基于网络药理学探讨便通灵胶囊治疗 脑卒中后便秘的作用机制
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徐前,男,主治中医师,主要研究方向是中西医结合治疗神经系统疾病。

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R 285

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贝敏敏江苏省名中医工作室建设项目[苏中医科教(2016)6 号];苏州市吴江区 “ 科教兴卫 ” 项目 (WWK202113)


Exploring the Mechanism of Bian Tong Ling Capsules in Treating Post-stroke Constipation Based on Network Pharmacology
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    摘要:

    摘 要目的:基于网络药理学探讨便通灵胶囊治疗脑卒中后便秘(PSC)的作用机制。 方法:通过检索中药系 统药理学数据库与分析平台(TCMSP)以及中药分子机制的生物信息学分析工具(BATMAN–TCM)筛选出便通灵 胶囊潜在活性成分及靶点,采用 GeneCards 数据库与在线人类孟德尔遗传数据系统(OMIM)获得 PSC 靶点,得到 药物与 PSC 的交集靶点,使用 Cytoscape 3.7.2 软件绘制活性成分靶点疾病交互网络图。采用 STRING 数据库构建靶 点蛋白质 – 蛋白质相互作用(PPI)网络,并应用 Metascape 数据库进行京都基因与基因组百科全书(KEGG)和基因 本体论(GO)富集分析。 结果:筛选后收集得到所有中药成分 189 个,收集疾病靶点 882 个,疾病与药物交集靶点共 31 个。PPI 网络提示核心靶点主要涉及到凋亡、趋化、炎症、细胞周期、增殖等方面。GO 富集主要包括蛋白酶 结合、整合素结合、对脂多糖的反应、细胞增殖的负调控、薄膜筏、细胞外基质等。KEGG 富集主要涉及脂质与动脉 粥样硬化信号通路、松弛素信号通路、癌症通路等。 结论:便通灵胶囊治疗 PSC 具有多成分、多靶点、多通路的作 用机制特点。

    Abstract:

    AbstractObjective To explore the mechanism of Bian Tong Ling Capsules in treating post-stroke constipation (PSC) based on network pharmacology. Methods Potential active components and targets of Bian Tong Ling Capsules were screened using the traditional Chinese medicine systems pharmacology database and analysis platform (TCMSP) and the bioinformatics analysis tool for molecular mechanisms of traditional Chinese medicine (BATMAN-TCM). PSC targets were obtained from the GeneCards datebase and online Mendelian inheritance in man (OMIM), and the intersecting targets between the drug and PSC were identified. Cytoscape 3.7.2 software was used to construct a network diagram of active component-target-disease interactions. The STRING database was utilized to build a protein-protein interaction (PPI) network of the targets, and Metascape datebase was applied for Kyoto encyclopedia of genes and genomes (KEGG) and gene ontology (GO) enrichment analyses. Results A total of 189 components of the herbal medicine and 882 disease targets were collected, with 31 intersecting targets between the drug and PSC identified. The PPI network indicated that the core targets mainly involved apoptosis, chemotaxis, inflammation, cell cycle, and proliferation. GO enrichment analysis mainly included protease binding, integrin binding, response to lipopolysaccharide, negative regulation of cell proliferation, membrane rafts, and extracellular matrix. KEGG enrichment analysis primarily involved lipid and atherosclerosis signaling pathways, relaxin signaling pathway, and cancer pathways. Conclusion The mechanism of Bian Tong Ling Capsules in treating PSC is characterized by multiple components, multiple targets, and multiple pathways.

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  • 收稿日期:2024-03-11
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  • 在线发布日期: 2024-08-22
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