Network pharmacology-based study on the mechanism of action of Trollius chinensis capsule in the treatment of upper respiratory tract infection

被引:0
|
作者
Wu, Jun [1 ]
Zhang, Hai-Ping [1 ]
Gao, Jing-Wen [1 ]
Liu, Zhi-Feng [1 ]
Jin, Lei [1 ]
机构
[1] Jianghan Univ, Hubei Peoples Hosp 3, Dept Gastroenterol, Wuhan 430000, Peoples R China
关键词
molecular docking; network pharmacology; Trollius chinensis; upper respiratory tract infection; IN-VITRO; BETA-SITOSTEROL; QUERCETIN; FLAVONOIDS; ACACETIN; INFLAMMATION; GALACTOSAMINE; DERIVATIVES; EXPRESSION; EXTRACT;
D O I
10.1097/MD.0000000000035529
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Upper respiratory tract infection (URTI), one of the most common respiratory diseases, has a high annual incidence. Trollius chinensis capsule has been used to treat URTI in China. However, the underlying-mechanisms remain unclear. Methods: Network pharmacology was used to explore the potential mechanism of action of Trollius chinensis capsule in URTI treatment. The active compounds in Trollius chinensis were obtained from the TCMSP, SymMap, and ETCM databases. The TCMSP, PubChem, and SwissTargetPrediction databases were used to predict potential targets of Trollius chinensis. URTI-associated targets were gathered from GeneCards and DisGeNET databases. The key targets and signaling pathways associated with URTI were selected by network topology, GO, and KEGG pathway enrichment analysis. Molecular docking was used to verify the binding activity between active compounds and key targets. Results: Quercetin, pectolinarigenin, beta-sitosterol, acacetin and cirsimaritin are major active compounds in Trollius chinensis capsule. Eighty one candidate therapeutic targets were confirmed to be involved in protection of Trollius chinensis capsule against URTI. Among them, 7 key targets (TP53, IL6, AKT1, CASP3, CXCL8, MMP9, and EGFR) were verified to have good binding affinities to the main active compounds. Furthermore, enrichment analyses suggested that inflammatory response, virus infection and oxidative stress related biological processes and pathways were possibly the potential mechanism. Conclusion: Overall, the present study clarified that quercetin, pectolinarigenin, beta-sitosterol, acacetin and cirsimaritin are proved to be the main effective compounds of Trollius chinensis capsule treating URTI, possibly by acting on the targets of IL6, AKT1, CASP3, CXCL8, MMP9 and EGFR to play anti-infectious, anti-viral, and anti-oxidative effects. This study provides a new understanding of the active compounds and mechanisms of Trollius chinensis capsule in URTI treatment from the perspective of network pharmacology.
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页数:16
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