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首页> 外文期刊>FEBS Open Bio >Decreased grip strength, muscle pain, and atrophy occur in rats following long‐term exposure to excessive repetitive motion
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Decreased grip strength, muscle pain, and atrophy occur in rats following long‐term exposure to excessive repetitive motion

机译:长期反复运动过多会导致大鼠握力下降,肌肉疼痛和萎缩

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Work‐related musculoskeletal disorders (WMSD) are caused by the overuse of muscles in the workplace. Performing repetitive tasks is a primary risk factor for the development of WMSD. Many workers in highly repetitive jobs exhibit muscle pain and decline in handgrip strength, yet the mechanisms underlying these dysfunctions are poorly understood. In our study, rats performed voluntary repetitive reaching and grasping tasks (Task group), while Control group rats did not perform these activities. In the Task group, grip strength and forearm flexor withdrawal threshold declined significantly from week 2 to week 6, compared with these values at week 0 (P 0.05). Relative muscle weight and muscle fiber cross‐sectional area of flexor digitorum superficialis (FDS) muscles decreased significantly in the Task group, compared with the Control group, at 6 weeks (P 0.05 and P 0.01, respectively). Nerve growth factor, glial cell line‐derived neurotrophic factor, and tumor necrosis factor α‐expression in FDS muscles were not significantly different in Control and Task groups at 3 and 6 weeks. At 6 weeks, the Task group had elevated MuRF1 protein levels (P = 0.065) and significant overexpression of the autophagy‐related (Atg) proteins, Beclin1 and Atg5–Atg12, compared with in the Control group (both P 0.05). These data suggested that long‐term exposure to excessive repetitive motion causes loss of grip strength, muscle pain, and skeletal muscle atrophy. Furthermore, this exposure may enhance protein degradation through both the ubiquitin‐proteasome and autophagy‐lysosome systems, thereby decreasing skeletal muscle mass.
机译:与工作相关的肌肉骨骼疾病(WMSD)是由工作场所过度使用肌肉引起的。执行重复性任务是开发WMSD的主要风险因素。许多从事高度重复性工作的工人表现出肌肉疼痛和握力下降,但对这些功能障碍的潜在机制了解甚少。在我们的研究中,大鼠执行了自愿的重复到达和抓握任务(任务组),而对照组大鼠则没有执行这些活动。在任务组中,与第0周时的这些值相比,从第2周到第6周时,握力和前臂屈肌缩回阈值显着下降(P 0.05)。与对照组相比,任务组在第6周时,浅指屈肌(FDS)的相对肌肉重量和肌纤维横截面积显着下降(分别为P 0.05和P 0.01)。对照组和任务组在3周和6周时,FDS肌肉中的神经生长因子,神经胶质细胞系衍生的神经营养因子和肿瘤坏死因子α表达没有显着差异。与对照组相比,任务组在第6周时的MuRF1蛋白水平升高(P = 0.065),并且自噬相关(Atg)蛋白Beclin1和Atg5–Atg12明显过表达(两者均为P 0.05)。这些数据表明,长期过度运动会导致握力下降,肌肉疼痛和骨骼肌萎缩。此外,这种暴露可能通过遍在蛋白-蛋白酶体和自噬-溶酶体系统增强蛋白质降解,从而减少骨骼肌质量。

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