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成纤维细胞生长因子-21改善胰岛素抵抗肝细胞对葡萄糖的吸收及机制

李婷婷 高丽昌 唐禄 张健 李富勇 李海燕 王晓杰 李校堃

中国药理学通报2012,Vol.28Issue(3):366-371,6.
中国药理学通报2012,Vol.28Issue(3):366-371,6.DOI:10.3969/j.issn.1001-1978.2012.03.016

成纤维细胞生长因子-21改善胰岛素抵抗肝细胞对葡萄糖的吸收及机制

The effect of FGF-21 on the glucose uptakes andinsulin resistance in cultured human liver cells

李婷婷 1高丽昌 2唐禄 1张健 2李富勇 3李海燕 1王晓杰 2李校堃2

作者信息

  • 1. 吉林农业大学生命科学学院,吉林,长春,130000
  • 2. 温州医学院药学院,浙江,温州,325035
  • 3. 浙江格鲁斯特生物科技有限公司,浙江,温州,325000
  • 折叠

摘要

Abstract

Aim To establish an insulin resistance cell model and evaluate the effects of FGF-21 on insulin resistance. Methods Human liver cells were administrated by high concentration of Dexamethasone and insulin. Glucose uptake activity of FGF-21 was examined by glucose oxidase and peroxidase( GOD-POD ) assay. The expressions of GLUT1 and the ERK1/2 signaling pathway were examined by Western blot. Results FGF-21 could stimulate glucose uptake of HL-7702 cells in a dose-dependent manner, suggesting that theglucose uptake assay was valid. Glucose uptake of HL-7702 cells stimulated by the mixture of FGF-21 and insulin was higher than that by FGF-21 or insulin solely. The FGF-21 protein was subsequently tested in IR cell models, showing that it could also stimulate glucose uptake of HL-7702 cells. The expressions of GLUT1 and the phosphorylation of ERK1/2 increased with the administration of FGF-21. The phosphorylation of ERK1/ 2 stimulated by FGF-21 was inhibited when PD98059, the specific inhibitor of ERK1/2, was added into thecell supernatant. In the IR model, FGF-21 could still increase the content of p-ERKl/2. Conclusions FGF-21 can stimulate glucose uptake of HL-7702 cells in a dose-dependent manner, and stimulate the glucose uptake of IR cell models. FGF-21 increases the ex-pression of GLUT1 and the phosphorylation of ERK1/2.

关键词

FGF-21/肝细胞/地塞米松/胰岛素抵抗/GLUT1/ERK1/2信号

Key words

FGF-21/ human liver cells/ dexametha- sone/ insulin resistance/ GLUT1/ ERK1/2 signaling pathway

分类

医药卫生

引用本文复制引用

李婷婷,高丽昌,唐禄,张健,李富勇,李海燕,王晓杰,李校堃..成纤维细胞生长因子-21改善胰岛素抵抗肝细胞对葡萄糖的吸收及机制[J].中国药理学通报,2012,28(3):366-371,6.

基金项目

国家科技重大专项"重大新药创制"(No 2011ZX09102-004-03) (No 2011ZX09102-004-03)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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