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基于网络药理学的何首乌致肝损伤作用机制研究

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目的:通过网络药理学的技术和方法,筛选何首乌相关化学成分映射肝损伤作用靶点,构建何首乌成分-靶点-肝损伤网络图,探讨何首乌致肝损伤的作用机制.方法:通过TCMID、TCMGenDIT数据库及综合已报道文献检索何首乌化学成分,从中药系统药理学分析平台(TCMSP)、BATMAN-TCM数据库筛选并获取成分对应靶点;通过DrugBank、DisGeNET、GeneCards多数据库联合检索肝损伤靶点,整合分析交集靶点建立STRING蛋白交互关系,利用Cytoscape 3.7.1软件构建成分-靶点-肝损伤可视化网络;通过DAVID数据库对交集靶点基因功能(GO)分析和京都基因与基因组百科全书(KEGG)通路富集分析.结果:共筛选收集何首乌化学成分38个,成分靶点307个,肝损伤靶点6140个,成分与肝损伤交集靶点252个,GO生物功能富集分析共涉及838个,KEGG通路富集分析为111条,预测其涉及肝损伤作用机制通路主要包括cAMP信号通路、MAPK信号通路、非酒精性脂肪性肝病(NAFLD)、HIF-1信号通路、药物代谢-细胞色素P450、TNF信号通路、PI3K-Akt信号通路、NOD样受体信号通路、Toll样受体信号通路、Wnt信号通路.结论:进一步阐释了何首乌多成分、多靶点、多通路共同作用的特点,为解析何首乌致肝损伤作用机制研究提供新思路和新方向.
Study on the Mechanism of Liver Injury Induced by Polygonum Multiflorum Based on Network Pharmacology
Objective:To screen the target of liver damage by chemical constituents of Polygon um multiflorum by network pharmacology techniques and methods,and to construct a component-target-hepatic injury network map to explore the mechanism of liver damage caused by Polygonum multiflorum.Methods:The chemical constituents of Polygonum multiflorum were retrieved from the TCMID,TCMGenDIT database and the published literature,The TCMP and BATMAN-TCM databases were used to screen and obtain the corresponding targets.The results were searched by DrugBank,DisGeNET and GeneCards.Targets of liver injury,integrated analysis of intersection targets to establish STRING protein interactions,construction of component-target-hepatic injury visualization network using Cytoscape 3.7.1 software;analysis of target gene function(GO)by DAVID database and based on Kyoto Gene and Genomic Encyclopedia(KEGG)pathway enrichment analysis.Results:A total of 38 chemical components of Polygonum multiflorum,307 component targets,6140 liver injury targets,and 252 target of intersection of components and liver injury were collected,838 GO functional enrichment analysis,and KEGG pathway enrichment analysis was 111.It is predicted that the pathways involved in liver injury mainly include cAMP signaling pathway,MAPK signaling pathway,nonalcoholic fatty liver disease(NAFLD),HIF-1 signaling pathway,drug metabolism-cytochrome P450,TNF signaling pathway,PI3K-Akt Signaling pathway,NOD-like receptor signaling pathway,Toll-like receptor signaling pathway,Wnt signaling pathway.Conclusion:The characteristics of multi-component,multi-target and multi-channel interaction of Polygonum multiflorum were further explained,which provided new ideas and new directions for the study of the mechanism of liver injury induced by Polygonum multiflorum.

network pharmacologyliver injurytargetpathwaymechanism

梁幼玲、黄娟、白俊其、丘小惠

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广东创新科技职业学院医药健康学院,广东东莞 523960

广东省中医院,广东广州 510120

网络药理学 肝损伤 靶点 通路 机制

2024

广东化工
广东省石油化工研究院

广东化工

影响因子:0.288
ISSN:1007-1865
年,卷(期):2024.51(2)
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