Department of Sports Medicine, Guangzhou Sports University, Guangzhou Dadao 1268, Guangzhou, 510076, China.
Eur J Appl Physiol. 2011 Nov;111(11):2743-52. doi: 10.1007/s00421-011-1892-5. Epub 2011 Mar 15.
Exercise improves high-fat diet (HFD)-induced skeletal muscle insulin resistance, but the mechanism is unresolved. This study aims to explore whether the improvement in response to exercise is associated with mTOR/S6K1 signaling and whether the signaling changes are muscle-specific. Male SD rats (150-180 g) were used for this study. After the experimental period, 6 weeks of exercise improved HFD-impaired intraperitoneal glucose tolerance and insulin-stimulated 2-deoxyglucose uptake in soleus (SOL) and extensor digitorum longus (EDL) muscles. Furthermore, 6 weeks of the HFD resulted in a reduced type I fiber ratio of SOL, an increased type I ratio of EDL, and a reduced fiber size of EDL, whereas exercise increased type I fiber ratio of SOL as well as type I fiber cross-sectional areas of EDL. However, the HFD had a main effect on basal cytosolic phosphorylation of S6K1 on Thr(389) content in SOL, which was also influenced by a significant interaction between the diet and exercise in EDL. Exercise had no direct effect on the basal phosphorylation of Akt on Ser(473), mTOR on Ser(2448), S6K1 on Thr(389) content in SOL. On the contrary, exercise prevented HFD-induced decrease in basal phosphorylation of S6K1 on Thr(389) content in EDL. These results indicate that 6 weeks of HFD and exercise lead to alterations in fiber type shift, fiber size, and basal phosphorylation of S6K1 on Thr(389) content in a muscle-specific pattern. Exercise prevents HFD-induced skeletal muscle insulin resistance, which is not associated with a reduced basal phosphorylation of mTOR/S6K1 alteration in the muscles.
运动可改善高脂肪饮食(HFD)诱导的骨骼肌胰岛素抵抗,但机制尚不清楚。本研究旨在探讨运动的改善是否与 mTOR/S6K1 信号有关,以及信号变化是否具有肌肉特异性。本研究使用雄性 SD 大鼠(150-180g)进行实验。经过实验期后,6 周的运动改善了 HFD 损害的腹腔内葡萄糖耐量和比目鱼肌(SOL)和伸趾长肌(EDL)肌肉中胰岛素刺激的 2-脱氧葡萄糖摄取。此外,6 周的 HFD 导致 SOL 的 I 型纤维比例降低,EDL 的 I 型比例增加,EDL 的纤维大小减小,而运动增加了 SOL 的 I 型纤维比例以及 EDL 的 I 型纤维横截面积。然而,HFD 对 SOL 中 S6K1 Thr(389) 含量的基础胞质磷酸化有主要影响,并且在 EDL 中还受到饮食和运动之间显著的相互作用的影响。运动对 Akt 的基础磷酸化 Ser(473)、mTOR 的基础磷酸化 Ser(2448)和 S6K1 的基础磷酸化 Thr(389)含量在 SOL 中没有直接影响。相反,运动防止了 HFD 诱导的 EDL 中 S6K1 的基础磷酸化 Thr(389)含量降低。这些结果表明,6 周的 HFD 和运动导致纤维类型转变、纤维大小以及 EDL 中 S6K1 的基础磷酸化 Thr(389)含量的改变具有肌肉特异性。运动可预防 HFD 诱导的骨骼肌胰岛素抵抗,这与肌肉中 mTOR/S6K1 基础磷酸化改变无关。