Study on the mechanism of treating COVID-19 with Shenqi Wan based on network pharmacology

被引:11
|
作者
Ye, Xian-wen [1 ,2 ]
Deng, Ya-ling [1 ]
Zhang, Xia [1 ]
Liu, Min-min [1 ]
Liu, Ying [1 ]
Xie, Ya-ting [1 ]
Wan, Quan [1 ]
Huang, Min [1 ]
Zhang, Tao [1 ]
Xi, Jia-he [1 ]
Zhang, Jin-lian [1 ]
机构
[1] Jiangxi Univ Chinese Med, Sch Pharm, Nanchang 330006, Jiangxi, Peoples R China
[2] Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing Key Lab Qual Evaluat Chinese Mat Med, Beijing, Peoples R China
关键词
Shenqi Wan; novel coronavirus pneumonia; network pharmacology; mechanism; molecular docking; LUNG-CANCER CELLS; NF-KAPPA-B; CORONAVIRUS PNEUMONIA; DISEASE; EXPLORATION; ACTIVATION; APOPTOSIS; MIGRATION;
D O I
10.1080/03639045.2021.1989453
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Purpose Through the method of network pharmacology, the active components and targets of Shenqi Wan (SQW) were excavated, the relationship with novel Coronavirus pneumonia (COVID-19) was discussed, and the possible mechanism of SQW in the treatment of COVID-19 was revealed from the aspects of multicomponents, multitargets, and multipathways. Methods Firstly, the active components of SQW were screened from traditional Chinese medicine systems pharmacology database and analysis platform and the 2020 edition of Chinese Pharmacopeia, and the related targets of the components were obtained. Then the disease targets related to COVID-19 were screened from GeneCards and Online Mendelian Inheritance in Man. Venny was used to map the relationship between component-target and disease-target, and String was used to analyze the interaction of common targets. The network was constructed and analyzed by Cytoscape, the function of Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) genes was enriched by Metascape, and the molecular docking was verified by CB-Dock. Results Finally, 45 active components of SQW were obtained, and 72 potential targets were related to COVID-19, angiotensin-converting enzyme 2 (ACE2), interleukin (IL)-6, nitric oxide synthase (NOS3) and, C-reactive protein (CRP),may be the key targets. GO enrichment of 1715 projects, such as lipopolysaccharide stress response, active oxygen metabolism, positive regulation of cell migration, and other GO enrichment. About 136 KEGG pathways, tumor necrosis factor signaling pathway, IL-17 signaling pathway, hypoxia-inducible factor 1-alpha signaling pathway were obtained. Molecular docking showed that kaempferol, quercetin, luteolin, astragaloside, calyx isoflavone glucoside, matrine, and other COVID-19-related targets such as ACE2, chymotrypsin-like protease (3CLpro), papain-like protease (PLpro), prostaglandin-endoperoxide synthase 2 (PTGS2) have good binding ability. Conclusion According to the above results, it is suggested that SQW may play a role in the treatment of COVID-19 by directly or indirectly combining kaempferol, quercetin, and luteolin with ACE2, 3CLpro, PLpro, and PTGS2 to regulate multiple biological functions and signaling pathways.
引用
收藏
页码:1279 / 1289
页数:11
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