首页|探讨胃苓汤治疗代谢相关脂肪性肝病的网络药理学机制

探讨胃苓汤治疗代谢相关脂肪性肝病的网络药理学机制

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目的:探讨胃苓汤治疗代谢相关脂肪性肝病(MAFLD)的作用机制。方法:借助TCMSP及Uniprot数据库收集胃苓汤的活性成分并对其靶点进行基因名称校正,通过GeneCards、DisGeNET、OMIM数据库提取MAFLD的疾病靶点,分别将药物与疾病靶点导入Venny2。1 在线软件中获取共有靶点,利用Cytoscape 3。9。1 软件构建药物-活性成分-药物靶点互作网络。借助STRING数据库在线绘制蛋白相互作用网络,运用Metascape数据库对共有靶点进行GO功能及KEGG通路富集分析。结果:共收集胃苓汤活性成分158 个,其中槲皮素、柚皮素、山柰酚等是其治疗MAFLD的潜在核心成分。经筛选得到其治疗MAFLD的作用靶点有 121 个,涉及关键靶点PTGS2、ESR1、AR、PPARG等。结论:胃苓汤中多种成分具有治疗MAFLD活性,并通过多靶点及多途径发挥作用。
To Explore the Network Pharmacological Mechanism of Weiling Decoction in the Treatment of Metabolism-related Fatty Liver Disease
Objective:To investigate the mechanism of Weiling Decoction in the treatment of metabolism-related fatty liver disease(MAFLD).Methods:The active components of Weiling Decoction were collected by TCMSP and Uniprot database,and the gene names of the target were corrected,Disease targets of MAFLD were extracted from GeneCards,DisGeNET and OMIM databases,drug and disease targets were imported into Venny2.1 online software to obtain common targets,and drug-active components-drug target interaction network was constructed using Cytoscape 3.9.1 software.Using STRING database to map protein interaction networks online,The GO function and KEGG pathway enrichment of common targets were analyzed using Metascape database.Results:A total of 158 active ingredients of Weiling Decoction were collected,quercetin,naringenin and kaempferol are potential core components in the treatment of MAFLD.After screening,121 targets were identified for the treatment of MAFLD,it involves key targets PTGS2,ESR1,AR,PPARG,etc.Conclusion:Several components of Weiling Decoction have therapeutic activity for MAFLD,and play their roles through multi-target and multi-pathway.

metabolism-related fatty liver diseaseactive constituentdrug targetsweiling decoctionnetwork pharmacology

钟草源、程变巧

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福建中医药大学第二临床医学院,福建 福州 350122

福州市第二医院消化内科,福建 福州 350007

代谢相关脂肪性肝病 活性成分 药物靶点 胃苓汤 网络药理学

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(10)
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