二甲双胍对肠道微生物群的调节及其对非酒精性脂肪性肝病(NAFLD)的影响:网络药理学和分子动力学研究

IF 0.5 Q4 GENETICS & HEREDITY
Sarvesh Sabarathinam , Ramesh Venkatachalapathy , Akash Jayaraman
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引用次数: 0

摘要

非酒精性脂肪性肝病(NAFLD)涉及肝脏过度脂肪积累,肠道微生物群在其发展中起着至关重要的作用。二甲双胍是治疗2型糖尿病的常用药物,可影响肠道微生物群,影响NAFLD的管理。这项研究调查了二甲双胍如何改变肠道微生物以及这些变化如何影响身体功能。通过网络药理学、分子对接和动力学研究,我们确定了连接NAFLD和肠道代谢物的关键靶基因。分子动力学表明,AKT1和HSP0AA1配合物在溶剂环境中是稳定的。此外,GO和KEGG通路分析表明,这些靶基因参与脂质代谢途径。我们的研究结果增强了对二甲双胍通过肠道菌群调节对NAFLD影响的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Metformin's modulation of gut microbiota and its implications for Non-Alcoholic Fatty Liver Disease(NAFLD): A network pharmacology and molecular dynamics study

Metformin's modulation of gut microbiota and its implications for Non-Alcoholic Fatty Liver Disease(NAFLD): A network pharmacology and molecular dynamics study
Non-alcoholic fatty liver disease (NAFLD) involves excessive fat accumulation in the liver, with gut microbiota playing a crucial role in its development. Metformin, a common treatment for type 2 diabetes, affects gut microbiota, influencing NAFLD management. This study investigates how metformin modifies gut microbes and how these changes impact bodily functions. Using network pharmacology, molecular docking, and dynamics studies, we identified key target genes linking NAFLD and gut metabolites. Molecular dynamics revealed that AKT1 and HSP0AA1 complexes are stable in solvent environments. Additionally, GO and KEGG pathway analyses indicated that these target genes are involved in lipid metabolism pathways. Our findings enhance the understanding of metformin's impact on NAFLD through gut microbiota modulation.
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来源期刊
Human Gene
Human Gene Biochemistry, Genetics and Molecular Biology (General), Genetics
CiteScore
1.60
自引率
0.00%
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0
审稿时长
54 days
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