基于网络药理学分析国医大师沈宝藩痰瘀同治方防治高脂血症和动脉粥样硬化的作用机制
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R289

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广东省科技创新战略专项资金(科技基础条件建设领域)(2018B030322012)


Network Pharmacology-Based Analysis of Mechanism of National Traditional Chinese Medicine Master SHEN Baofan's Tanyu Tongzhi Prescription in Prevention and Treat⁃ ment of Hyperlipidemia and Atherosclerosis
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    目的:基于网络药理学和分子对接技术分析国医大师沈宝藩痰瘀同治方防治高脂血症和动脉粥样 硬化的作用机制。方法:通过中药系统药理分析数据库(TCMSP) 筛选痰瘀同治方的活性化合物,结合TTD、 DrugBank、GeneCards等数据库获取痰瘀同治方治疗高脂血症和动脉粥样硬化的作用靶点。采用Cytoscape3.8.2 绘制药物-成分-共有靶点网络图,再使用STRING 系统进行蛋白质-蛋白质相互作用网络分析,并使用 Metascape工具对痰瘀同治方治疗高脂血症和动脉粥样硬化的共有靶点进行GO功能富集分析和KEGG通路富集 分析,最后通过Autodock软件进行分子对接验证。结果:最终获得痰瘀同治方有效活性成分89个,潜在作用 靶点210个,与疾病靶点交集后得到124个交集基因。筛选得到槲皮素、丹参酮ⅡA、木犀草素、豆甾醇等主 要活性成分,TNF、IL-6、MMP9、CASP3、PTGS2等关节靶点。GO功能富集分析发现生物过程主要与类固醇 激素反应、氧化应激反应等相关。KEGG 分析发现脂质与动脉粥样硬化、流体剪切应力与动脉粥样硬化、 AGE-RAGE、IL-17、TNF等重要信号通路。分子对接结果显示主要活性成分与核心靶点结合活性较好。结论: 痰瘀同治方中槲皮素、丹参酮ⅡA、木犀草素、豆甾醇等有效活性成分可能通过对TNF、IL-6、MMP9、 CASP3、PTGS2等核心靶点进行调节,进而减轻炎症反应,最终治疗高脂血症和动脉粥样硬化。

    Abstract:

    Abstract:Objective:To analyze the mechanism of national traditional Chinese medicine master SHEN Baofan's Tanyu Tongzhi Prescription in the prevention and treatment of hyperlipidemia and atherosclerosis based on network pharmacology and molecular docking technology. Methods: Active compounds of Tanyu Tongzhi Prescription were screened from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP). Targets for treating hyperlipidemia and atherosclerosis were obtained by integrating databases such as TTD,DrugBank, and GeneCards. Cytoscape 3.8.2 was used to construct a drug-component-common target network. Protein-protein interaction network analysis was performed using the STRING system. GO functional enrichment analysis and KEGG pathway enrichment analysis of common targets were conducted via Metascape. Finally,molecular docking verification was performed with AutoDock software. Results:A total of 89 effective active components and 210 potential targets of Tanyu Tongzhi Prescription were obtained. After intersecting with disease targets, 124 overlapping genes were identified. Major active components included quercetin, tanshinone Ⅱ A, luteolin, and stigmasterol. Key targets included TNF, IL-6, MMP9, CASP3, and PTGS2. GO enrichment analysis showed that biological processes were mainly related to steroid hormone response and oxidative stress response. KEGG analysis highlighted important signaling pathways such as lipid and atherosclerosis, fluid shear stress and atherosclerosis, AGE-RAGE, IL-17, and TNF. Molecular docking results indicated good binding activity between the main active components and core targets. Conclusion: Effective active components in Tanyu Tongzhi Prescription, such as quercetin, tanshinone Ⅱ A, luteolin,and stigmasterol,may regulate core targets including TNF,IL-6,MMP9,CASP3,and PTGS2,thereby reducing inflammatory responses and ultimately treating hyperlipidemia and atherosclerosis.

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范琦铃,欧紫荆,潘锐焕.基于网络药理学分析国医大师沈宝藩痰瘀同治方防治高脂血症和动脉粥样硬化的作用机制[J].新中医,2026,58(10):206-217

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  • 在线发布日期: 2026-05-28
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