Richard-Bulteau Hélène, Serrurier Bernard, Crassous Brigitte, Banzet Sébastien, Peinnequin André, Bigard Xavier, Koulmann Nathalie
Centre de Recherches du Service de Santé des Armées, La Tronche, France.
Am J Physiol Cell Physiol. 2008 Feb;294(2):C467-76. doi: 10.1152/ajpcell.00355.2007. Epub 2007 Dec 12.
The present study was designed to test the hypothesis that increasing physical activity by running exercise could favor the recovery of muscle mass after extensive injury and to determine the main molecular mechanisms involved. Left soleus muscles of female Wistar rats were degenerated by notexin injection before animals were assigned to either a sedentary group or an exercised group. Both regenerating and contralateral intact muscles from active and sedentary rats were removed 5, 7, 14, 21, 28 and 42 days after injury (n = 8 rats/group). Increasing contractile activity through running exercise during muscle regeneration ensured the full recovery of muscle mass and muscle cross-sectional area as soon as 21 days after injury, whereas muscle weight remained lower even 42 days postinjury in sedentary rats. Proliferator cell nuclear antigen and MyoD protein expression went on longer in active rats than in sedentary rats. Myogenin protein expression was higher in active animals than in sedentary animals 21 days postinjury. The Akt-mammalian target of rapamycin (mTOR) pathway was activated early during the regeneration process, with further increases of mTOR phosphorylation and its downstream effectors, eukaryotic initiation factor-4E-binding protein-1 and p70(s6k), in active rats compared with sedentary rats (days 7-14). The exercise-induced increase in mTOR phosphorylation, independently of Akt, was associated with decreased levels of phosphorylated AMP-activated protein kinase. Taken together, these results provided evidence that increasing contractile activity during muscle regeneration ensured early and full recovery of muscle mass and suggested that these beneficial effects may be due to a longer proliferative step of myogenic cells and activation of mTOR signaling, independently of Akt, during the maturation step of muscle regeneration.
通过跑步锻炼增加身体活动量有助于在广泛损伤后肌肉质量的恢复,并确定其中涉及的主要分子机制。在将雌性Wistar大鼠分为久坐组或运动组之前,通过注射蛇毒蛋白使大鼠左侧比目鱼肌发生退变。在损伤后5、7、14、21、28和42天,分别从活动组和久坐组大鼠中取出再生肌和对侧完整肌肉(每组n = 8只大鼠)。在肌肉再生过程中,通过跑步锻炼增加收缩活动,可确保在损伤后21天肌肉质量和肌肉横截面积完全恢复,而久坐组大鼠即使在损伤后42天肌肉重量仍较低。增殖细胞核抗原和MyoD蛋白表达在活动组大鼠中持续的时间比久坐组大鼠更长。损伤后21天,活动组动物的生肌调节因子蛋白表达高于久坐组动物。在再生过程早期,Akt-雷帕霉素哺乳动物靶蛋白(mTOR)信号通路被激活,与久坐组大鼠相比,活动组大鼠的mTOR磷酸化及其下游效应分子真核起始因子4E结合蛋白1和p70核糖体蛋白S6激酶进一步增加(第7 - 14天)。运动诱导的mTOR磷酸化增加独立于Akt,与磷酸化的AMP活化蛋白激酶水平降低有关。综上所述,这些结果表明,在肌肉再生过程中增加收缩活动可确保肌肉质量早期完全恢复,并提示这些有益作用可能归因于成肌细胞增殖步骤延长以及在肌肉再生成熟步骤中mTOR信号通路的激活(独立于Akt)。