Inhibitory mechanism of caffeine on insulin-stimulated glucose uptake in adipose cells

被引:31
作者
Akiba, T
Yaguchi, K
Tsutsumi, K
Nishioka, T
Koyama, I
Nomura, M
Yokogawa, K
Moritani, S
Miyamoto, K [1 ]
机构
[1] Kanazawa Univ, Sch Med, Dept Hosp Pharm, Kanazawa, Ishikawa 9208641, Japan
[2] Akiba Hosp, Chiba 2891805, Japan
[3] Fukui Prefectural Univ, Fac Nursing & Welf, Dept Nursing, Fukui 9101195, Japan
关键词
adipocytes; glucose uptake; insulin; phosphatidylinositol; 3-kinase; Akt; GLUT4;
D O I
10.1016/j.bcp.2004.07.036
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Caffeine inhibits insulin-induced glucose uptake in rat adipocytes and also decreases insulin sensitivity, including whole-body glucose disposal and glucose uptake in skeletal muscle, during a euglycemic-hyperinsulinemic clamp in human. However, the mechanism by which caffeine decreases the insulin sensitivity is not still clear. We found that pre-treatment with caffeine inhibited the insulin-induced 2-deoxy-D-[1-H-3]glucose uptake in a concentration-dependent manner in mouse preadipose MC-3T3-G2/PA6 cells differentiated into mature adipose cells. Caffeine also suppressed insulin-induced GLUT4 translocation in the differentiated cells. Although caffeine did not alter insulin-induced activation of PI3K and protein kinase C-zeta (PKC), an isoform of atypical PKC, which is reported to have an important role in insulin-induced GLUT4 translocation, we found that insulin-induced phosphorylation and activation of Akt were blocked by pre-treatment with caffeine. Inhibition of insulin-induced 2-deoxy-D-[1-H-3]glucose uptake by caffeine was also observed in primary cultured brown adipocytes in a concentration-dependent manner. These results may, in part, explain the ability of caffeine to decrease insulin sensitivity. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1929 / 1937
页数:9
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