Force transfer is integral for maintain'/> Alterations in the muscle force transfer apparatus in aged rats during unloading and reloading: impact of microRNA‐31
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Alterations in the muscle force transfer apparatus in aged rats during unloading and reloading: impact of microRNA‐31

机译:装卸过程中老年大鼠肌肉力量传递装置的变化:microRNA‐31的影响

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摘要

Key points class="unordered" style="list-style-type:disc" id="tjp13004-list-0001">Force transfer is integral for maintaining skeletal muscle structure and function. One important component is dystrophin. There is limited understanding of how force transfer is impacted by age and loading.Here, we investigate the force transfer apparatus in muscles of adult and old rats exposed to periods of disuse and reloading.Our results demonstrate an increase in dystrophin protein during the reloading phase in the adult tibialis anterior muscle that is delayed in the old muscle. The consequence of this delay is an increased susceptibility towards contraction‐induced muscle injury.Central to the lack of dystrophin protein is an increase in miR‐31, a microRNA that inhibits dystrophin translation. In vivo electroporation with a miR‐31 sponge led to increased dystrophin protein and decreased contraction‐induced muscle injury in old skeletal muscle.Overall, our results detail the importance of the force transfer apparatus and provide new mechanisms for contraction‐induced injury in ageing skeletal muscle.
机译:关键点 class =“ unordered” style =“ list-style-type:disc” id =“ tjp13004-list-0001”> <!-list-behavior = unordered prefix-word = mark-type = disc max- label-size = 0-> 力传递对于维持骨骼肌的结构和功能是必不可少的。肌营养不良蛋白是重要成分之一。关于力传递如何受年龄和负荷影响的理解还很有限。 在这里,我们研究了成年和成年大鼠在停用和再加载时期中肌肉中的力传递装置。 < li>我们的研究结果表明,成年胫骨前肌在重装阶段肌营养不良蛋白增加,而旧肌延迟。这种延迟的结果是增加了对收缩引起的肌肉损伤的敏感性。 缺乏肌营养不良蛋白的主要原因是miR-31的增加,这是一种抑制肌营养不良蛋白翻译的microRNA。使用miR‐31海绵进行体内电穿孔可导致肌营养不良蛋白增加,并减少旧骨骼肌的收缩性肌肉损伤。 总体而言,我们的结果详细说明了力传递装置的重要性,并提供了新的机制收缩引起的骨骼肌衰老损伤。

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