Inhibiting effects of three components of Astragalus membranaceus on oxidative stress in Chang Liver cells.
- Author:
Jian LI
;
Lin HAN
;
Yu-fang MA
;
Yi-fan HUANG
- Publication Type:Journal Article
- MeSH:
Astragalus membranaceus;
chemistry;
Cells, Cultured;
Cytochrome P-450 CYP2E1;
metabolism;
Humans;
Isoflavones;
pharmacology;
Liver;
drug effects;
Oxidative Stress;
drug effects;
Reactive Oxygen Species;
metabolism;
Saponins;
pharmacology;
Triterpenes;
pharmacology
- From:
China Journal of Chinese Materia Medica
2015;40(2):318-323
- CountryChina
- Language:Chinese
-
Abstract:
The main objective of this research is to investigate the effects of astragaloside IV, calycosin separately glucoside, formononetin on oxidative stress in Chang Liver cells induced by H2O2. In the experiments, Chang Liver cells (a kind of normal human hepatocytes) were used as the research object, bifendate which has a clear hepatoprotective effect was used as the positive control drug, then the oxidative damage model of Chang Liver cells were established by H2O2. Cells were divided into six groups: blank control group, oxidative stress group, astragaloside IV group, calycosin separately glucoside group, formononetin group and positive control group. Then endogenous antioxidant system related indexes were detected by micro plate and colorimetric method; intracellular reactive oxygen species (ROS) were detected by DCFH-DA fluorescent probe; and the expressions of CYP2E1 were evaluated by liver microsomes, mRNA, and protein, respectively with spectrophotometry, Real-time PCR method, and Western blot technique. Results showed that H2O2 decreased antioxidant activity, and increased ROS level and expression of CYP2E1. The above oxidative stress status had been changed with protections of the three components of Astragalus membranaceus (compared with oxidative stress group, P < 0.05, P < 0.01), which taken as a whole had equivalent effects as the drug of positive control group( bifendate). Taken together, three Astragalus membranaceus ingredients all had significant or extremely significant inhibiting effects on oxidative damaged Chang Liver cells which were induced by H2O2, and the oxidative damage of Chang Liver cells had been relieved.
