Investigating the Active Substance and Mechanism of San-Jiu-Wei-Tai Granules via UPLC-QE-Orbitrap-MS and Network Pharmacology.

Autor:	Yu, Gengyuan, Zhang, Tonghua, Xu, Haoran, Bi, Yuelin, Feng, Xin, Wang, Jiaqi, Li, Tianyi, Zhang, Chenning, Sun, Yikun
Předmět:	INFLAMMATION prevention STOMACH tumors MEDICINAL plants HERBAL medicine HIGH performance liquid chromatography CHRONIC diseases ANTI-inflammatory agents EPIDERMAL growth factor receptors GASTRITIS HEAT shock proteins ORGANIC compounds DRUG resistance PHYTOCHEMICALS CELLULAR signal transduction MASS spectrometry TRANSFERASES PHARMACEUTICAL chemistry COMPUTER-assisted molecular modeling MOLECULAR structure MITOGEN-activated protein kinases CHINESE medicine PHARMACODYNAMICS CHEMICAL inhibitors
Zdroj:	Evidence-based Complementary & Alternative Medicine (eCAM); 10/17/2022, p1-26, 26p, 8 Diagrams, 2 Charts, 4 Graphs
Abstrakt:	San-Jiu-Wei-Tai granules (SJWTG) are a significant Chinese patent medicine for the treatment of chronic gastritis (CG), having outstanding advantages in long-term treatment; however, the chemical composition and potential mechanism have not been investigated until now. In this study, a rapid separation and identification method based on UPLC-QE-Orbitrap-MS was established, and 95 chemical components from SJWTGs were identified, including 6 chemical components of an unknown source that are not derived from the 8 herbs included in SJWTGs. The identified chemical components were subsequently analysed by network pharmacology, suggesting that the core targets for the treatment of CG with SJWTGs were EGFR, SRC, AKT1, HSP90AA1, MAPK1, and MAPK3 and thus indicating that SJWTGs could reduce the inflammatory response of gastric epithelial cells and prevent persistent chronic inflammation that induces cancerization by regulating the MAPK signalling pathway and the C-type lectin receptor signalling pathway as well as their upstream and downstream pathways in the treatment of CG. The key bioactive components in SJWTGs were identified as 2,6-bis(4-ethylphenyl)perhydro-1,3,5,7-tetraoxanaphth-4-ylethane-1,2-diol, a chemical component of an unknown source, murrangatin, meranzin hydrate, paeoniflorin, and albiflorin. The results of molecular docking showed the strong binding interaction between the key bioactive components and the core targets, demonstrating that the key bioactive components deserve to be further studied and considered as Q-markers. By acting on multiple targets, SJWTG is less susceptible to drug resistance during the long-term treatment of CG, indicating the advantage of Chinese patent medicines. Furthermore, the preventive effect of SJWTGs on gastric cancer also demonstrates the superiority of preventive treatment of disease with traditional Chinese medicine. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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