To Explore Mechanism of Xinmaikang Tablets in Treatment of Atherosclerosis Cardiovascular Disease Based on Network Pharmacology and Cell Experiment
10.13422/j.cnki.syfjx.20220214
- VernacularTitle:基于网络药理学和细胞实验探究心脉康片治疗动脉粥样硬化心血管病的作用机制
- Author:
Shu-ying ZHANG
1
;
Da-man CHEN
2
;
Xiao-han YE
1
Author Information
1. Dongguan Hospital， Guangzhou University of Chinese Medicine， Dongguan 523000， China
2. Fourth Clinical Medical College， Guangzhou University of Chinese Medicine， Shenzhen 518033， China
- Publication Type:Journal Article
- Keywords:
Xinmaikang tablets;
atherosclerosis cardiovascular disease;
mechanism of action;
network pharmacology;
cell experiment
- From:
Chinese Journal of Experimental Traditional Medical Formulae
2022;28(3):196-203
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveTo investigate the potential pharmacological mechanism of Xinmaikang tablets in the treatment of atherosclerosis cardiovascular disease by using network pharmacology and cell experimental validation. MethodThe components of Xinmaikang tablets were searched by BATMAN-TCM database and the active ingredients and potential targets were screened. The atherosclerosis related disease targets were searched in GeneCards and online mendelian inheritance in man（OMIM） disease databases. The therapeutic targets were obtained by mapping the intersection of the tablets and disease targets. Therapeutic targets were uploaded to STRING database to construct protein-protein interaction（PPI） network. Cytoscape software was used to create a "drug-active component-therapeutic target" network map， and a network topology algorithm was used to screen key action targets. David software was used for gene ontology（GO） and Kyoto encyclopedia of genes and genomes（KEGG） function enrichment analysis. The key targets of drug therapy were validated by in vitro cell assay. ResultA total of 19 active ingredients， 132 potential targets and 4703 atherosclerotic disease-related target genes of Xinmaikang tablets were retrieved and screened， and 84 intersection targets were obtained. 3 key therapeutic targets of Xinmaikang tablets in the treatment of atherosclerotic diseases were screened， including Calmodulin 1（CALM1）， voltage-dependent L-type calcium channel subunit alpha-1C（CACNA1C） and Phosphatidylinositol 4，5-bisphosphate 3-kinase catalytic subunit alpha isoform（PIK3CA）. A total of 313 biological processes， 89 molecular functions and 53 cell components were obtained by GO enrichment. A total of 40 pathways were obtained from KEGG functional enrichment， including purine metabolism， renin secretion， CGMP/PKG signaling pathway and so on. In vitro cell experiment results verified that Xinmaikang tablets can up-regulate the expression of CALM1 and CACNA1C， down-regulate the expression of PIK3CA， so as to inhibit the activity of inflammatory response， and play a therapeutic role in atherosclerotic diseases. ConclusionXinmaikang tablets may treat atherosclerosis cardiovascular disease through betulin， methyleugenol and other compounds， through purine metabolism， renin secretion， cGMP/PKG signaling pathway and other pathways， which acts on CALM1， CACNA1C， PIK3CA and other targets.
