Brozinick J T, Etgen G J, Yaspelkis B B, Ivy J L
Department of Kinesiology, University of Texas at Austin 78712.
Am J Physiol. 1994 Jul;267(1 Pt 2):R236-43. doi: 10.1152/ajpregu.1994.267.1.R236.
The rates of muscle glucose uptake of lean and obese Zucker rats were assessed by hindlimb perfusion under basal conditions (no insulin), in the presence of a maximally stimulating concentration of insulin (10 mU/ml), and after muscle contraction elicited by electrical stimulation of the sciatic nerve. After perfusion, plasma and microsomal membranes were isolated from selected hindlimb muscles for determination of GLUT-4 protein distribution. Under basal conditions, rates of glucose uptake were similar for lean and obese rats despite plasma membranes from lean rats containing 82% more GLUT-4 protein than obese rats. Insulin stimulation resulted in significant increases in plasma membrane GLUT-4 protein concentration in lean but not obese rats. Glucose uptake of lean rats (35.3 +/- 4.7 mumol.h-1.g-1) in the presence of insulin was approximately fourfold greater than that of obese rats (8.8 +/- 1.3 mumol.h-1.g-1), but this difference in glucose uptake could not be completely accounted for by the difference in plasma membrane GLUT-4 protein concentration. Stimulation by contraction resulted in significant increases in plasma membrane GLUT-4 protein concentration in both lean and obese rats and similar rates of glucose uptake. These results suggest that the muscle insulin resistance of the obese Zucker rat is due to 1) a reduced plasma membrane GLUT-4 protein concentration, which results in part from an impairment in the insulin-stimulated GLUT-4 protein translocation process, and 2) a defect in the insulin-stimulated activation of this protein. However, contraction-stimulated glucose uptake, GLUT-4 protein translocation, and activation are normal in the obese Zucker rat.
在基础条件下(无胰岛素)、存在最大刺激浓度胰岛素(10 mU/ml)时以及通过电刺激坐骨神经引发肌肉收缩后,通过后肢灌注评估瘦型和肥胖型 Zucker 大鼠的肌肉葡萄糖摄取率。灌注后,从选定的后肢肌肉中分离出血浆和微粒体膜,以测定 GLUT-4 蛋白分布。在基础条件下,尽管瘦型大鼠的质膜中 GLUT-4 蛋白含量比肥胖型大鼠多 82%,但瘦型和肥胖型大鼠的葡萄糖摄取率相似。胰岛素刺激导致瘦型大鼠而非肥胖型大鼠的质膜 GLUT-4 蛋白浓度显著增加。存在胰岛素时,瘦型大鼠的葡萄糖摄取量(35.3±4.7 μmol·h⁻¹·g⁻¹)约为肥胖型大鼠(8.8±1.3 μmol·h⁻¹·g⁻¹)的四倍,但这种葡萄糖摄取差异不能完全由质膜 GLUT-4 蛋白浓度差异来解释。收缩刺激导致瘦型和肥胖型大鼠的质膜 GLUT-4 蛋白浓度显著增加,且葡萄糖摄取率相似。这些结果表明,肥胖型 Zucker 大鼠的肌肉胰岛素抵抗归因于:1)质膜 GLUT-4 蛋白浓度降低,这部分是由于胰岛素刺激的 GLUT-4 蛋白转位过程受损;2)胰岛素刺激该蛋白激活存在缺陷。然而,肥胖型 Zucker 大鼠中收缩刺激的葡萄糖摄取、GLUT-4 蛋白转位和激活是正常的。