期刊
JOURNAL OF APPLIED PHYSIOLOGY
卷 92, 期 2, 页码 736-744出版社
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00784.2001
关键词
phosphatidylinositol 3-kinase; insulin receptor substrate-1; glucose uptake; tyrosine phosphorylation
资金
- NIDDK NIH HHS [R01 DK-47936] Funding Source: Medline
Exercise training improves skeletal muscle insulin sensitivity in the obese Zucker rat. The purpose of this study was to investigate whether the improvement in insulin action in response to exercise training is associated with enhanced insulin receptor signaling. Obese Zucker rats were trained for 7 wk and studied by using the hindlimb-perfusion technique 24 h, 96 h, or 7 days after their last exercise training bout. Insulin-stimulated glucose uptake (traced with 2-deoxyglucose) was significantly reduced in untrained obese Zucker rats compared with lean controls (2.2 +/- 0.17 vs. 5.4 +/- 0.46 mumol . g(-1) . h(-1)). Glucose uptake was normalized 24 h after the last exercise bout (4.9 +/- 0.41 mumol . g(-1).h(-1)) and remained significantly elevated above the untrained obese Zucker rats for 7 days. However, exercise training did not increase insulin receptor or insulin receptor substrate-1 (IRS-1) tyrosine phosphorylation, phosphatidylinositol 3-kinase (PI3-kinase) activity associated with IRS-1 or tyrosine phosphorylated immunoprecipitates, or Akt serine phosphorylation. These results are consistent with the hypothesis that, in obese Zucker rats, adaptations occur during training that lead to improved insulin-stimulated muscle glucose uptake without affecting insulin receptor signaling through the PI3-kinase pathway.
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