Analysis of the Composition and Anti-Rheumatoid Arthritis Mechanism of Qintengtongbi Decoction Based on Network Pharmacology

被引:2
作者
Liang, Guo-Cheng [1 ,2 ]
Duan, Wen-Gui [1 ]
Chen, Shu-Yin [2 ]
Fang, Jian-Kang [2 ]
机构
[1] Guangxi Univ, Sch Chem & Chem Engn, Nanning 530004, Guangxi Zhuang, Peoples R China
[2] Guangxi Univ Chinese Med, Ruikang Hosp, Nanning 530011, Guangxi Zhuang, Peoples R China
关键词
Qintengtongbi decoction (QTTBD); anti-rheumatoid arthritis; network pharmacology; component analysis; mechanism research; NF-KAPPA-B; EXPRESSION; PREDICTION; DISCOVERY; GENE; IL-6;
D O I
10.1177/1934578X211041421
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Qintengtongbi Decoction (QTTBD) is a traditional prescription for rheumatoid arthritis (RA) treatment in Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine, Nanning, southern China's Guangxi Zhuang Autonomous Region. However, there is not yet any analysis on its active compounds or action mechanism for treating RA. Moreover, the prescription has not been investigated from the perspective of network pharmacology. Therefore, this study aimed to analyze the compounds QTTBD and their potential pharmacological effects and the mechanism by which they treat RA via an integrated network pharmacology approach. With the aid of the relevant database tools and research indices, 188 compounds and 272 related drug targets genes/proteins were collected from QTTBD through the compound-target network, and 175 common gene targets between the QTTBD and RA were obtained by Venn 2.1. Finally, the top 10 gene targets and pathways were identified through the protein- protein interaction network, gene ontology, and KEGG pathway analysis: the gene targets include AKT1, IL6, TP53, VEGFA, MAPK3, TNF, CASP3, JUN, EGF, and EGFR; the pathways include oxytocin signaling pathway, amphetamine addiction, graft-versus-host disease, ovarian steroidogenesis, cGMP-PKG signaling pathway, Rap1 signaling pathway, allograft rejection, cytokine-cytokine receptor interaction, regulation of lipolysis in adipocytes and inflammatory mediator regulation of transient receptor potential channels. Therefore, it is concluded that a network pharmacology-based approach can help reveal and clarify the anti-RA role of QTTBD, and provide a scientific basis for further research into the mechanism.
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页数:13
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