升阳散火汤治疗糖尿病周围神经病变的作用机制及网络药理学研究

Ying Wang, Lei Hua, Guoqiang Chen, Zhen-Han Li, Zhong-Pei Chen
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引用次数: 0

摘要

目的:应用网络药理学方法探讨升阳散活汤治疗糖尿病周围神经病变的作用机制。方法:采用BATMAN-TCM数据库、TCM-ID数据库、中国天然产物化学成分数据库和tcm - ip数据库,根据《利宾斯基药物规则》对生养散活汤中各草药的化学有效成分进行筛选。使用SwissTargetPrediction筛选处方中各草药的有效作用靶点。此外,利用Cytoscape 3.7.0构建“药物靶点”网络。利用GeneCards、OMIM和MaLaCards数据库收集与糖尿病周围神经病变相关的靶点。利用VENNY 2.1在线平台对药物和疾病靶点进行匹配,绘制维恩图,利用Cytoscape 3.7.0构建“药物活性化合物-常见靶点”网络。使用DAVID 6.8数据库对靶点进行基因本体生物学过程分析和京都基因与基因组百科全书通路富集分析。利用OmicShareTool在线平台将富集分析结果可视化。使用CB-Dock2进行分子对接。结果:经筛选,生养散活汤共鉴定出217种有效化合物和132种潜在靶点。这种作用主要集中在脂质和动脉粥样硬化、糖尿病并发症中的AGE-RAGE信号通路和IL-17信号通路等途径。关键活性成分与DPN核心蛋白靶点的结合能较好。结论:本研究揭示了升阳三活汤多靶点、多通路的特点,为该方的临床应用提供了新的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The active mechanism of the Sheng Yang San Huo decoction on diabetic peripheral neuropathy on network pharmacology
Objectives: To discuss the mechanism of Sheng Yang San Huo decoction on diabetic peripheral neuropathy using the network pharmacology method. Methods: The BATMAN-TCM database, TCM-ID database, Chinese Natural Product Chemical Composition Database, and TCMIP database were employed to screen the chemical active ingredients of each herb in Sheng Yang San Huo decoction based on the “Libinsky Drug Rules”. SwissTargetPrediction was used to screen effective action targets for each herb in the prescription. Additionally, Cytoscape 3.7.0 was utilized to construct a “drug-target” network. GeneCards, OMIM, and MaLaCards databases were utilized to gather targets related to diabetic peripheral neuropathy. VENNY 2.1 online platform was employed to match drug and disease targets, draw a Venn diagram, and construct a “drug-active compounds-common target” network using Cytoscape 3.7.0. gene ontology biological process analysis and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis for the targets were conducted using the DAVID 6.8 database. Enrichment analysis results were visualized using the OmicShareTool online platform. Molecular docking was performed using CB-Dock2. Results: Following screening, a total of 217 active compounds and 132 potential targets were identified in Sheng Yang San Huo decoction. The effects are primarily enriched in pathways such as Lipid and Atherosclerosis, AGE-RAGE signaling pathway in diabetic complications, and the IL-17 signaling pathway. The binding energy of the key active ingredients to the core protein targets of DPN was favorable. Conclusion: The study reveals the characteristics of multiple targets and pathways of Sheng Yang San Huo decoction, providing new insights for the clinical application of this prescription.
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