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首页> 外文期刊>American Journal of Physiology >Physical Activity and Inactivity: Short-term intense exercise training reduces stress markers and alters the transcriptional response to exercise in skeletal muscle
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Physical Activity and Inactivity: Short-term intense exercise training reduces stress markers and alters the transcriptional response to exercise in skeletal muscle

机译:身体活动和不活动:短期激烈运动训练减少压力标记,并改变对骨骼肌运动的转录反应

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Hinkley JM, Konopka AR, Suer MK, Harber MP. Short-term intense exercise training reduces stress markers and alters the transcriptional response to exercise in skeletal muscle. Am J Physiol Regul Integr Comp Physiol 312: R426-R433, 2017. First published December 30, 2016; doi:10.1152/ajpregu.00356.2016 —The purpose of this investigation was to examine the influence of short-term intense endurance training on cycling performance, along with the acute and chronic signaling responses of skeletal muscle stress and stability markers. Ten recreationally active subjects (25 ± 2 yr, 79 ± 3 kg, 47 ± 2 ml-kg~-1.min~-1) were studied before and after a 12-day cycling protocol to examine the effects of short-term intense (70-100% Vo_2max) exercise training on resting and exercise-induced regulation of molecular factors related to skeletal muscle cellular stress and protein stability. Skeletal muscle biopsies were taken at rest and 3 h following a 20-km cycle time trial on days 1 and 12 to measure mRNA expression and protein content. Training improved (P < 0.05) cycling performance by 5 ± 1%. Protein oxidation was unaltered on day 12, while resting SAPK/JNK phosphorylation was reduced (P < 0.05), suggesting a reduction in cellular stress. The maintenance in the myocellular environment may be due to synthesis of cytoprotective markers, along with enhanced degradation of damage proteins, as training tended (P < 0.10) to increase resting protein content of manganese superoxide dismutase and heat shock protein 70 (HSP70), while mRNA expression of MuRF-1 was elevated (P < 0.05). Following training (day 12), the acute exercise-induced transcriptional response of TNF-alpha, NF-kappaB, MuRF-1, and PGC1alpha was attenuated (P < 0.05) compared with day 1. Collectively, these data suggest that short-term intense training enhances protein stability, creating a cellular environment capable of resistance to exercise-induced stress, which may be favorable for adaptation.
机译:Hinkley JM,Konopka Ar,Suer Mk,Harber MP。短期激烈运动训练减少了应力标记,并改变了在骨骼肌中运动的转录反应。 AM j Physiol Stead Intend Comp Physiol 312:R426-R433,20177。2016年12月30日第一次出版; DOI:10.1152 / AJPREGU.00356.2016-本调查的目的是研究短期强烈耐久性训练对循环性能的影响,以及骨骼肌胁迫和稳定标志物的急性和慢性信号响应。在12天的循环议定书之前和之后,研究了10个娱乐活动(25±2,79±3千克,47±2mL-kg〜-1.min〜-1),以检查短期激烈的影响(70-100%VO_2MAX)休息和运动诱导的骨骼肌细胞应激和蛋白质稳定性调节分子因子调节的运动培训。骨骼肌活组织检查在休息和3小时后,在20公里的循环时间试验后,在第1天和12时试验,以测量mRNA表达和蛋白质含量。培训改善(P <0.05)循环性能5±1%。蛋白质氧化在第12天内未置换,同时降低静息酸盐/ JNK磷酸化(P <0.05),表明细胞应激降低。肌细胞环境中的维护可能是由于细胞保护标记的合成,随着损伤蛋白的增强降解,随着培训(P <0.10)增加终氧化物歧化酶和热休克蛋白70(HSP70)的休息蛋白质含量(HSP70)而增加Murf-1的mRNA表达升高(P <0.05)。在培训(第12天)后,与第1天相比,衰减TNF-α,NF-κB,Murf-1和PGC1Alpha的急性运动诱导的转录响应(P <0.05),这些数据表明短期强烈的训练增强蛋白质稳定性,产生能够抵抗运动引起的应力的细胞环境,这可能有利于适应。

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