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运动训练增加肥胖Zucker大鼠肌肉中与c-Cbl相关蛋白/c-Cbl信号级联反应的组分。

Exercise training increases components of the c-Cbl-associated protein/c-Cbl signaling cascade in muscle of obese Zucker rats.

作者信息

Bernard Jeffrey R, Saito Misato, Liao Yi-Hung, Yaspelkis Ben B, Ivy John L

机构信息

Exercise Physiology and Metabolism Laboratory, Department of Kinesiology and Health Education, University of Texas at Austin, Austin, TX 78712, USA.

出版信息

Metabolism. 2008 Jun;57(6):858-66. doi: 10.1016/j.metabol.2008.01.035.

Abstract

The purpose of this investigation was to determine whether alterations in the c-Cbl-associated protein/c-Cbl pathway and/or p38-mitogen-activated protein kinase (p38 MAP kinase) were associated with improved skeletal muscle insulin responsiveness in exercise-trained obese Zucker rats. Obese Zucker rats ran 5 d/wk on a motorized treadmill for 90 minutes over a 7-week period. Age-matched obese Zucker rats (OB-SED) and their lean littermates (LN-SED) were obtained to serve as nontrained controls. Twenty-four (OB-EX-24 h) or 48 hours (OB-EX-48 h) after the last exercise bout, the trained rats were studied via the hind limb perfusion technique in the presence of insulin. Insulin-stimulated glucose uptake was significantly decreased across the skeletal muscle of OB-SED rats compared with LN-SED, but was normalized in the obese rats by 7 weeks of training. The insulin-stimulated plasma membrane protein concentrations of TC10 and glucose transporter 4 were reduced in the sedentary Zuckers, but both proteins were increased by the training protocol. Training did not increase insulin-stimulated p38 MAP kinase protein concentration, nor did it have an effect on insulin-stimulated p38 MAP kinase phosphorylation at the plasma membrane. These results suggest that skeletal muscle insulin resistance is associated with reduced expression of TC10 and that this deficiency can be corrected with exercise training.

摘要

本研究的目的是确定c-Cbl相关蛋白/c-Cbl途径和/或p38丝裂原活化蛋白激酶(p38 MAP激酶)的改变是否与运动训练的肥胖Zucker大鼠骨骼肌胰岛素反应性改善有关。肥胖Zucker大鼠在电动跑步机上每周跑5天,持续7周,每次90分钟。获取年龄匹配的肥胖Zucker大鼠(OB-SED)及其瘦的同窝仔鼠(LN-SED)作为未训练的对照。在最后一次运动后24小时(OB-EX-24 h)或48小时(OB-EX-48 h),在胰岛素存在的情况下,通过后肢灌注技术对训练的大鼠进行研究。与LN-SED相比,OB-SED大鼠骨骼肌中胰岛素刺激的葡萄糖摄取显著降低,但肥胖大鼠经过7周训练后恢复正常。久坐不动的Zucker大鼠中,胰岛素刺激的TC-10和葡萄糖转运蛋白4的质膜蛋白浓度降低,但训练方案使这两种蛋白均增加。训练并未增加胰岛素刺激的p38 MAP激酶蛋白浓度,对质膜上胰岛素刺激的p38 MAP激酶磷酸化也无影响。这些结果表明,骨骼肌胰岛素抵抗与TC-10表达降低有关,且这种缺陷可通过运动训练得到纠正。

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