基于网络药理学的丹参治疗视网膜静脉阻塞作用机制研究
投稿时间:2020-04-22     点此下载全文
引用本文:刘自强,农璐琪,韩梦雨,訾迎新,孟欢,邓宇,邓婷婷,金明.基于网络药理学的丹参治疗视网膜静脉阻塞作用机制研究[J].中国现代中药,2021,23(5):800-806
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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
刘自强 LIU Zi-qiang 北京中医药大学,北京102488 Beijing University of Chinese Medicine,Beijing 102488,China  
农璐琪 NONG Lu-qi 北京中医药大学,北京102488 Beijing University of Chinese Medicine,Beijing 102488,China  
韩梦雨 HAN Meng-yu 北京中医药大学,北京102488 Beijing University of Chinese Medicine,Beijing 102488,China  
訾迎新 ZI Ying-xin 北京中医药大学,北京102488 Beijing University of Chinese Medicine,Beijing 102488,China  
孟欢 MENG Huan 北京中医药大学,北京102488 Beijing University of Chinese Medicine,Beijing 102488,China  
邓宇 DENG Yu 北京中医药大学,北京102488 Beijing University of Chinese Medicine,Beijing 102488,China  
邓婷婷 DENG Ting-ting 中日友好医院 眼科,北京100029 Department of Ophthalmology,China-Japan Friendship Hospital,Beijing 100029,China  
金明 JIN Ming 中日友好医院 眼科,北京100029 Department of Ophthalmology,China-Japan Friendship Hospital,Beijing 100029,China 金明,教授,博士生导师,研究方向:中医药防治眼底病;E-mail:jinmingyk@163.com 
基金项目:国家自然科学基金项目(81574029);中医药传承与创新“百千万”人才工程(岐黄工程)岐黄学者项目
中文摘要:目的:探讨丹参治疗视网膜静脉阻塞(RVO)的作用机制。方法:采用中药系统药理学数据库与分析平台(TCMSP)检索丹参的有效化学成分,并收集其对应的作用靶点;使用GeneCards数据库检索与RVO相关的靶点;采用ClusterProfiler R软件绘制交集靶点的韦恩图;采用STRING 11.0数据库构建蛋白质-蛋白质相互作用(PPI)网络,采用Cytoscape 3.7.2 软件构建“药物-活性成分-疾病-靶蛋白”相互作用网络;采用ClusterProfiler R 软件对靶点进行基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析。结果:得到丹参有效成分41个、药物靶点70个、RVO靶点1705个,最终获得丹参治疗RVO的潜在作用靶点46个,KEGG通路76条。结论:丹参可能通过调控炎症反应、血管生成、凝血过程和细胞凋亡等对RVO发挥治疗作用。
中文关键词:丹参  视网膜静脉阻塞  网络药理学  作用机制
 
Exploration Mechanism of Salvia miltiorrhiza in Treating Retinal Vein Occlusion Based on Network Pharmacology
Abstract:Objective:To explore the pharmacological mechanism of Salvia miltiorrhiza in the treatment of retinal vein occlusion(RVO). Methods:The active components of S.miltiorrhiza were screened through Traditional Chinese Medicine Database and Analysis Platform(TCMSP),and the corresponding targets were collected;related targets of RVO were screened through GeneCards database;ClusterProfiler R software was used to draw the Venn diagram of intersection targets;STRING 11.0 database was used for protein-protein interaction(PPI) network;Cytoscape 3.7.2 was used to construct the network of “drug-component-disease-target”. Finally,the gene ontology(GO) and Kyoto encyclopedia of genes and genomes(KEGG) enrichment analysis of key targets were carried out by using the ClusterProfiler R software. Results:There were 41 active components and 79 targets for S.miltiorrhiza. There were 1705 disease-related targets. Finally,there were 46 potential targets for action and 70 KEGG pathways obtained. Conclusion:S.miltiorrhiza might play a role in the treatment of RVO through regulating inflammation response,angiogenesis,coagulation process,apoptosis and so on.
keywords:Salvia miltiorrhiza Bge.  retinal vein occlusion  network pharmacology  mechanism
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