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探讨桂枝茯苓丸治疗缺血性中风的疗效和药理机制:一项荟萃分析和网络药理学分析。

Exploring the therapeutic efficacy and pharmacological mechanism of Guizhi Fuling Pill on ischemic stroke: a meta-analysis and network pharmacology analysis.

机构信息

School of Rehabilitation Medicine, Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou, 450046, Henan, China.

School of Traditional Chinese Medicine, Henan University of Chinese Medicine, Zhengzhou, Henan, China.

出版信息

Metab Brain Dis. 2024 Aug;39(6):1157-1174. doi: 10.1007/s11011-024-01383-y. Epub 2024 Jul 25.

DOI:10.1007/s11011-024-01383-y
PMID:39052207
Abstract

The role of Guizhi Fuling Pill (GZFL) in the treatment of ischemic stroke (IS) is still controversial, and its pharmacological mechanism remains unclear. To evaluate the efficacy and potential pharmacological mechanisms of GZFL on IS, a comprehensive method integrating meta-analysis, network pharmacology, and molecular docking was employed. Eight electronic databases were searched from inception to November 2023. Review Manager 5.4.1 software was used for meta-analysis. Active compounds and targets of GZFL were retrieved from the Traditional Chinese Medicine Systems Pharmacology Database, Bioinformatics Analysis Tool for Molecular mechANism of Traditional Chinese Medicine, and Encyclopaedia of Traditional Chinese Medicine. Relevant targets of IS were obtained from the DisGeNet, Genecards, and DrugBank databases. GO biological function analysis and KEGG enrichment analysis were performed in the Metascape database. AutoDock Tools and PyMOL software were employed for Molecular docking. The intervention group significantly increased the total effective rate and decreased the NIHSS score. Administration of GZFL also improved the whole blood viscosity (low and high shear rates) and levels of fibrinogen, TNF-α, and IL-6. The key active compounds included quercetin, kaempferol, catechin, and beta-sitosterol, and the core target proteins included SRC, MAPK1, TP53, JUN, RELA, AKT1, and TNF. GO analysis mainly involved inflammation response, cellular response to lipids, and regulation of ion transport. The core pathways were lipid and atherosclerosis, cAMP, calcium, IL-17, and MAPK signaling pathways. Key active compounds showed good affinity with the core targets. The underlying mechanisms of GZFL in IS treatment are primarily related to its anti-inflammatory, anti-atherosclerosis, and neuroprotective effects.

摘要

桂枝茯苓丸治疗缺血性中风的作用仍存在争议,其药理机制尚不清楚。为了评估桂枝茯苓丸治疗缺血性中风的疗效和潜在药理机制,采用整合荟萃分析、网络药理学和分子对接的综合方法。从建库到 2023 年 11 月,检索了 8 个电子数据库。使用 Review Manager 5.4.1 软件进行荟萃分析。从中药系统药理学数据库与分析平台、中药分子机制生物信息分析工具和中药综合数据库中检索桂枝茯苓丸的活性化合物和靶点。从 DisGeNet、Genecards 和 DrugBank 数据库中获取缺血性中风的相关靶点。在 Metascape 数据库中进行 GO 生物功能分析和 KEGG 富集分析。使用 AutoDock Tools 和 PyMOL 软件进行分子对接。干预组总有效率显著提高,NIHSS 评分降低。桂枝茯苓丸还可改善全血黏度(高低切)和纤维蛋白原、TNF-α、IL-6 水平。关键活性化合物包括槲皮素、山奈酚、儿茶素和β-谷甾醇,核心靶蛋白包括 SRC、MAPK1、TP53、JUN、RELA、AKT1 和 TNF。GO 分析主要涉及炎症反应、细胞对脂质的反应和离子转运的调节。核心途径是脂质和动脉粥样硬化、cAMP、钙、IL-17 和 MAPK 信号通路。关键活性化合物与核心靶蛋白具有良好的亲和力。桂枝茯苓丸治疗缺血性中风的潜在机制主要与其抗炎、抗动脉粥样硬化和神经保护作用有关。

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