Su Yan-Hong, Su Zhe, Zhang Kai, Yuan Qian-Kun, Liu Qiang, Lv Shen, Wang Zhao-Hui, Zou Wei
Physical Education College of Liaoning Normal University, Dalian 116029, China; Molecular Biology Lab, the Second Hospital of Dalian Medical University, Dalian 116029, China; College of Life Science of Liaoning Normal University, Dalian 116029, China.
Sheng Li Xue Bao. 2014 Oct 25;66(5):589-96.
This study was aimed to investigate the changes of muscle protein synthesis and degradation under different movement conditions, so as to provide theoretical basis for muscle atrophy mechanism. Sprague Dawley (SD) rats were randomly divided into control, endurance training (treadmill training), hind limb overhanging and eccentric training (treadmill training, angle -16º) groups. The gastrocnemius muscles of rats were taken and weighed. The muscle was sectioned, and HE staining was employed to determine the cell's cross-sectional area. Protein expression of p-Akt was measured by immunohistochemistry; and the expressions of MuRF1 and FoxO1 were determined by Western blot. The results showed that, compared with control group, hind limb overhanging and eccentric training groups exhibited decreased muscle weight and cross-sectional area, but endurance training group did not show any changes. The expressions of p-Akt in endurance and eccentric training groups, not in hind limb overhanging group, were significantly higher than that in control group. Compared with that of control, MuRF1 protein remained unchanged in endurance training groups, but was increased in eccentric training and hind limb overhanging groups; FoxO1 protein was decreased in endurance training group, but was increased in eccentric training and hind limb overhanging groups. These results indicate that movement (endurance and eccentric training) can activate Akt expression, but does not increase muscle weight, whereas eccentric training and hind limb overhanging can increase the expressions of MuRF1 and FoxO1, and induce amyotrophy, suggesting MuRF1 and FoxO1 are major determinant factors in muscle atrophy.
本研究旨在探讨不同运动条件下肌肉蛋白质合成与降解的变化,为肌肉萎缩机制提供理论依据。将Sprague Dawley(SD)大鼠随机分为对照组、耐力训练组(跑步机训练)、后肢悬吊组和离心训练组(跑步机训练,角度-16°)。取大鼠腓肠肌称重,将肌肉切片,采用苏木精-伊红(HE)染色测定细胞横截面积。采用免疫组织化学法检测p-Akt的蛋白表达;采用蛋白质免疫印迹法检测MuRF1和FoxO1的表达。结果显示,与对照组相比,后肢悬吊组和离心训练组的肌肉重量和横截面积减小,而耐力训练组无变化。耐力训练组和离心训练组p-Akt的表达显著高于对照组,后肢悬吊组则无显著变化。与对照组相比,耐力训练组MuRF1蛋白无变化,离心训练组和后肢悬吊组MuRF1蛋白增加;耐力训练组FoxO1蛋白减少,离心训练组和后肢悬吊组FoxO1蛋白增加。这些结果表明,运动(耐力训练和离心训练)可激活Akt表达,但不增加肌肉重量,而离心训练和后肢悬吊可增加MuRF1和FoxO1的表达,并诱导肌肉萎缩,提示MuRF1和FoxO1是肌肉萎缩的主要决定因素。