| Literature DB >> 29902887 |
Fang-Fang Fan1,2, Fei-Fei Guo2, Wen Zhang1,2, Yi Zhang2, Hong-Jun Yang2, Yi Zhang2, De-Feng Li2, Jing Zhang1, Jing-Jing Zhang2.
Abstract
In this study, a computer-based network pharmacology approach was applied to investigate the potential mechanism and important components of Rhodiola crenulata in the protection of H9c2 cells against hydrogen peroxide (H₂O₂)-induced oxidative stress. The intestinal absorption liquid of R. crenulata enhanced the cell viability, maintained cell morphology and inhibited cell apoptosis in the H₂O₂-induced oxidative stress in H9c2. Then, computer-based network pharmacology was used to analyze the relevant mechanism. A total of 133 oxidative stress-related compounds were screened out; and 26 of them occupied the top 20%, and all of the compounds enriched in 43 oxidative stress-related key targets. Finally, a "compound-target-pathway-function" network was constructed. Based on the analysis of the network pharmacology, R. crenulata protected H9c2 cells against H₂O₂-induced oxidative stress probably by affecting apoptosis-related processes, such as cell death, nitric oxide metabolism, oxidative stress, mitochondrial mechanism, redox process, redox-related enzyme activty and other oxidative stress-related process. And salidroside, ethyl gallate and catechins, which were the main components of R. crenulata, played an important role in this process. Therefore, the potential mechanism and important components of R. crenulata revealed the protective effect on oxidative stress. This study shows a multi-component, multi-target and overall regulation effect of R. crenulata on the oxidative stress, and provides a reliable reference for subsequent systematic experimental studies for the pharmacodynamic material foundation and mechanism of action R. crenulata. Copyright© by the Chinese Pharmaceutical Association.Entities:
Keywords: Rhodiola crenulata ; intestinal absorption solution ; mechanism ; network pharmacology ; oxidative stress ; pharmacodynamic substance
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Year: 2018 PMID: 29902887 DOI: 10.19540/j.cnki.cjcmm.20180125.011
Source DB: PubMed Journal: Zhongguo Zhong Yao Za Zhi ISSN: 1001-5302