Sundberg Christopher W, Hunter Sandra K, Bundle Matthew W
Biomechanics Laboratory, Departments of Health and Human Performance and Organismal Biology and Ecology, University of Montana, Missoula, Montana; and
Neuromuscular Physiology Laboratory, Department of Physical Therapy, Marquette University, Milwaukee, Wisconsin.
J Appl Physiol (1985). 2017 Jan 1;122(1):130-141. doi: 10.1152/japplphysiol.00468.2016. Epub 2016 Nov 17.
The durations that muscular force and power outputs can be sustained until failure fall predictably on an exponential decline between an individual's 3-s burst maximum to the maximum performance they can sustain aerobically. The exponential time constants describing these rates of performance loss are similar across individuals, suggesting that a common metabolically based mechanism governs muscle fatigue; however, these conclusions come from studies mainly on men. To test whether the same physiological understanding can be applied to women, we compared the performance-duration relationships and neuromuscular activity between seven men [23.3 ± 1.9 (SD) yr] and seven women (21.7 ± 1.8 yr) from multiple exhaustive bouts of cycle ergometry. Each subject performed trials to obtain the peak 3-s power output (P), the mechanical power at the aerobic maximum (P), and 11-14 constant-load bouts eliciting failure between 3 and 300 s. Collectively, men and women performed 180 exhaustive bouts spanning an ~6-fold range of power outputs (118-1116 W) and an ~35-fold range of trial durations (8-283 s). Men generated 66% greater P (956 ± 109 W vs. 632 ± 74 W) and 68% greater P (310 ± 47 W vs. 212 ± 15 W) than women. However, the metabolically based time constants describing the time course of performance loss were similar between men (0.020 ± 0.003/s) and women (0.021 ± 0.003/s). Additionally, the fatigue-induced increases in neuromuscular activity did not differ between the sexes when compared relative to the pedal forces at P These data suggest that muscle fatigue during short-duration dynamic exercise has a common metabolically based mechanism determined by the extent that ATP is resynthesized by anaerobic metabolism.
NEW & NOTEWORTHY: Although men and women differed considerably in their absolute cycling performances, there was no sex difference in the metabolically based exponential time constant that described the performance-duration relationship. Similarly, the fatigue-induced increases in neuromuscular activity were not different between the sexes when compared from a metabolic perspective. These data suggest that men and women have similar rate-limiting mechanisms for short-duration dynamic exercise that are determined by the extent the exercise is supported by anaerobic metabolism.
肌肉力量和功率输出在达到疲劳前能够持续的时间,在个体的3秒爆发最大值到其有氧条件下能够维持的最大表现之间呈可预测的指数下降。描述这些表现损失率的指数时间常数在个体间相似,这表明一种基于代谢的共同机制支配着肌肉疲劳;然而,这些结论主要来自对男性的研究。为了测试同样的生理学理解是否适用于女性,我们比较了7名男性[23.3±1.9(标准差)岁]和7名女性(21.7±1.8岁)在多次力竭性自行车测功试验中的表现-持续时间关系和神经肌肉活动。每个受试者进行试验以获得3秒峰值功率输出(P)、有氧最大值时的机械功率(P),以及11 - 14次在3至300秒之间引发疲劳的恒定负荷试验。总体而言,男性和女性共进行了180次力竭性试验,功率输出范围约为6倍(118 - 1116瓦),试验持续时间范围约为35倍(8 - 283秒)。男性产生的P比女性大66%(956±109瓦对632±74瓦),P比女性大68%(310±47瓦对212±15瓦)。然而,描述表现损失时间进程的基于代谢的时间常数在男性(0.020±0.003/秒)和女性(0.021±0.003/秒)之间相似。此外,当相对于P时的踏板力进行比较时,疲劳诱导的神经肌肉活动增加在性别之间没有差异。这些数据表明,在短时间动态运动中,肌肉疲劳有一个基于代谢的共同机制,该机制由无氧代谢重新合成ATP的程度决定。
尽管男性和女性在绝对骑行表现上有很大差异,但在描述表现-持续时间关系的基于代谢的指数时间常数上没有性别差异。同样,从代谢角度比较时,疲劳诱导的神经肌肉活动增加在性别之间也没有差异。这些数据表明,男性和女性在短时间动态运动中有相似的限速机制,该机制由运动由无氧代谢支持的程度决定。