Laboratory of Muscle Biology and Sarcopenia, Division of Exercise Physiology, Department of Human Performance and Applied Exercise Science, West Virginia University School of Medicine , Morgantown, West Virginia.
Department of Physical Therapy, College of Health Professions and Department of Physiology, College of Medicine, University of Tennessee Health Sciences Center , Memphis, Tennessee.
J Appl Physiol (1985). 2018 Jun 1;124(6):1616-1628. doi: 10.1152/japplphysiol.00451.2017. Epub 2018 Feb 22.
Reloading of atrophied muscles after hindlimb suspension unloading (HSU) can induce injury and prolong recovery. Low-impact exercise, such as voluntary wheel running, has been identified as a nondamaging rehabilitation therapy in rodents, but its effects on muscle function, morphology, and satellite cell activity after HSU are unclear. This study tested the hypothesis that low-impact wheel running would increase satellite cell proliferation and improve recovery of muscle structure and function after HSU in mice. Young adult male and female C57BL/6 mice ( n = 6/group) were randomly placed into five groups. These included HSU without recovery (HSU), normal ambulatory recovery for 14 days after HSU (HSU+NoWR), and voluntary wheel running recovery for 14 days after HSU (HSU+WR). Two control groups were used: nonsuspended mouse cage controls (Control) and voluntary wheel running controls (ControlWR). Satellite cell activation was evaluated by providing mice 5-bromo-2'-deoxyuridine (BrdU) in their drinking water. As expected, HSU significantly reduced in vivo maximal force, decreased in vivo fatigability, and decreased type I and IIa myosin heavy chain (MHC) abundance in plantarflexor muscles. HSU+WR mice significantly improved plantarflexor fatigue resistance, increased type I and IIa MHC abundance, increased fiber cross-sectional area, and increased the percentage of type I and IIA muscle fibers in the gastrocnemius muscle. HSU+WR mice also had a significantly greater percentage of BrdU-positive and Pax 7-positive nuclei inside muscle fibers and a greater MyoD-to-Pax 7 protein ratio compared with HSU+NoWR mice. The mechanotransduction protein Yes-associated protein (YAP) was elevated with reloading after HSU, but HSU+WR mice had lower levels of the inactive phosphorylated YAP, which may have contributed to increased satellite cell activation with reloading after HSU. These results indicate that voluntary wheel running increased YAP signaling and satellite cell activity after HSU and this was associated with improved recovery. NEW & NOTEWORTHY Although satellite cell involvement in muscle remodeling has been challenged, the data in this study suggest that voluntary wheel running increased satellite cell activity and suppressed Yes-associated protein (YAP) protein relative to no wheel running and this was associated with improved muscle recovery of force, fatigue resistance, expression of type I myosin heavy chain, and greater fiber cross-sectional area after disuse.
去负荷(HSU)后萎缩肌肉的再负荷会导致损伤并延长恢复时间。低强度运动,如自愿轮跑,已被确定为啮齿动物非损伤性康复治疗方法,但它对 HSU 后肌肉功能、形态和卫星细胞活性的影响尚不清楚。本研究测试了以下假设:低强度轮跑会增加卫星细胞增殖,并改善 HSU 后小鼠肌肉结构和功能的恢复。年轻成年雄性和雌性 C57BL/6 小鼠(每组 6 只)被随机分为五组。这些组包括 HSU 无恢复(HSU)、HSU 后 14 天正常步行恢复(HSU+NoWR)和 HSU 后 14 天自愿轮跑恢复(HSU+WR)。还使用了两个对照组:未悬挂的小鼠笼对照(Control)和自愿轮跑对照(ControlWR)。通过向小鼠饮用水中提供 5-溴-2'-脱氧尿苷(BrdU)来评估卫星细胞激活。正如预期的那样,HSU 显著降低了体内最大力,降低了体内疲劳性,并降低了跖屈肌中 I 型和 IIa 肌球蛋白重链(MHC)的含量。HSU+WR 小鼠显著提高了跖屈肌抗疲劳能力,增加了 I 型和 IIa MHC 的含量,增加了纤维横截面积,并增加了比目鱼肌中 I 型和 IIA 肌纤维的百分比。与 HSU+NoWR 小鼠相比,HSU+WR 小鼠的肌纤维内 BrdU 阳性和 Pax7 阳性核的比例以及 MyoD 与 Pax7 蛋白的比值也显著增加。与 HSU 后再负荷相关的机械转导蛋白 Yes 相关蛋白(YAP)升高,但 HSU+WR 小鼠的非活性磷酸化 YAP 水平较低,这可能有助于 HSU 后再负荷时卫星细胞的激活增加。这些结果表明,自愿轮跑增加了 HSU 后 YAP 信号和卫星细胞活性,这与力的恢复、抗疲劳能力的提高、I 型肌球蛋白重链的表达以及失用后纤维横截面积的增加有关。