Nedergaard A, Vissing K, Overgaard K, Kjaer M, Schjerling P
Institute of Sports Medicine, Bispebjerg Hospital, Copenhagen, Denmark.
J Appl Physiol (1985). 2007 Nov;103(5):1513-22. doi: 10.1152/japplphysiol.01445.2006. Epub 2007 Aug 9.
Unaccustomed exercise is known to produce strength loss, soreness, and myocellular disruption. With repeated application of exercise stimuli, the appearance of these indexes of muscle damage is attenuated, the so-called "repeated bout effect." No direct connection has been established between this repeated bout effect and exercise-induced increases in protein turnover, but it appears that a degree of tolerance is developed toward exercise for both. The present study sought to investigate markers of protein degradation by determining the expression of components related to the ubiquitin-proteasome system (UPS) with repeated exercise bouts. Healthy men carried out 30 min of bench stepping, performing eccentric work with one and concentric work with the other leg (n = 14), performing a duplicate exercise bout 8 wk later. A nonexercising control group was included (n = 6). RNA was extracted from muscle biopsies representing time points preexercise, +3 h, +24 h, and +7 days, and selected mRNA species were quantified using Northern blotting. The exercise model proved sufficient to produce a repeated bout effect in terms of strength and soreness. For forkhead box O transcription factor 1 (FOXO1) and muscle RING finger protein-1 (MURF1), strong upregulations were seen exclusively with concentric loading (P < 0.001), while atrogin-1 displayed a strong downregulation exclusively in response to eccentric exercise (P < 0.001). For MURF1 transcription, the first bout produced a downregulation that persisted until the second bout (P < 0.01). In conclusion, the UPS is modulated differentially in response to varying loading modalities and with different time frames in a way that to some extent reflects changes in protein metabolism known to take place with exercise.
众所周知,不习惯的运动会导致力量下降、酸痛和肌细胞破坏。随着运动刺激的反复施加,这些肌肉损伤指标的出现会减弱,即所谓的“重复运动效应”。这种重复运动效应与运动诱导的蛋白质周转增加之间尚未建立直接联系,但似乎对这两者都产生了一定程度的运动耐受性。本研究旨在通过确定与泛素 - 蛋白酶体系统(UPS)相关的成分在重复运动 bout 时的表达来研究蛋白质降解的标志物。健康男性进行了 30 分钟的台阶试验,一条腿进行离心运动,另一条腿进行向心运动(n = 14),8 周后重复进行相同的运动 bout。纳入了一个不运动的对照组(n = 6)。从代表运动前、运动后 +3 小时、+24 小时和 +7 天时间点的肌肉活检样本中提取 RNA,并使用 Northern 印迹法对选定的 mRNA 种类进行定量。该运动模型在力量和酸痛方面被证明足以产生重复运动效应。对于叉头框 O 转录因子 1(FOXO1)和肌肉环指蛋白 -1(MURF1),仅在向心负荷时观察到强烈上调(P < 0.001),而萎缩基因 1(atrogin -1)仅在响应离心运动时表现出强烈下调(P < 0.001)。对于 MURF1 转录,第一次 bout 产生的下调持续到第二次 bout(P < 0.01)。总之,UPS 根据不同的负荷方式和不同的时间框架进行差异调节,这种方式在一定程度上反映了已知运动时发生的蛋白质代谢变化。