基于组分配伍探讨黄连 黄芩保肝的物质基础
投稿时间:2018-06-05     点此下载全文
引用本文:段玉红,苏虹霞,杨红莲.基于组分配伍探讨黄连 黄芩保肝的物质基础[J].中国现代中药,2018,20(12):1483-1488
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作者中文名作者英文名单位中文名单位英文名E-Mail
段玉红 DUAN Yu-hong 陕西中医药大学 附属医院 内分泌二科,陕西咸阳712000 Department of Endocrinology,Affiliated Hospital of Shaanxi University of Chinese Medicine,Xianyang 712000,China  
苏虹霞 SU Hong-xia 陕西中医药大学 附属医院 内分泌二科,陕西咸阳712001 Department of Endocrinology,Affiliated Hospital of Shaanxi University of Chinese Medicine,Xianyang 712001,China  
杨红莲 YANG Hong-lian 陕西中医药大学 附属医院 内分泌二科,陕西咸阳712002 Department of Endocrinology,Affiliated Hospital of Shaanxi University of Chinese Medicine,Xianyang 712002,China 杨红莲,博士,副主任医师,研究方向:中药药性基础和临床研究;E-mail:465134440@qq.com 
基金项目:国家自然科学基金(81774304)
中文摘要:目的:采用分子E对接技术研究黄连、黄芩保肝的物质基础。方法:依据口服利用度、类似药、化合物的分子量等筛选黄连、黄芩的化学成分,采用iGEMDOCK软件对黄连、黄芩中28个化学成分与CYP1A2、CYP2E1、CYP2D6、CYP2C9、CYP3A4进行能量匹配,通过Cytoscape软件构建黄连、黄芩有效成分-CYP450网络模型。结果:28个化合物与CYP1A2、CYP2E1、CYP2D6、CYP2C9结合稳定,与CYP3A4结合较不稳定。黄连、黄芩共有10个化学成分同时与CYP1A2结合,3个成分与CYP2C9结合,抑制其活性。而黄芩还可以抑制CYP2E1、CYP2D6的活性。配伍比单味用药可能保肝效果更好。结论:发现CYP450酶系可能是黄连、黄芩保肝的作用靶点,尤其是CYP1A2和CYP2C9,抑制其活性,减少毒物N-乙酸-对苯醌亚胺生成,降低肝细胞损伤,达到保肝作用,为进一步研究黄连、黄芩保肝的分子机制提供理论依据。
中文关键词:黄连  黄芩  化学成分  保肝  分子对接  CYP450
 
Investigation of Material Basis for Protecting Liver in Coptis chinensis and Scutellaria baicalensis Based on Component Compatibility
Abstract:Objective:To study the material basis for protecting liver in Coptis chinensis and Scutellaria baicalensis based on molecular docking.Methods:The chemical constituents of Coptidis Rhizoma and Radix Scutellariae were screened based on oral availability,similar drugs and molecular weight of compounds,energy matching of 28 chemical constituents from Coptidis Rhizoma and Radix Scutellariae with CYP2D6,CYP2C9 and CYP3A4 were carried out by using iGEMDOCK Software,the network model of effective components of Coptidis Rhizoma and Radix Scutellariae was constructed by Cytoscape.Results:The combination of 28 compounds was stable with CYP1A2,CYP2E1,CYP2D6,CYP2C9,and instable with CYP3A4,there were 11 chemical constituents of Coptidis Rhizoma and Radix Scutellariae combined with CYP1A2 at the same time,three constituents of them bound to CYP2C9 to inhibit their activity.Radix Scutellariae also inhibited the activities of CYP2E1 and CYP2D6.Conclusion:It was found that the enzyme system of CYP450 might be the target of protecting liver of Coptidis Rhizoma and Radix Scutellariae,especially CYP1A2 and CYP2C9,which inhibited its activity and reduced the production of N-acetic acid-p-benzoquinone imine,reduced the damage of hepatocytes to protect the liver.It provides theoretical basis for further study of the molecular mechanism of Coptidis Rhizoma and Radix Scutellariae.
keywords:Coptis chinensis  Scutellaria baicalensis  chemical constituents  liver protection  molecular docking  CYP450
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