Exploring the Mechanism of Si-miao-yong-an Decoction in the Treatment of Coronary Heart Disease based on Network Pharmacology and Experimental Verification

被引:2
|
作者
Zhang, Jingmei [1 ]
Xue, Siming [1 ]
Chen, Huan [1 ]
Jiang, Haixu [2 ]
Gao, Pengrong [3 ]
Lu, Linghui [3 ,4 ,5 ]
Wang, Qiyan [1 ,4 ,5 ]
机构
[1] Beijing Univ Chinese Med, Sch Life Sci, Beijing 100029, Peoples R China
[2] Beijing Univ Chinese Med, Sch Chinese Mat, Beijing 100029, Peoples R China
[3] Beijing Univ Chinese Med, Sch Tradit Chinese Med, Beijing 100029, Peoples R China
[4] Beijing Univ Chinese Med, Key Lab TCM Syndrome & Formula, Minist Educ, Beijing 100029, Peoples R China
[5] Beijing Key Lab TCM Syndrome & Formula, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Si-miao-yong-an decoction; network pharmacology; coronary heart disease; molecular docking; experimental verification; heart disease; TCMSP; ISCHEMIA-REPERFUSION INJURY; DIABETIC-RATS; ATHEROSCLEROSIS; APOPTOSIS; ANGIOGENESIS; TRANSITION; PREDICTION; KAEMPFEROL; MUSCLE; CELLS;
D O I
10.2174/1386207326666230703150803
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: To investigate the active ingredients and the mechanisms of Si-miao-yong-an Decoction (SMYA) in the treatment of coronary heart disease (CHD) by using network pharmacology, molecular docking technology, and in vitro validation.Methods: Through the Chinese Medicine System Pharmacology Database and Analysis Platform (TCMSP), Uniprot database, GeneCards database, and DAVID database, we explored the core compounds, core targets and signal pathways of the effective compounds of SMYA in the treatment of CHD. Molecular docking technology was applied to evaluate the interactions between active compounds and key targets. The hypoxia-reoxygenation H9C2 cell model was applied to carry out in vitro verification experiments. A total of 109 active ingredients and 242 potential targets were screened from SMYA. A total of 1491 CHD-related targets were retrieved through the GeneCards database and 155 overlapping CHD-related SMYA targets were obtained. PPI network topology analysis indicated that the core targets of SMYA in the treatment of CHD include interleukin-6 (IL-6), tumor suppressor gene (TP53), tumor necrosis factor (TNF), vascular endothelial growth factor A (VEGFA), phosphorylated protein kinase (AKT1) and mitogen-activated protein kinase (MAPK). KEGG enrichment analysis demonstrated that SMYA could regulate Pathways in cancer, phosphatidylinositol 3 kinase/protein kinase B (PI3K/Akt) signaling pathway, hypoxia-inducible factor-1(HIF-1) signaling pathway, VEGF signaling pathway, etc.Results: Molecular docking showed that quercetin had a significant binding activity with VEGFA and AKT1. In vitro studies verified that quercetin, the major effective component of SMYA, has a protective effect on the cell injury model of cardiomyocytes, partially by up-regulating expressions of phosphorylated AKT1 and VEGFA.Conclusion: SMYA has multiple components and treats CHD by acting on multiple targets. Quercetin is one of its key ingredients and may protect against CHD by regulating AKT/VEGFA pathway.
引用
收藏
页码:57 / 68
页数:12
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