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基于网络药理学和实验验证探讨四妙勇安汤治疗冠心病的作用机制。

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

机构信息

School of Life Sciences, Beijing University of Chinese Medicine, Beijing, 100029, China.

School of Chinese Materia, Beijing University of Chinese Medicine, Beijing, 100029, China.

出版信息

Comb Chem High Throughput Screen. 2024;27(1):57-68. doi: 10.2174/1386207326666230703150803.

Abstract

BACKGROUND

To investigate the active ingredients and the mechanisms of Si-miaoyong- 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 Gene- Cards 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, hypoxiainducible 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.

摘要

背景

采用网络药理学、分子对接技术和体外验证方法,研究四妙勇安汤(SMYA)治疗冠心病(CHD)的活性成分和作用机制。

方法

通过中药系统药理学数据库和分析平台(TCMSP)、Uniprot 数据库、GeneCards 数据库和 DAVID 数据库,探讨 SMYA 治疗 CHD 的有效化合物的核心化合物、核心靶点和信号通路。采用分子对接技术评价活性化合物与关键靶点的相互作用。应用缺氧/复氧 H9C2 细胞模型进行体外验证实验。从 SMYA 中筛选出 109 种活性成分和 242 个潜在靶点。通过 GeneCards 数据库检索到 1491 个与 CHD 相关的靶点,获得 155 个与 SMYA 治疗 CHD 相关的重叠靶点。PPI 网络拓扑分析表明,SMYA 治疗 CHD 的核心靶点包括白细胞介素-6(IL-6)、肿瘤抑制基因(TP53)、肿瘤坏死因子(TNF)、血管内皮生长因子 A(VEGFA)、磷酸化蛋白激酶(AKT1)和丝裂原激活蛋白激酶(MAPK)。KEGG 富集分析表明,SMYA 可调节癌症途径、磷脂酰肌醇 3 激酶/蛋白激酶 B(PI3K/Akt)信号通路、缺氧诱导因子-1(HIF-1)信号通路、VEGF 信号通路等。结果:分子对接表明,槲皮素与 VEGFA 和 AKT1 具有显著的结合活性。体外研究验证了 SMYA 的主要有效成分槲皮素对心肌细胞损伤模型具有保护作用,部分机制是通过上调磷酸化 AKT1 和 VEGFA 的表达。

结论

SMYA 具有多种成分,通过作用于多个靶点治疗 CHD。槲皮素是其关键成分之一,可能通过调节 AKT/VEGFA 通路来保护 CHD。

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