Hepatic Effect of 2,3,5,4'-tetrahydroxystilbene-2-O-β-D-glucoside, the Signature Component of Traditional Chinese Medicine Heshouwu: Advances and Prospects.

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Cheng-Yu Wang, Ying-Huan Hu, Zhen-Xiao Sun
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引用次数: 0

Abstract

Traditional Chinese medicine Heshouwu, named Polygoni Multiflori Radix in Pharmacopoeia of the People's Republic of China (PPRC, 2020), is derived from the root tuber of Polygonum multiflorum Thunb., Heshouwu or processed Heshouwu is well known for its function in reducing lipids and nourishing the liver. However, increasing cases of Heshouwu-induced hepatotoxicity were reported in recent years. Researchers have begun to study the paradoxical effects of Heshouwu on the liver. 2,3,5,4'-tetrahydroxystilbene-2-O-β-D-glucoside (TSG), an abundant functional component of Heshouwu, shows various biological activities, among which its effect on the liver is worthy of attention. This paper reviews the current studies of TSG on hepatoprotection and hepatotoxicity, and summarizes the doses, experimental models, effects, and mechanisms of action involved in TSG's hepatoprotection and hepatotoxicity, aiming to provide insight for future study of TSG and understanding the effects of Heshouwu on the liver. Emerging evidence suggests that TSG ameliorates both pathological liver injury and chemical-induced liver injury by modulating lipid metabolism, inhibiting the inflammatory response and oxidative stress in the liver. However, with the reports of clinical cases of Heshouwu induced liver injury, it has been found that long-term exposure to a high dose of TSG cause hepatocyte or hepatic tissue damage. Moreover, TSG may cause hepatotoxicity by affecting the transport and metabolism of other possible hepatoxic compounds in Heshouwu. Studies indicate that trans-TSG can be isomerized into cis-TSG under illumination, and cis-TSG had a less detrimental dose to liver function than trans- TSG in LPS-treated rats. In brief, TSG has protective effects on the liver, but liver injury usually occurs under highdose TSG or is idiosyncratic TSG-induced liver injury.

中药贺寿五标志性成分2,3,5,4′-四羟基二苯乙烯-2- o -β- d -葡萄糖苷的肝作用研究进展与展望
中药何首乌,在《中华人民共和国药典》(PPRC, 2020)中被命名为何首乌,是由何首乌的块根提取而成。和首乌以降脂养肝而闻名。然而,近年来,合首武引起的肝毒性病例越来越多。研究人员已经开始研究何首乌对肝脏的矛盾作用。2,3,5,4'-四羟基二苯乙烯-2- o -β- d -葡萄糖苷(TSG)是合首乌丰富的功能成分,具有多种生物活性,其中对肝脏的作用值得关注。本文综述了TSG在肝保护和肝毒性方面的研究现状,并对TSG在肝保护和肝毒性方面的剂量、实验模型、作用及其作用机制进行了总结,旨在为今后TSG的研究提供思路,了解和首武对肝脏的作用。新出现的证据表明,TSG通过调节肝脏脂质代谢、抑制炎症反应和氧化应激,改善病理性肝损伤和化学诱导的肝损伤。然而,随着合首乌致肝损伤临床病例的报道,发现长期暴露于高剂量的TSG可引起肝细胞或肝组织损伤。此外,TSG可能通过影响合首乌中其他可能的肝氧化化合物的转运和代谢而引起肝毒性。研究表明,在光照下,反式TSG可以异构化为顺式TSG,并且在lps处理的大鼠中,顺式TSG对肝功能的危害剂量小于反式TSG。总之,TSG对肝脏有保护作用,但肝损伤通常发生在高剂量TSG下,或者是TSG特异性诱导的肝损伤。
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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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