Peroxisome proliferator-activated receptor gamma transactivation-mediated potentiation of glucose uptake by Bai-Hu-Tang

被引:21
作者
Chen, Ching-Chu [1 ,2 ]
Hsiang, Chien-Yun [3 ]
Chiang, An-Na [4 ]
Lo, Hsin-Yi [5 ,6 ]
Li, Chia-Ing [7 ]
机构
[1] China Med Univ Hosp, Dept Med, Div Endocrinol & Metab, Taichung, Taiwan
[2] China Med Univ, Coll Chinese Med, Sch Chinese Med, Dept Endocrinol & Metab, Taichung, Taiwan
[3] China Med Univ, Sch Med, Dept Microbiol, Taichung, Taiwan
[4] Natl Yang Ming Univ, Inst Biochem & Mol Biol, Taipei 112, Taiwan
[5] China Med Univ Hosp, Dept Nucl Med, Taichung, Taiwan
[6] China Med Univ Hosp, PET Ctr, Taichung, Taiwan
[7] China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
关键词
herbs; Bai-Hu-Tang; 3T3-L1; adipocyte; PPAR gamma; glucose uptake;
D O I
10.1016/j.jep.2008.03.001
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: The molecular mechanism of a traditional hypoglycemic Chinese herbal formula. Aim of the study: To explore the glucose uptake effect as well as the mechanism(s) of action of Bai-Hu-Tang (BHT), a traditional Chinese herbal formula, composed of anemarrhena, gypsum, licorice and rice. Materials and methods: Differentiated 3T3-L1 adipocytes were treated with vehicle, insulin or insulin plus different concentrations of BHT. The 2-deoxy-[H-3] glucose uptake assay was performed to measure the amount of glucose uptake. To explore the mechanism(s) of glucose uptake of BHT, we used two insulin signaling transduction inhibitors, N-Acetyl-Leu-Leu-Norleu-al (ALLN), a calpain inhibitor, and LY 294002, a phosphatidylinositol (PI)3-kinase inhibitor, to test if the glucose uptake effect was mediated by the insulin signaling pathway. We then used Western blot analysis to re-confirm the result of the insulin signaling inhibition assay. Finally, reporter chimera assay of HuH-7 cells was used to measure the peroxisome proliferator-activated receptor gamma (PPAR gamma) activation by BHT. Results: BHT potentiated insulin-stimulated glucose uptake in 3T3-L1 adipocytes. The effect of BHT-stimulated glucose uptake was neither inhibited by ALLN nor by LY 294002. The protein expression of PI3 kinase pathway did not change after BHT stimulation. PPAR gamma activation was elevated by 67.7 +/- 32% (p < 0.05) in HuH-7 cells treated with 0.8 mu g/ml of BHT. Conclusions: BHT stimulated glucose uptake in 3T3-L1 adipocytes. This effect was via PPAR gamma activation rather than via the insulin signaling pathway. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:46 / 50
页数:5
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