23H26O5382.46Aerial partZhu et al. (2016a)
144Sampbenzophenone EC23H26O6398.46Aerial partZhu et al. (2016a)
145Sampbenzophenone FC22H26O6386.44Aerial partZhu et al. (2016a)
146Sampbenzophenone GC23H26O5382.46Aerial partZhu et al. (2016a)
147Sampsine AC16H16O6304.30Aerial partQiu et al. (2015)
148Sampsine BC22H26O10450.44Aerial partQiu et al. (2015)
149Sampsone FxC28H34O5450.58Aerial partTian (2015)
150Sampsone GC28H34O5450.58Aerial partTian (2015)

Benzophenones isolated from H. sampsonii.

x—Two compounds have the same structure while different names.

5.3 Xanthones

Xanthones, a class of iso-tricyclic compounds mainly divided into simple xanthones, glycosylated xanthones, prenylated xanthones, and sulfonated xanthones, are known to possess a variety of biological activities, such as antihypertensive, antiviral, and antitumor activities. In addition, the discrepancy in xanthones activity depends on the substituents on the aromatic rings.

In 1985, Chen MT and Chen CM isolated hyperxanthone (178) from the whole plant of H. sampsonii, and firstly discovered 2-hydroxy-3.4-dimethoxyxanthone (164) and isomangiferin (179) in the genus Hypericum (Chen and Chen, 1985). Further study on the constituents in the whole plant of H. sampsonii, Hong et al. also isolated two xanthone sulfonates, 1,3-dihydroxy-5-methoxyxanthone-4-sulfonate (158) and 1,3-dihydroxy-5-O-β-D-glucopyranosylxanthone-4-sulfonate (159) (Hong et al., 2004). The reported metabolites and structures of xanthones are shown in Supplementary Figure S5; Table 7.

TABLE 7

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
1511,3,5,6-Tetrahydroxy-2-prenylxanthoneC18H16O6328.32Whole plantDon et al. (2004)
1521,3,5,6-TetrahydroxyxanthoneC13H8O6260.20Whole plantDon et al. (2004)
1531,3,5-Trihydroxy-xanthoneC13H8O5244.20Aerial partGuo et al. (2007)
1541,3,6,7-Tetrahydroxy-8-(3-methyl-but-2-enyl)-xanthoneC18H16O6328.32Whole plantLi et al. (2004)
1551,3,6,7-Tetrahydroxy-xanthone (Norathyriol)C13H8O6260.20Whole plantDon et al. (2004)
1561,3-Dihydroxy-2-methoxyxanthoneC14H10O5258.23Whole plantShi et al. (2016)
1571,3-Dihydroxy-5-methoxyxanthoneC14H10O5258.23Whole plantDong et al. (2015)
1581,3-Dihydroxy-5-methoxyxanthone-4-sulfonateC14H9O8KS376.38Whole plantHong et al. (2004)
1591,3-Dihydroxy-5-O-β-D-glucopyranosylxanthone-4-sulfonateC19H17O13SK524.49Whole plantHong et al. (2004)
1601,6-DihydroxyxanthoneC13H8O4228.20Whole plantDon et al. (2004)
1611,7-Dihydroxy-2-methoxyxanthoneC14H10O5258.23Whole plantShi et al. (2016)
1621,7-Dihydroxy-4-methoxyxanthoneC14H10O5258.23Whole plantLi et al. (2004)
1631-Hydroxy-7-methoxy-9H-xanthen-9-oneC14H10O4242.23Whole plantChen et al. (2020)
1642-Hydroxy-3,4-dimethoxyxanthoneC15H12O5272.26Whole plantChen and Chen (1985)
1652-Hydroxy-5-methoxyxanthoneC14H10O4242.23Whole plantShi et al. (2016)
1662-HydroxyxanthoneC13H8O3212.20RootXiao et al. (2008)
1672-Methoxy-1,5-dihydroxyxanthoneC14H10O5258.23Aerial partXin et al. (2011a)
1682-MethoxyxanthoneC14H10O3226.23Aerial partZhang et al. (2017)
1695′-Demethoxycadensin GC23H18O9438.39Whole plantChen et al. (2020)
1705-Methoxy-1,3,7-trihydroxy xanthoneC14H10O6274.23Aerial partXin et al. (2011a)
1715-O-methyl-2-deprenyIrheediaxanthone BC19H18O6342.35Whole plantChen et al. (2020)
1727-Methoxy-1,5,6-trihydroxyxanthoneC15H12O6288.26Aerial partXin et al. (2011a)
173EuxanthoneC13H8O4228.20Aerial partHong et al. (2004)
174Hypericumxanthone AC19H18O6342.35Aerial partXin et al. (2011a)
175Hypericumxanthone BC23H22O6394.42Aerial partXin et al. (2011a)
176Hyperixanthone AC28H32O6464.56RootXiao et al. (2008)
1771,3,5,8-Tetrahydroxy-6-methoxy-7-isoprenylxanthoneC19H18O7358.35Whole plantDon et al. (2004)
178Hyperxanthone (5,9-Dihydroxy-3,3-dimethylpyrano [3,2-a]xanthen-12-one)C18H14O5310.31Whole plantChen and Chen (1985)
179IsomangiferinC19H18O11422.34Whole plantChen and Chen (1985)
180JacareubinC18H14O6326.30Whole plantChen et al. (2020)
181MangiferinC19H18O11422.34Whole plantChen and Chen (1985)
182NeolancerinC19H18O10406.34Whole plantDon et al. (2004)
183PadiaxanthoneC23H20O6392.41Whole plantDon et al. (2004)
184PatuloneC23H24O6396.44Whole plantLi et al. (2004)
185Sampsone CC18H18O8362.33Aerial partXin et al. (2011b)
186Toxyloxanthone BC18H14O6326.30Whole plantChen and Chen (1985)

Xanthones isolated from H. sampsonii.

5.4 Flavonoids

Flavonoids, including flavanols, biflavonoids, and common flavonoids, constitute an important class of metabolites in H. sampsonii. To date, twelve flavonoids have been isolated and identified from H. sampsonii (Supplementary Figure S6; Table 8). According to the documents, we have found that structures of these metabolites are generally based on the structure quercetin (193), in which the groups usually substitute at the 3- and 3′- positions, while all of saccharide groups located at C-3 in flavonoid glycosides.

TABLE 8

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
187(+)-CatechinC15H14O6290.27Whole plantChen et al. (2020)
1883,8″-BiapigeninC30H18O10538.46Whole plantDong et al. (2015)
189KaempferolC15H10O6286.24Whole plantDon et al. (2004)
190Kaempferol-3-O-glucopyranosideC21H20O11448.38Whole plantDon et al. (2004)
191LuteolinC15H10O6286.24Aerial partHong et al. (2004)
192NaringeninC15H12O5272.26Whole plantChen et al. (2020)
193QuercetinC15H10O7302.24Whole plantDon et al. (2004)
194Quercetin 3-galactoside (Hyperin, Hyperoside)C21H20O12464.38Whole plantZeng et al. (2002)
195Quercetin 3-O-glucopyranosideC21H20O12464.38Whole plantDon et al. (2004)
196Quercetin-3-O-arabinosideC20H18O11434.35Whole plantChen et al. (2020)
197QuercitrinC21H20O11448.38Whole plantChen et al. (2020)
198RutinC27H30O16610.52Whole plantChen et al. (2020)

Flavonoids isolated from H. sampsonii.

5.5 Naphthodianthrones

Naphthodianthrones, one out of the most biologically active substances in H. sampsonii, are mainly represented by hypericin and pseudohypericin (Supplementary Figure S7; Table 9). Hypericin (199), the active metabolite isolated from the flowers and fruits of H. sampsonii, is considered the characteristic constituent for the identification of this plant (Zeng et al., 2002). Subsequently, pseudohypericin (200) was isolated from the aerial parts of H. sampsonii (Zheng, 2005).

TABLE 9

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
199HypericinC30H16O8504.45Flower and fruitZeng et al. (2002)
200PseudohypericinC30H16O9520.45Aerial partZheng (2005)

Naphthodianthrones isolated from H. sampsonii.

5.6 Anthraquinones

Anthraquinones found in H. sampsonii generally include two types of single anthraquinones and bisanthraquinones. As shown in Supplementary Figure S8, compounds 201–204 are single anthraquinones, while compounds 205–207 are bisanthraquinones. The chemical structures of anthraquinones are listed in Table 10.

TABLE 10

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
2011,3,6-Trihydroxy-2-methylanthra-quinoneC15H10O5270.24Whole plantYin et al. (2013)
2023-Ethyl-1,8-dihydroxy-6-methoxyanthracene-9,10-dioneC17H14O5298.29Whole plantChen et al. (2020)
203EmodinC15H10O5270.24Whole plantDon et al. (2004)
204PhyscionC16H12O5284.27Whole plantQi et al. (2008)
205R-(−)-skyrin-6-O-β-D-glucopyranosideC36H28O15700.61Whole plantDon et al. (2004)
206R-(−)-skyrin-6-O-β-D-xylopyranosideC35H26O14670.58Whole plantDon et al. (2004)
207S-(+)-skyrin-6-O-β-D-glucopyranosideC36H28O15700.59Whole plantDon et al. (2004)

Anthraquinones isolated from H. sampsonii.

5.7 Simple aromatic compounds

Simple aromatic compounds in the extracts of H. sampsonii refer to the compounds with a benzene ring, which have simple structure and small relative molecular weight. The main compounds are presented in Supplementary Figure S9; Table 11. Xin WB and his co-works found a rare chemical structure sampsone B (218) in the aerial parts of H. sampsonii (Xin et al., 2011).

TABLE 11

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
2083,4-Dihydroxybenzoic acidC7H6O4154.12Whole plantKang et al. (2011)
2093,4-Dihydroxybenzoic acid ethyl esterC9H10O4182.18Whole plantYin et al. (2013)
2103,4-Dihydroxycinnamic acidC9H8O4180.16Aerial partHong et al. (2004)
2115,7-Dihydroxy-3-methylchromoneC10H8O4192.17Whole plantChen et al. (2020)
212Benzoic acidC7H6O2122.12Aerial partGuo et al. (2005)
213Caffeic acid methyl esterC10H10O4194.19Whole plantShi et al. (2016)
214Ferulic acidC10H10O4194.19Whole plantShi et al. (2016)
215Gallic acidC7H6O5170.12Whole plantChen et al. (2020)
216Octadecyl ferulateC28H46O4446.67Whole plantChen et al. (2020)
217P-hydroxybenzoic acidC7H6O3138.12Whole plantKang et al. (2011)
218Sampsone BC15H16O6292.29Aerial partXin et al. (2011b)
219Vanillic acidC8H8O4168.15Whole plantShi et al. (2016)

Simple aromatic compounds isolated from H. sampsonii.

5.8 Other secondary metabolites

In addition to the aforementioned compounds, other compounds including alkaloids, porphyrins, steroids, pentacyclic triterpenoids and so on have been found in H. sampsonii. Chen Q isolated 6-ethoxy-1H-pyrimidine-2,4-dione (220) from the whole plant of H. sampsonii (Chen et al., 2020). Qi JB and his colleagues found chlorophyll A (221) from the extract of H. sampsonii (Qi et al., 2008). Additionally, Chen Q also discovered β-sitosterol (222) from this plant (Chen et al., 2020). And Guo et al. isolated stigmasteol (223) from the aerial parts of H. sampsonii (Guo et al., 2005). Betulinic acid (224), a pentacyclic triterpenoid compound, was also discovered in this botanical drug (Don et al., 2004). Furthermore, this plant was also demonstrated to contain 2-caffeoyloxy-3-hydroxy-3-(3,4-dihydroxyphenyl) propyl alcohol (225) (Don et al., 2004), octacosanol (226) (Guo et al., 2005), and triacontanoic acid (227) (Guo et al., 2005). The variety and structure of other compounds are displayed in Supplementary Figure S10; Table 12.

TABLE 12

No.Compound nameMolecular formulaMolecular weightPart of the plantRef
2206-Ethoxy-1H-pyrimidine-2,4-dioneC6H8N2O3156.14Whole plantChen et al. (2020)
221Chlorophyll AC55H72MgN4O5893.51Whole plantQi et al. (2008)
222β-SitosterolC29H50O414.72Whole plantChen et al. (2020)
223StigmasterolC29H48O412.70Aerial partGuo et al. (2005)
224Betulinic acidC30H48O3456.71Whole plantDon et al. (2004)
2252-Caffeoyloxy-3-hydroxy-3-(3,4-dihydroxyphenyl) propyl alcoholC18H18O8362.33Whole plantDon et al. (2004)
226OctacosanolC28H58O410.76Aerial partGuo et al. (2005)
227Triacontanoic acidC30H60O2452.81Aerial partGuo et al. (2005)

Other compounds isolated from H. sampsonii.

6 Biological activities

Recent studies have revealed that several biological activities including anti-inflammatory, anti-tumor, anti-depressant, antiviral, antimicrobial, and antioxidant activities have been documented for extracts and secondary metabolites of H. sampsonii (Tian, 2015). These pharmacological effects have been summarized in Table 13; Figure 2.

TABLE 13

Biological activitiesExtracts/compoundsModelsPositive controlResultsRef
Anti-inflammatoryExtractsDimethyl benzene-induced acute ear edema and carrageenin-induced paw oedemaAspirinOedema↓Pei et al. (2004)
7-Epiclusianone (1)Carrageenin-induced paw edema in rats and LPS-induced peritonitis in miceIndomethacinPaw oedema↓, leukocyte recruitment↓Santa-Cecilia et al. (2011)
Hyperforatin F (13)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 15.26 μΜ, 13.05 μΜ, and 18.05 μΜ, respectivelyChen et al. (2020)
Hypericumone A (21)RAW 264.7 cellsAndrographolideIC50 = 40.32 μΜHuang et al. (2020)
Norhypersampsone A (73)RAW 264.7 cellsQuercetinIC50 = 30.2 μMZhang et al. (2017)
Otogirinin A (79)RAW 264.7 cellsAndrographolideIC50 = 32.87 μΜHuang et al. (2020)
Sampsonione J (99)RAW 264.7 cellsAndrographolideIC50 = 35.25 μΜHuang et al. (2020)
Sampsonol C (110)RAW 264.7 cellsIndomethacinIC50 = 27.3 μMXin et al. (2012)
Sampsonol F (113)RAW 264.7 cellsIndomethacinIC50 = 29.3 μMXin et al. (2012)
(E)-3-(3,7-dimethylocta-2,6-dienyl)2,4,6-trihydroxybenzophenone (121)RAW 264.7 cellsQuercetinIC50 = 37.1 μMZhang et al. (2017)
(Z)-3-(3,7-dimethylocta-2,6-dienyl)2,4,6-trihydroxybenzophenone (122)RAW 264.7 cellsQuercetinIC50 = 36.5 μMZhang et al. (2017)
4-geranyloxy-2,6-dihydroxybenzophenone (133)RAW 264.7 cellsQuercetinIC50 = 20.3 μMZhang et al. (2017)
Garcimangosone D (136)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 14.52 μΜ, 17.23 μΜ, and 19.14 μΜ, respectivelyChen et al. (2020)
Petiolin F (139)RAW 264.7 cellsCadamoninIC50 = 2.00 μMDung Nguyen et al. (2021)
Sampsine A (147)RAW 264.7 cellsCadamoninIC50 = 2.40 μMDung Nguyen et al. (2021)
Sampsine B (148)RAW 264.7 cellsCadamoninIC50 = 2.29 μMDung Nguyen et al. (2021)
1-hydroxy-7-methoxy-9H-xanthen-9-one (163)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 24.32 μΜ, 26.03 μΜ, 28.03 μΜ, respectivelyChen et al. (2020)
2-methoxyxanthone (168)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 34.15 μΜ, 31.76 μΜ, and 37.64 μΜ, respectivelyChen et al. (2020)
5′-Demethoxycadensin G (169)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 27.43 μΜ, 22.32 μΜ, and 37.64 μΜ, respectivelyChen et al. (2020)
5-O-methyl-2-deprenyIrheediaxanthone B (171)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 19.96 μΜ, 18.92 μΜ, and 22.03 μΜ, respectivelyChen et al. (2020)
Jacareubin (180)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 23.40 μΜ, 20.71 μΜ, and 26.65 μΜ, respectivelyChen et al. (2020)
Mangiferin (181)RAW 264.7, THP-1, AGS, NKE, MC3T3-E1, EA.hy926, ATDC5, 3T3-L1, primary mouse chondrocyte, human osteoarthritis chondrocyte, human renal glomerulus endothelial cell, and human oral epithelial cells; C57BL/6 mice, Balb/c mice, ICR mice, Swiss albino mice, Kunming mice, SD rats, and Wistar ratsInhibited the expression of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) and COX-2, iNOS, IL-8, IRF5; regulated NF-κB, PI3K/AKT, and MAPK/ERK pathwaysMei et al. (2021)
(+)-Catechin (187)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 25.31 μΜ, 26.29 μΜ, and 33.20 μΜ, respectivelyChen et al. (2020)
3,8″-Biapigenin (188)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 21.15 μΜ, 19.05 μΜ, and 25.34 μΜ, respectivelyChen et al. (2020)
Kaempferol (189)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 24.67 μΜ, 23.50 μΜ, and 29.57 μΜ, respectivelyChen et al. (2020)
Naringenin (192)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 29.60 μΜ, 25.51 μΜ, and 31.16 μΜ, respectivelyChen et al. (2020)
Quercetin (193)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 14.13 μΜ, 10.59 μΜ, and 15.92 μΜ, respectivelyChen et al. (2020)
Hyperoside (194)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 24.84 μΜ, 21.70 μΜ, and 26.87 μΜ, respectivelyChen et al. (2020)
Quercetin-3-O-arabinoside (197)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 40.32 μΜ, 31.82 μΜ, and 42.75 μΜ, respectivelyChen et al. (2020)
Quercitrin (197)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 36.92 μΜ, 30.66 μΜ, and 38.71 μΜ, respectivelyChen et al. (2020)
Rutin (198)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 32.35 μΜ, 27.17 μΜ, and 34.20 μΜ, respectivelyChen et al. (2020)
3-ethyl-1,8-dihydroxy-6-methoxyanthracene-9, 10-dione (202)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 16.21 μΜ, 14.11 μΜ, and 17.90 μΜ, respectivelyChen et al. (2020)
Emodin (203)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 17.06 μΜ, 12.39 μΜ, and 16.73 μΜ, respectivelyChen et al. (2020)
3,4-dihydroxybenzoic acid (208)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 29.03 μΜ, 25.91 μΜ, and 30.25 μΜ, respectivelyChen et al. (2020)
5,7-dihydroxy-3-methylchromone (211)BV-2 and RAW 264.7 cellsIndomethacinIC50 = 35.24 μΜ and 36.02 μΜChen et al. (2020)
Gallic acid (215)BV-2, RAW 264.7, and THP-1 cellsIndomethacinIC50 = 35.11 μΜ, 32.68 μΜ, and 38.42 μΜ, respectivelyChen et al. (2020)
6-ethoxy-1H-pyrimidine-2,4-dione (220)RAW 264.7 cellsIndomethacinIC50 = 41.69 μΜChen et al. (2020)
AntinociceptiveExtractsAcetic acid writhing test and hot-plate testMorphineWrithing responses↓, pain thresold↑Pei et al. (2004)
7-Epiclusianone (1)Acetic acid-induced writhing responses in mice, formalin test, hot plate test, and open-field testIndomethacin, morphineWrithing episodes↓, licking time↓, pain↓Santa-Cecilia et al. (2011)
Hyperforin (14)MiceInhibited the activity of PKCGaleotti et al. (2010)
AntitumorHyperforatin F (13)SMMC-7721 cellsCisplatinIC50 = 10.00 μΜGuo et al. (2017)
Hyperforin (14)CLL, CML, AML, U937 cells and breast cancer cellsInduced apoptosisSchiavone et al. (2014)
Hyperisampsin J (32)A549, HL-60, SMMC-7721, MCF-7, and SW480 cell linesIC50 = 0.53 μΜ, 0.56 μΜ, 0.58 μΜ, 0.88 μΜ, 2.49 μΜ, respectivelyBridi et al. (2018)
1,6-Dihydroxyxanthone (160)Hela cellsIC50 = 33.00 μΜWang et al. (2013)
Quercetin (193)U138MG, HeLa, U2-OS/MTX300, CWR22RV1, MDA-MB-453, HT-29, myeloid leukemia, and oral cavity cancer cell lines; CF1 mice, F344 rats, Wister rats, Min/+ mice, SD rats, CD-1 mice, and Swiss miceInhibited the proliferation of cancer cells; modulated the experimental carcinogenesisMurakami et al. (2008),Dajas (2012)
Rutin (198)MDA-MB-231, HTC, HT29, A549, MCF-7, SW480 cell lines; HPV16 transgenic mice, HR-1 hairless miceInduced the apoptosis in cancerous cells; COX2↓, inflammation↓Imani et al. (2021)
Hypericin (199)U87 MG, U937, and K562 cellsExhibited significant cytotoxic effectsXu et al. (2015),Misuth et al. (2017)
AntidepressantHyperforin (14)Forced swimming test in ratsImipramineReduced the immobility time, inhibited the reuptake of neurotransmittersNahrstedt and Butterweck (2010),Bridi et al. (2018)
Hyperoside (194)Forced swimming test in ratsImipramineReduced the immobility timeNahrstedt and Butterweck (2010)
Hypericin (199)Forced swimming test in ratsImipramineReduced the immobility timeNahrstedt and Butterweck (2010)
AntiviralHyperisampsin A (23)HIVEC50 = 2.97 μMBridi et al. (2018)
Hyperisampsin D (26)HIVEC50 = 0.97 μMBridi et al. (2018)
Hypersampsone A (38)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partLin and Wu (2003)
Hypersampsone B (39)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partLin and Wu (2003)
Hypersampsone C (40)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partLin and Wu (2003)
Hypersampsone D (41)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partLin and Wu (2003)
Hypersampsone E (42)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partLin and Wu (2003)
Hypersampsone F (43)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partLin and Wu (2003)
2,6-Dihydroxy-4-[(E)-5-hydroxy-3,7-dimethylocta-2,7-dienyloxy]-benzophenone (128)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partDon et al. (2004)
2,6-Dihydroxy-4-[(E)-7-hydroxy-3,7-dimethylocta-2-enyloxy]-benzophenone (129)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partDon et al. (2004)
Hyperxanthone (178)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partDon et al. (2004)
Kaempferol (189)H5N1Anti-H5N1Yin (2014)
Hypericin (199)HSV, HCV, HIV, MCMV, Sindbis virus, infectious bronchitis virus, and novel duck reovirusExhibited significant inhibitory activityBarnes et al. (2001),Zhang et al. (2022)
Pseudohypericin (200)HIV and HSVExhibited significant inhibitory activityBarnes et al. (2001)
R-(−)-skyrin-6-O-β-D-xylopyranoside (206)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partDon et al. (2004)
2-caffeoyloxy-3-hydroxy-3-(3,4-dihydroxyphenyl) propyl alcohol (225)HBV-producing cell line (MS-G2)Isolated from the anti-HBV partDon et al. (2004)
AntimicrobialRoot extractMDR S. aureusNorfloxacinMIC = 64 μg/mLXiao et al. (2007)
7-epiclusianone (1)MDR S. aureusNorfloxacinMIC = 4 μg/mLXiao et al. (2007)
Hyperforin (14)MRSA and PRSAMIC <6 μM; MIC = 0.1–1.0 μg/mLSchiavone et al. (2014),Bridi et al. (2018)
Peroxysampsone A (84)S. aureusNorfloxacinExhibited Comparable activity with the positive drugXiao et al. (2010)
Sampsone A (89)MRSAMIC = 32 μg/mLXin et al. (2011b)
4-geranyloxy-2,6-dihydroxybenzophenone (133)Klebsiella pneumoniae, Mycobacterium smegmatis, Pseudomonas aeruginosa, Salmonella gallinarum, and S. aureusExhibited inhibitory activityPecchio et al. (2006)
Hypericumxanthone A (174)MRSAMIC = 16 μg/mLXin et al. (2011b)
Hypericumxanthone B (175)MRSAMIC = 32 μg/mLXin et al. (2011a)
Quercetin (193)S. aureus, Pseudomonas aeruginosa, Streptococcus mutans, Streptococcus sobrinus, Lactobacillus acidophilu, Streptococcus sanguis, Actinobacillus actinomycetemocomitans, and Prevotella intermediaExhibited inhibitory activityNguyen and Bhattacharya (2022)
Hypericin (199)S. aureusStopped the growth of S. aureus when incubated with 40 μM combined with visible lightWölfle et al. (2014)
AntioxidantEthyl acetate extractBALB/c mice5-ASARegulated the levels of CAT, GSH, MDA, and SODLin et al. (2022)
Hyperforin (14)HaCaT cell lineTrolox and NacetylcysteineEC50 = 0.42 μg/mL, higher than Trolox (12 μg/mL) and Nacetylcysteine (847 μg/mL)Wölfle et al. (2014)
Mangiferin (181)DPPH assayIC50 = 35.48 μMDung Nguyen et al. (2021)
Kaempferol (189)DPPH assayShowed 66% scavenging activity at the concentration of 75 μMDeng et al. (2019)
Quercetin (193)DPPH assayInhibition of MAOStojanović et al. (2013)
Rutin (198)SH-SY5Y cell lineIncreased the production of SOD, CAT and GSHEnogieru et al. (2021)
Hypericin (199)MCF-7 cell lineIncreased the production of SOD-2 combined with photodynamic therapyKimáková et al. (2017)
Lipid-loweringHypersampone A (114)HepG2 cell lineRosiglitazoneInhibited the expression of FAS and ACACA at 5 μMHuang et al. (2022)

The biological activities of H. sampsonii.

FIGURE 2

6.1 Anti-inflammatory activity

In vitro studies have suggested that extracts of H. sampsonii showed anti-inflammatory activity in lipopolysaccharide (LPS)-treated BV-2, RAW 264.7, and THP-1 cells (Chen et al., 2020). On the other hand, in vivo studies have demonstrated that the alcohol extracts of H. sampsonii had antinociceptive and anti-inflammatory properties. The antinociceptive potential carried out using acetic acid-induced writhing responses in mice and hot-plate test suggested that extracts of H. sampsonii effectively suppressed the writhing symptom and increased the pain threshold of mice. Also, the anti-inflammatory effect was investigated using dimethyl benzene-induced acute ear edema and carrageenin-induced paw edema in rats. Besides, the anti-inflammatory activity have been demonstrated by the reduction of acute ear edema induced by dimethyl benzene and carrageenin-induced paw oedema (Pei et al., 2004). A study of our group to investigate the therapeutic effects and molecular mechanisms of H. sampsonii (HS) in a dextran sulfate sodium (DSS)-induced ulcerative colitis (UC) mice model (Lin et al., 2022). These results indicate that HS distinctly alleviated DSS-stimulated UC-like lesions symptoms as evidenced by a significant recovery from body weight, colon lengths, and histological injuries of colons. HS reduced the accumulation of pro-inflammatory cytokines and improved the mRNA level of IL-10. Simultaneously, the colonic mRNA expression levels of IL- 1β, IL-17, iNOS and COX-2 were all significantly suppressed by HS in a dose-dependent manner. Furthermore, HS restored the protein expression of tight junction-associated protein (ZO-1 and occluding). Further studies have also reported that HS can significantly inhibit the protein level of PDE4 and reduced the expressions of PKA and phosphorylated CREB.

Experimental evidence has emerged to indicate that PPAPs are one of the major constituents required for anti-inflammatory effects. Since, it has been reported that a series of compounds isolated from H. sampsonii, including hyperattenin C (3), otogirinin D (12), hyperisampsin I (15), hyperisampsin J (16), sampsonione L (28), hyperattenin G (38), hypersampsone O (63), hypersampsonone A (68), sampsonione A (85), and sampsonione B (86), were found to have significant PDE4D2 inhibitory activity (Zhang et al., 2016). PDE4D2 is one of the subtypes of phosphodiesterase-4 (PDE4), which can specifically hydrolyze cAMP and participate in various physiological responses, and is a promising drug target for inflammatory diseases such as psoriasis and ulcerative colitis. Moreover, the antinociceptive and anti-inflammatory properties have been reported for 7-epiclusianone (1) using animal models (Santa-Cecilia et al., 2011). In addition to PPAPs, other compounds such as benzophenone, xanthones, flavonoids, anthraquinones, and phenols, are also stated to possess anti-inflammatory properties (Chen et al., 2020).

Besides, benzophenone derivatives have also been shown to be important in the anti-inflammatory effects of H. sampsonii. Recently, our group investigated the therapeutic effect and potential mechanisms of 4-geranyloxy-2,6-dihydroxybenzophenonel (4-GDB, 133) on DSS-induced ulcerative colitis in mice (Wang et al., 2023). This study showed that intragastric administration of 4-GDB (20 mg/kg/day) for 8 days significantly attenuated colonic injury, reduced the expression of inflammatory mediators, and improved colonic barrier function in mice with colitis. Furthermore, in vivo and in vitro experiments indicated that 4-GDB could activate cAMP/PKA/CREB and inhibit the NF-κB pathway. Collectively, 4-GDB may be a potential agent for treating UC by regulating the cAMP/PKA/CREB and NF-κB pathways.

6.2 Antitumor activity

The antitumor activity of H. sampsonii has been evaluated in various cancer cell lines in vitro including A375, MDA-MB-231, SHSY-5Y, and SiHa cell lines (Chen et al., 2020). Studies have suggested that regulation of subcellular localization of retinoid X receptor-alpha (RXR-α) is a potential method to induce tumor cell apoptosis. Zeng et al. have found that H. sampsonii extracts can induce the translocation of RXR-α from the nucleus to the cytoplasm, and promote the apoptosis of NIH-H460, MGC-803, and SMMC-7721 (Jin-Zhang et al., 2006). Besides, the ethanol extract and the chloroform fraction especially were demonstrated for apoptosis-inducing and antitumor properties via inhibiting RXR-α transcription (Han et al., 2007).

Moreover, the antitumor effect has also been documented for a panel of natural products in H. sampsonii, such as 7-epiclusianone (1) (Sales et al., 2015), sampsonione A (85) (Hu and Sim, 1999a), sampsonione I (93) (Hu and Sim, 1999a), mangiferin (181) (Mei et al., 2021), naringenin (192) (Memariani et al., 2021), quercetin (193) (Murakami et al., 2008; Dajas, 2012) and rutin (198) (Imani et al., 2021).

6.3 Antidepressant activity

Depression is a common mental disorder characterized by syndromes like depressed mood, hopelessness, and even thoughts of suicide. Clinical studies have demonstrated that H. perforatum L. (St. John’s Wort), a member of the Hypericum genus, has significant antidepressant impacts. The extract of this plant was introduced into the market as an antidepressant in Germany in 1988, and became the preferred phytomedicine for the treatment of depressive disorder in European and American regions. Intriguingly, previously reported studies have also isloated an antidepressant active metabolite hyperforin rom H. perforatum and its also present in H. sampsonii (Zheng et al., 2003).

In 2003, the ethanol extracts of H. sampsonii were demonstrated for a significant antidepressant effect on the behavior despair animal models (Wan et al., 2003). It was believed that the total flavonoids of H. sampsonii showed antidepressant activity in the hypothermia experiments induced by reserpine and the forced swimming test. In studies utilizing the forced swimming test, tail suspension test, and open-field test, H. sampsonii extracts, HTX fraction, and mangiferin (181) induced a significant reduction in immobility, and the antidepressant mechanism of HTX might be related to neurotransmitters (Gong, 2014). The antidepressant properties of H. sampsonii have been attributed to various phytochemical constituents, such as hyperforin (6), hyperoside (194), and hypericin (199) (Nahrstedt and Butterweck, 2010; Bridi et al., 2018). However, the precise mechanism of action for the antidepressant capacity of this plant remains indistinct.

6.4 Antiviral activity

Previous studies have suggested that the extracts and several compounds of H. sampsonii have antiviral activity. For instance, the chloroform and n-butyl alcohol fractions as well as kaempferol (189) were shown to possess antiviral activity against avian influenza virus H5N1 in the Madin Darby Canine Kidney (MDCK) screening experiment (Yin, 2014). Besides, Lin and Wu found that hypersampsone A-F (52–56, 9) isolated from H. sampsonii exhibited anti-HBV activity on the MS-G2 cell line (Lin and Wu, 2003). In addition, the antiviral activity has been reported for hypericin (199) and pseudohypericin (200) against herpes simplex virus types 1 and 2 and HIV-1 in vitro. Hypericin (199) has also exhibited activity against HCV, murine cytomegalovirus (MCMV), Sindbis virus, infectious bronchitis virus, and novel duck reovirus (Barnes et al., 2001; Zhang et al., 2022).

6.5 Antimicrobial activity

Plants belonging to the Hypericum genus are a crucial source of antimicrobial compounds (Marrelli et al., 2016). Previous evidence indicated that the antibacterial activity has been demonstrated for hyperforin (6) and quercetin (193) against Staphylococcus aureus, Streptococcus mutans, Streptococcus pyogenes, and Corynebacterium diphtheria, etc (Barnes et al., 2001; Nguyen and Bhattacharya, 2022). In studies using MDR S. aureus strain SA-1199B to determine the antibacterial effect of H. sampsonii, the MIC of the petroleum ether extract of the root was up to 64 μg/mL (Xiao et al., 2007). Moreover, 7-epiclusianone (1) induced potent antibacterial activity against SA-1199B with a MIC of 4 μg/mL, while MIC of the positive control (norfloxacin) was 32 μg/mL (Xiao et al., 2007). In other antibacterial experiments, some PPAPs including sampsone A (107) and hypericumxanthone A (174) were shown to exhibit good antibacterial activity on Methicillin-resistant S. aureus (MRSA), with MIC values of 32 μg/mL and 16 μg/mL respectively (Xin et al., 2011).

6.6 Antioxidant activity

Reactive oxygen species (ROS), the important substances released from neutrophils, play a part in cell signaling and homeostasis. It is, however, important to note, that the overproduction of ROS can initiate the inflammatory cascade and subsequent cell damage as well as tissue dysfunction under oxidative stress (Chen et al., 2009). Research revealed that H. sampsonii showed antioxidant capacity by regulating the content of oxidase (GSH and SOD) (Chen et al., 2009). It has also been reported that the ethyl acetate extract of H. sampsonii could alleviate oxidative stress as indicated by reversing the abnormal levels of CAT, GSH, MDA, and SOD in mice with colitis (Lin et al., 2022). Additionally, the antioxidant activity of mangiferin (181) from H. sampsonii was assessed by means of the DPPH radical scavenging assay with an IC50 value of 35.48 μM (Dung Nguyen et al., 2021).

7 Safety

Many ancient classics and medicinal books have recorded that the clinical administration dosage of H. sampsonii should be 9–15 g for dried herb or 30–60 g for fresh herb. To further determine the safety of therapeutic doses of H. sampsonii, a previous study by Lin et al. (2022), fed mice with the ethyl acetate extract at a dose of 2000 mg/kg. After 14 days of observation, there was no morphological abnormality in major organs, indicating that the ethyl acetate extract of H. sampsonii showed no toxicity. Although the toxicity studies and the wide range of edible and medicinal values of H. sampsonii may provide a preliminary reference for its high safety in clinical application; however, the potential toxicity cannot be completely excluded.

According to the Chinese Materia Medica, morphological and microscopic examinations as well as physicochemical identification should be used to control the quality of H. sampsonii. Meanwhile, for its medicinal application, it is should also contain hypericin (199) and flavonoids (Editorial Board of Chinese Materia Medica, 1999). Yet, thin-layer chromatography (TLC) identification and content determination as well as other analytical methods have not been employed to control the quality of this plant, indicating a lack of quality standard despite its extensive folk utilization. Besides, there is no indication of potential safety issues. Therefore, further research work is essentially required to meet these standards.

8 Conclusion and perspectives

As a common botanical drug for the treatment of dysentery, enteritis, and irregular menstruation in folk, H. sampsonii is safe and effective. It is a versatile plant with a complexity of phytochemicals and remarkable pharmacological actions. In this paper, we reviewed the botany, traditional uses, phytochemistry, pharmacological activities, and safety of this species for the first time. It was found that more than 220 chemicals have been isolated and identified from this plant, including PPAPs, benzophenones, xanthones, flavonoids, naphthodianthrones, anthraquinones, and aromatic compounds, among others. Among the identified compounds, PPAPs are the most abundant compounds with novel structures as well as up-and-coming biological characteristics, such as PDE4 inhibitory activity. Although, accumulating studies have shown the progress in the understanding of its anti-inflammatory, anti-tumor, antidepressant, antiviral, antibacterial, and antioxidant properties. However, further studies should focused on the isolation of new compounds and biological screening tests in vitro from H. sampsonii. Yet, it is also important to mention that empirical pharmacologic studies are insufficient to validate the claimed healing properties.

It is noteworthy that H. perforatum L., the most familiar species of the Hypericum genus, has been extensively investigated due to its medicinal values and was listed in the Chinese Pharmacopoeia in 2015. Nevertheless, H. sampsonii has not yet been listed in the Chinese Pharmacopoeia, which potentially prevents in-depth research to a large extent. Taken together, the current pharmacological research on H. sampsonii remains in infancy, and other aspects such as safety evaluation and quality control standards are scanty. This review provided a systematic overview of this plant based on the available research while not comprehensive. Therefore, further studies including pharmacological mechanisms in vitro and in vivo, structure-activity relationship appraisal, safety evaluation, and quality standards should be done. More emerging studies may reveal the scientific connotation of the traditional application and lay the foundation for the development and utilization of H. sampsonii.

Statements

Author contributions

ZS: methodology, writing—original draft, writing—review and editing, funding acquisition, supervision. YL and RL: data curation. RZ: conceptualization, writing—original draft, funding acquisition. All authors contributed to the article and approved the submitted version.

Funding

This work was supported by the Science and Technology Program of Guangdong Province of China (2022B1212010014) and the Guangdong Province’s Projects of High-Level University Construction Funds (No. A1-2601-21-414-001Z06).

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.

Publisher’s note

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.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2023.1247675/full#supplementary-material

Abbreviations

CNKI, China National Knowledge Infrastructure; IC50, 50% Inhibitory concentration; uM, Micromolar; Pre, isoprenyl; Ger, geranyl; Bz, benzoyl.

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Summary

Keywords

Hypericum sampsonii Hance, botany, traditional uses, phytochemistry, biological activities, safety

Citation

Sun Z, Li Y, Zhong R and Li R (2023) Hypericum sampsonii Hance: a review of its botany, traditional uses, phytochemistry, biological activity, and safety. Front. Pharmacol. 14:1247675. doi: 10.3389/fphar.2023.1247675

Received

26 June 2023

Accepted

31 August 2023

Published

19 September 2023

Volume

14 - 2023

Edited by

Daqian Wan, Tongji Hospital Affiliated to Tongji University, China

Reviewed by

Changling Hu, North Carolina Agricultural and Technical State University, United States

Hong-Hua Wu, Tianjin University of Traditional Chinese Medicine, China

Updates

Copyright

*Correspondence: Zhanghua Sun, ; Ruimin Zhong,

†These authors contributed equally to this work

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.

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