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Attenuated activation of the unfolded protein response following exercise in skeletal muscle of older adults

机译:运动后老年人骨骼肌中未折叠的蛋白质反应的减弱激活

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摘要

Sarcopenia is linked with impaired adaptive responses to exercise in aging skeletal muscle. The unfolded protein response (UPR) is an important intramyocellular molecular response pathway that is activated by exercise. The influence of age on skeletal muscle adaptive UPR in response to exercise, and the relationship to other key exercise-responsive regulatory pathways is not well-understood. We evaluated age-related changes in transcriptional markers of UPR activation following a single bout of resistance exercise in 12 young (27 ± 5yrs) and 12 older (75 ± 5yrs) healthy men and women. At baseline, there were modest differences in expression of UPR-related genes in young and older adults. Following exercise, transcriptional markers of UPR pathway activation were attenuated in older adults compared to young based on specific salient UPR-related genes and gene set enrichment analysis. The coordination of post-exercise transcriptional patterns between the UPR pathway, p53/p21 axis of autophagy, and satellite cell differentiation were less evident in older compared to young adults. In conclusion, transcriptomic analysis revealed an age-related decline in the adaptive UPR transcriptional response following a single bout of exercise that could contribute to impaired exercise responsiveness with age.
机译:肌肉减少症与骨骼肌衰老的运动适应性反应受损有关。展开的蛋白质反应(UPR)是重要的肌内分子反应途径,可通过运动激活。年龄对骨骼肌适应性UPR响应运动的影响以及与其他关键的运动响应性调节途径之间的关系尚不清楚。我们评估了12例年轻(27±5岁)和12岁(75±5岁)健康男性和女性单次抵抗运动后,UPR激活转录标记物的年龄相关变化。基线时,年轻人和老年人中与UPR相关的基因表达存在适度差异。运动后,基于特定的显性UPR相关基因和基因集富集分析,与年轻人相比,老年人中UPR途径激活的转录标记减弱。与年轻人相比,老年人的UPR途径,p53 / p21自噬轴和卫星细胞分化之间的运动后转录模式之间的协调性较不明显。总之,转录组分析显示,单次运动后与年龄相关的适应性UPR转录反应下降,这可能会导致年龄的运动反应能力下降。

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