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含蒽醌、二苯乙烯苷类中药效-毒转换物质基础及作用机制研究进展
引用本文:商佳,郑彬茹,陶倩倩,刘睿,韦源青,韩疏影.含蒽醌、二苯乙烯苷类中药效-毒转换物质基础及作用机制研究进展[J].中草药,2023,54(19):6482-6496.
作者姓名:商佳  郑彬茹  陶倩倩  刘睿  韦源青  韩疏影
作者单位:南京中医药大学药学院, 江苏 南京 210023;南京中医药大学药学院, 江苏 南京 210023;南京中医药大学/江苏省中药资源产业化过程协同创新中心/中药资源产业化与方剂创新药物国家地方联合工程研究中心/国家中医药管理局中药资源循环利用重点研究室, 江苏 南京 210023;南京中医药大学, 江苏省海洋药用生物资源研究与开发重点实验室, 江苏 南京 210023;南京中医药大学药学院, 江苏 南京 210023;南京中医药大学, 江苏省海洋药用生物资源研究与开发重点实验室, 江苏 南京 210023
基金项目:国家自然科学基金资助项目(82174090);江苏省高校“青蓝工程”中青年学术带头人;江苏省高校333工程第三层次培养对象
摘    要:有毒中药效-毒转换机制的研究一直是中药合理应用的难点,以蒽醌类、二苯乙烯苷类成分及含有该类成分的中药为研究对象,梳理了这2类效-毒同源物质及其体内代谢规律与产物,分析了效-毒同源物质原型及其代谢产物的构-效与构-毒关系,整合并总结了含蒽醌、二苯乙烯苷类有毒中药的药效与毒性作用机制及毒-效转换关系与规律。为进一步阐释中药效-毒转换机制的研究,基于蛋白组学技术、药物靶点及药物作用机制研究方法,提出了以蒽醌类、二苯乙烯苷类成分为例的中药效-毒转换靶点与机制研究的策略与展望,为中药效-毒转换机制与转换规律的探究提供思路与方法借鉴。

关 键 词:效-毒转换  蒽醌  二苯乙烯苷  大黄素甲醚  大黄酚  芦荟大黄素  大黄酸  大黄素
收稿时间:2023/2/15 0:00:00

Research progress on substance basis and mechanism of traditional Chinese medicines containing anthraquinone and stilbene glycosides in effect-toxicity conversion
SHANG Ji,ZHENG Bin-ru,TAO Qian-qian,LIU Rui,WEI Yuan-qing,HAN Shu-ying.Research progress on substance basis and mechanism of traditional Chinese medicines containing anthraquinone and stilbene glycosides in effect-toxicity conversion[J].Chinese Traditional and Herbal Drugs,2023,54(19):6482-6496.
Authors:SHANG Ji  ZHENG Bin-ru  TAO Qian-qian  LIU Rui  WEI Yuan-qing  HAN Shu-ying
Institution:College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China;College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China;Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, National Administration of Traditional Chinese Medicine Key Laboratory of Chinese Medicinal Resources Recycling Utilization, Nanjing University of Chinese Medicine, Nanjing 210023, China;Jiangsu Key Laboratory of Research and Development in Marine Bio-Resource Pharmaceutics, Nanjing University of Chinese Medicine, Nanjing 210023, China;College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China;Jiangsu Key Laboratory of Research and Development in Marine Bio-Resource Pharmaceutics, Nanjing University of Chinese Medicine, Nanjing 210023, China
Abstract:The study of the efficacy-toxicity conversion mechanism of toxic traditional Chinese medicine (TCM) has always been a difficult point in the rational application of Chinese herbal medicine. In this paper, we have taken the anthraquinones, stilbene glycosides and TCM containing these components as the research objects, sorted out these two types of efficacy-toxicity homologous substances and their metabolism patterns and products in vivo, analyzed the efficacy-toxicity of prototypes of these homologous substances and structure-activity and structure-toxicity relationships of their metabolites, and integrated and summarized the mechanism of efficacy and toxicity, as well as the relationships and patterns of efficacy-toxicity conversion for toxic TCM containing anthraquinone and stilbene glycosides. To further elucidate the mechanism of the efficacy-toxicity conversion of TCM, we proposed strategies and prospects for the study of the targets and mechanism of efficacy-toxicity conversion of Chinese medicines based on proteomics technology, drug targets and drug mechanism of action by taking anthraquinones and stilbene glycosides as examples, in order to provide ideas and methodological reference for the investigation of the rules of efficacy-toxicity conversion of TCM.
Keywords:efficacy-toxicity conversion  anthraquinones  stilbenes glycosides  physcion  chrysophenol  aloe-emodin  rhein  emodin
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