کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2806275 1157112 2008 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Exercise training increases components of the c-Cbl–associated protein/c-Cbl signaling cascade in muscle of obese Zucker rats
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی علوم غدد
پیش نمایش صفحه اول مقاله
Exercise training increases components of the c-Cbl–associated protein/c-Cbl signaling cascade in muscle of obese Zucker rats
چکیده انگلیسی

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.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Metabolism - Volume 57, Issue 6, June 2008, Pages 858–866
نویسندگان
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