Uncovering the mechanism of Naoxintong capsule against hypertension based on network analysis and in vitro experiments

被引:0
|
作者
Chen, Xiatian [1 ]
Hu, Longgang [2 ]
Wang, Ruoying [3 ]
Luo, Min [1 ]
Wei, Chuang [1 ]
Li, Peifeng [1 ,4 ]
Yu, Hua [2 ,5 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Inst Translat Med, Qingdao, Peoples R China
[2] Qingdao Univ, Affiliated Cardiovasc Hosp, Qingdao, Peoples R China
[3] Lai Xi Hosp Tradit Chinese Med, Qingdao, Peoples R China
[4] Qingdao Univ, Affiliated Hosp, Inst Translat Med, 308 Ningxia Rd, Qingdao 266071, Peoples R China
[5] Qingdao Univ, Affiliated Cardiovasc Hosp, 1 Zhiquan Rd, Qingdao 266021, Peoples R China
基金
中国国家自然科学基金;
关键词
docking; hypertension; in vitro experiments; Naoxintong capsule; target prediction; OXIDATIVE STRESS; ATHEROSCLEROSIS; INFLAMMATION;
D O I
10.1111/cbdd.14440
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Naoxintong capsule (NXT) is a clinical drug for the treatment of cardiovascular diseases, but its pharmacological mechanism against hypertension remains unclear. Data concerning the compounds and targets of NXT were obtained from the TCMSP and DrugBank, whereas data concerning hypertension-related genes were obtained from DisGeNET. The network was analyzed and established by STRING and Cytoscape, and function enrichment was analyzed by GO and KEGG analysis. Molecular docking was performed to analyze the interaction between ingredients and targets, cellular activity was evaluated by MTT assay, and RT-qPCR and western blot were used to evaluate the expressions of related genes. The results showed that 146 active therapeutic components can target hypertension-related genes, and we found that core genes were mainly involved in the metabolism of lipids, lipopolysaccharides, the inflammatory signaling pathway, and the oxidative stress pathway. In addition, there was high affinity between the components of NXT and targets of hypertension, where the former can increase cell viability and reduce the expressions of NOX4, MCP-1, BAX, TNF-alpha and IL-1 beta. Moreover, NXT inhibited the expressions of IL-6 and Fis1, as well as increased the expression of MCL-1. These results revealed the active compounds, hypertension targets, signaling pathways, and molecular mechanisms of NXT for treating hypertension, offering references for the clinical application of NXT and the treatment of hypertension. We found that NXT played a function role in treating hypertension through the regulation of multi-targets, multi-channels and multi-components based on the network pharmacology and molecular docking. In addition, in vitro experiments validated that NXT can increase cell viability and reduce apoptosis and intracellular oxidative stress.image
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页数:10
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