Heart E, Choi W S, Sung C K
Department of Physiology and Biophysics, University of Southern California, School of Medicine, Los Angeles, California 90033, USA.
Am J Physiol Endocrinol Metab. 2000 Jan;278(1):E103-12. doi: 10.1152/ajpendo.2000.278.1.E103.
To study molecular mechanisms for glucosamine-induced insulin resistance, we induced complete and reversible insulin resistance in 3T3-L1 adipocytes with glucosamine in a dose- and time-dependent manner (maximal effects at 50 mM glucosamine after 6 h). In these cells, glucosamine impaired insulin-stimulated GLUT-4 translocation. Glucosamine (6 h) did not affect insulin-stimulated tyrosine phosphorylation of the insulin receptor and insulin receptor substrate-1 and -2 and weakly, if at all, impaired insulin stimulation of phosphatidylinositol 3-kinase. Glucosamine, however, severely impaired insulin stimulation of Akt. Inhibition of insulin-stimulated glucose transport was correlated with that of Akt activity. In these cells, glucosamine also inhibited insulin stimulation of p70 S6 kinase. Glucosamine did not alter basal glucose transport and insulin stimulation of GLUT-1 translocation and mitogen-activated protein kinase. In summary, glucosamine induced complete and reversible insulin resistance in 3T3-L1 adipocytes. This insulin resistance was accompanied by impaired insulin stimulation of GLUT-4 translocation and Akt activity, without significant impairment of upstream molecules in insulin-signaling pathway.
为研究氨基葡萄糖诱导胰岛素抵抗的分子机制,我们用氨基葡萄糖以剂量和时间依赖性方式(6小时后50 mM氨基葡萄糖时达到最大效应)在3T3-L1脂肪细胞中诱导出完全可逆的胰岛素抵抗。在这些细胞中,氨基葡萄糖损害胰岛素刺激的葡萄糖转运蛋白4(GLUT-4)转位。氨基葡萄糖(6小时)不影响胰岛素刺激的胰岛素受体及胰岛素受体底物-1和-2的酪氨酸磷酸化,并且对胰岛素刺激的磷脂酰肌醇3激酶的损害很轻微(如果有的话)。然而,氨基葡萄糖严重损害胰岛素对Akt的刺激。胰岛素刺激的葡萄糖转运抑制与Akt活性抑制相关。在这些细胞中,氨基葡萄糖还抑制胰岛素对p70 S6激酶的刺激。氨基葡萄糖不改变基础葡萄糖转运以及胰岛素对葡萄糖转运蛋白1(GLUT-1)转位和丝裂原活化蛋白激酶的刺激。总之,氨基葡萄糖在3T3-L1脂肪细胞中诱导出完全可逆的胰岛素抵抗。这种胰岛素抵抗伴随着胰岛素刺激的GLUT-4转位和Akt活性受损,而胰岛素信号通路中的上游分子无明显损害。