首页|基于网络药理学和分子对接探讨火土既济丹治疗勃起功能障碍的作用机制

基于网络药理学和分子对接探讨火土既济丹治疗勃起功能障碍的作用机制

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目的:基于网络药理学和分子对接探讨火土既济丹治疗勃起功能障碍(ED)的潜在作用机制.方法:利用TCMSP和TCMIP数据库筛选出火土既济丹中的主要有效化合物及其靶点;在Genecards数据库中获取ED的治疗靶点基因;利用Venny软件获得火土既济丹及ED的共同靶点,应用STRING数据库构建火土既济丹治疗ED的蛋白互作网络(PPI),再利用Cytoscape软件筛选出核心靶点,运用R软件对共有靶点进行GO功能分析和KEGG通路分析;最后利用Chem3D、AutoDock Tools及QuickVina-W软件对火土既济丹与核心靶点进行分子对接.结果:共获得有效化合物64个,药物靶点822个,疾病靶点1 783个,共同靶点320个.PPI网络分析得到火土既济丹治疗ED的核心靶点包括ESR1、HSP90AA1、SRC、STAT3等.GO功能分析结果显示共同靶点参与对异种刺激的反应、激酶活性的正向调节、MAPK级联反应的正向调控等生物过程.KEGG通路分析提示PI3K-Akt、凋亡、MAPK、HIF-1、VEGF、自噬等信号通路可能与火土既济丹治疗ED的机制有关.分子对接显示火土既济丹关键活性分子与核心靶点均有良好的对接活性.结论:本研究利用网络药理学和分子对接的方法揭示火土既济丹通过多成分、多靶点、多通路治疗ED,为临床治疗及后续的研究提供依据与参考.
Action mechanism of Huotu Jiji Pellets in the treatment of erectile dysfunction:An exploration based on network pharmacology and molecular docking
Objective:To explore the potential action mechanism of Huotu Jiji Pellets(HJP)in the treatment of erectile dys-function(ED)based on network pharmacology and molecular docking.Methods:We identified the main effective compounds and active molecular targets of HJP from the database of Traditional Chinese Medicine Systems Pharmacology(TCMSP)and Integrative Pharmacology-Based Research Platform of Traditional Chinese Medicine(TCMIP)and the therapeutic target genes of ED from the data-bases of Genecards.Then we obtained the common targets of HJP and ED using the Venny software,constructed a protein-protein in-teraction(PPI)network of HJP acting on ED,and screened out the core targets with the Cytoscape software.Lastly we performed GO functional enrichment and KEGG pathway enrichment analyses of the core targets followed by molecular docking of HJP and the core targets using Chem3D and AutoDock Tools and QuickVina-W software.Results:A total of 64 effective compounds,822 drug-related targets,1 783 disease-related targets and 320 common targets were obtained in this study.PPI network analysis showed that the core targets of HJP for ED included ESR1,HSP90AA1,SRC,and STAT3.GO functional enrichment analysis indicated the involvement of the core targets in such biological processes as response to xenobiotic stimulus,positive regulation of kinase activity,and positive regu-lation of MAPK cascade.KEGG pathway enrichment analysis suggested that PI3K-Akt,apoptosis,MAPK,HIF-1,VEGF,autophagy and other signaling pathways may be related to the mechanism of HJP acting on ED.Molecular docking prediction exhibited a good doc-king activity of the key active molecules of HJP with the core targets.Conclusion:This study showed that HJP acted on ED through multi-components,multi-targets and multi-pathways,which has provided some evidence and reference for the clinical treatment and subsequent studies of the disease.

Huotu Jiji Pelletserectile dysfunctionnetwork pharmacologymolecular docking

陈雪琴、周旋、沈宏平、宋佳怡、陈云杰、张元斌、蔡以力、余怡、刘亚华

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宁波大学附属第一医院传统医学中心,浙江宁波 315000

宁波大学附属第一医院药物临床试验机构,浙江宁波 315000

宁波大学附属第一医院生殖医学中心,浙江宁波 315000

宁波大学附属第一医院药学部,浙江宁波 315000

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火土既济丹 勃起功能障碍 网络药理学 分子对接

浙江省中医药科技计划项目宁波市重大科技任务攻关项目

2023ZR0492022Z148

2024

中华男科学杂志
南京军区南京总医院

中华男科学杂志

CSTPCD
影响因子:1.052
ISSN:1009-3591
年,卷(期):2024.30(3)