Effects of Ji Tang Zhi on glucose metabolism and related protein expression in insulin resistance HepG 2 cell line
10.7501/j.issn.1674-6376.2017.06.010
- VernacularTitle:羁糖脂对HepG2胰岛素抵抗细胞葡萄糖代谢及相关蛋白表达的影响
- Author:
Minqiang YIN
;
Xi LIU
;
Tingting WU
;
Shenglai ZHANG
;
Yuyong DING
- Keywords:
Ji Tang Zhi;
Insulin resistance;
HepG2 cell line;
phosphorylation-Insulin Receptor Substrate 1 Serine 307,p-IRS-1 Ser307;
Phosphatidylinositol-3-Kinase (PI3K);
Glucose Transporter 4 (GLUT-4)
- From:
Drug Evaluation Research
2017;40(6):783-787
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate the effect of Ji Tang Zhi on glucose metabolism in insulin resistance (IR) HepG 2 cell line,and to explore the related mechanism.Methods The HepG2 cells were incubated in culture medium addition of 10-7 mol/L insulin for 24 h to establish the IR cell model.Effect of Ji Tang Zhi on rate of glucose absorption in HepG2 cell was detected by the method of glucose oxidase-peroxidase (GOD-POD).We performed an MTT assay to determine cytotoxicity effects of Ji Tang Zhi on HepG2 cell line.The expression of p-IRS-1 Ser307,PI3K and GLUT-4 were detected by Western blotting.Results Incubated with 10-7 mol/L insulin for 24 h,the insulin resistance cell model had been built.Compared with model group,the rate of glucose absorption of cell treated with JTZ (30 ～ 120 μg/mL) was significantly improved.According to model cells,the expression of GLUT-4 and PI3K decreased significantly compared to control cells.While the expression of p-IRS-1 Ser 307 was inhibited and GLUT-4 and PI3K expression were increased in IR cells after treated with JTZ (30 ～ 120 μtg/mL).Conclusion JTZ exert beneficial effects on hyperglycosemia in IR cell line possibly through regulating the levels of GLUT-4,p-IRS-1 Ser307 and PI3K in HepG2 cell.
