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A Network-Based Approach to Explore the Mechanism and Bioactive Compounds of Erzhi Pill against Metabolic Dysfunction-Associated Fatty Liver Disease

机译:一种基于网络的方法,探讨Erzhi丸对代谢功能障碍相关脂肪肝病的机制和生物活性化合物

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Erzhi pill (EZP), a classical traditional Chinese medicine prescription, exerts a potent hepatoprotective effect against metabolic dysfunction-associated fatty liver disease (MAFLD), previously known as nonalcoholic fatty liver disease (NAFLD). However, the mechanism and bioactive compounds underlying the hepatoprotective effect of EZP have not been fully elucidated. In this study, a systematic analytical platform was built to explore the mechanism and bioactive compounds of EZP against MAFLD. This was carried out through target prediction, protein-protein interaction (PPI) network construction, gene ontology, KEGG pathway enrichment, and molecular docking. According to the topological parameters of the PPI network, compound-target-pathway network, 9 targets, and 11 bioactive compounds were identified as core targets and bioactive compounds for molecular docking. The results showed that EZP exerts anti-MAFLD effects through a multicomponent, multitarget, multipathway manner, and luteolin and linarin may be the bioactive compounds of EZP. This study provides further research insights and helps explore the hepatoprotective mechanism of EZP.
机译:古典中医处方埃尔岛药丸(EZP)对代谢功能障碍相关的脂肪肝病(MAFLD)施加有效的肝脏保护作用,以前称为非酒精性脂肪肝病(NAFLD)。然而,尚未完全阐明了EZP的肝保护作用的机制和生物活性化合物。在这项研究中,建立了一个系统的分析平台,以探讨EZP对MAFLD的机制和生物活性化合物。这是通过靶预测,蛋白质 - 蛋白质相互作用(PPI)网络构建,基因本体,Kegg途径富集和分子对接进行。根据PPI网络的拓扑参数,将复合靶途径网络,9个靶标和11种生物活性化合物鉴定为用于分子对接的核心靶标和生物活性化合物。结果表明,EZP通过多组分,多元靶,多路径方式和木犀草素和Linarin施加抗MAFLD效应,也可以是EZP的生物活性化合物。本研究提供了进一步的研究见解,有助于探索EZP的肝脏保护机制。

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