首页|基于网络药理学探究清脉饮治疗下肢动脉硬化闭塞症的作用机制

基于网络药理学探究清脉饮治疗下肢动脉硬化闭塞症的作用机制

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目的 基于网络药理学技术,探究清脉饮治疗下肢动脉硬化闭塞症的潜在复杂机制.方法 通过多个数据库查找并筛选清脉饮活性成分及下肢动脉硬化相关基因,构建"药物-活性成分-靶点-疾病"网络,并进行基因本体论(GO)和京都基因与基因组百科全书(KEGG)富集分析及分子对接.结果 共筛选出清脉饮活性成分62种,主要涉及细胞信号传导(细胞增殖、细胞迁移、细胞凋亡等)、炎症反应、血管生成等方面;主要作用于肿瘤坏死因子(TNF)、丝氨酸/苏氨酸激酶1(AKT1)、甘油醛-3-磷酸脱氢酶(GAPDH)等靶点,参与磷脂酰肌醇3激酶(PI3K)-丝氨酸/苏氨酸激酶(AKT)、丝裂原活化蛋白激酶(MAPK)等信号通路.结论 此研究在网络药理学水平上,解释了清脉饮治疗下肢动脉硬化闭塞症的机制.
Discussion on the Mechanism of Qingmai Drink in Treating Lower Extremity Arteriosclerosis Occlusive Disease Based on Network Pharmacology
Objective To discuss the mechanism of Qingmai drink in treating lower extremity arteriosclerosis occlusive disease based on network pharmacology.Methods By searching and screening the active ingredients of Qingmai drink and the genes related to lower limb arteriosclerosis through multiple databases,the"drug-active ingredient-target-disease"network was constructed,and gene on-tology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analysis and molecular linkage were carried out.Re-sults A total of 62 active ingredients of Qingmai drink were screened,mainly related to cell signaling(cell proliferation,cell migration,cell apoptosis,etc.),inflammatory response,angiogenesis,etc.It mainly acts on tumor necrosis factor(TNF),serine/threonine kinase 1(AKT1),glyceraldehyde-3-phosphate dehydrogenase(GAPDH)and other targets,and participates in phosphatidylinositol 3 kinase(PI3K-serine/threonine kinase(AKT),mitogen-activated protein kinase(MAPK)and other signaling pathways.Conclusion The study explained the mechanism of Qingmai drink in treating ASO at the level of network pharmacology.

Qingmai drinklower extremity arteriosclerosis occlusive diseasenetwork pharmacology

乔丽蕊、凌银露、张磊

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上海中医药大学附属岳阳中西医结合医院血管外科,上海 200437

清脉饮 下肢动脉硬化闭塞症 网络药理学

2025

中国中医药现代远程教育
世中联(北京)远程教育科技发展中心

中国中医药现代远程教育

影响因子:0.531
ISSN:1672-2779
年,卷(期):2025.23(1)