Human Performance Laboratory, São Paulo State University, Rio Claro, SP, Brazil.
Department of Internal Medicine, University of Utah, Salt Lake City, UT, USA.
Exp Physiol. 2020 Dec;105(12):2073-2085. doi: 10.1113/EP088910. Epub 2020 Oct 18.
What is the central question of this study? Does creatine supplementation augment the total torque impulse accumulated above end-test torque (IET) during severe-intensity knee-extensor exercise by attenuating the rate of decrease in peak potentiated twitch torque (PT)? What is the main finding and its importance? Creatine augmented the IET and attenuated the rate of decrease in both voluntary activation and PT during severe-intensity exercise. The IET was related to the rate of decrease in PT. These findings reveal an important role for the rates of neuromuscular fatigue development as key determinants of exercise tolerance within the severe domain.
This study investigated the effect of creatine supplementation on exercise tolerance, total torque impulse accumulated above end-test torque (total IET) and neuromuscular fatigue development of the knee extensors during severe-intensity intermittent isometric exercise. Sixteen men were randomly allocated into Creatine (n = 8, 20 g day for 5 days) or Placebo (n = 8) groups and performed knee-extensor maximal voluntary contraction (MVC) testing, all-out testing to determine end-test torque (ET) and the finite torque impulse accumulated above end-test torque (IET'), and three submaximal tests at ET + 10%: (i) time to task failure without supplementation (Baseline); (ii) time to task failure after creatine or placebo supplementation; and (iii) time matched to Baseline after creatine (Creatine-Isotime) or placebo (Placebo-Isotime) supplementation. Creatine supplementation significantly increased the time to task failure (Baseline = 572 ± 144 s versus Creatine = 833 ± 221 s) and total IET (Baseline = 5761 ± 1710 N m s versus Creatine = 7878 ± 1903 N m s), but there were no significant differences within the Placebo group. The percentage change pre- to postexercise in MVC, voluntary activation, peak potentiated twitch torque and integrated EMG during MVC were not significantly different between Baseline and Creatine but were all significantly attenuated in Creatine-Isotime compared with Baseline. There were no significant differences in these variables within the placebo group. The total IET was significantly correlated with the rates of change in potentiated twitch torque peak (r = 0.83-0.87) and rate of torque development (r = -0.83 to -0.87) for the submaximal tests to task failure. These findings reveal an important role for the rates of neuromuscular fatigue development as key determinants of exercise tolerance during severe-intensity intermittent isometric exercise.
本研究的核心问题是什么?补充肌酸是否通过减弱峰值增强 twitch 扭矩 (PT) 的下降率来增加严重强度膝关节伸肌运动后积累的总扭矩脉冲 (IET)?主要发现及其重要性是什么?肌酸增加了 IET,并减弱了严重强度运动中自愿激活和 PT 的下降率。IET 与 PT 的下降率有关。这些发现揭示了神经肌肉疲劳发展速度作为严重运动耐受的关键决定因素的重要作用。
本研究旨在探讨肌酸补充对严重强度间歇性等长运动中膝关节伸肌耐力、运动后积累的总扭矩脉冲 (IET) 和神经肌肉疲劳发展的影响。16 名男性被随机分配到肌酸 (n=8,5 天 20 克/天) 或安慰剂 (n=8) 组,并进行膝关节伸肌最大自主收缩 (MVC) 测试、全力测试以确定运动后扭矩 (ET) 和运动后积累的有限扭矩脉冲 (IET'),以及 ET+10% 的三个亚最大测试:(i) 无补充时任务失败的时间 (基础期);(ii) 肌酸或安慰剂补充后任务失败的时间;(iii) 与基础期匹配的时间后肌酸 (肌酸-Isotime) 或安慰剂 (安慰剂-Isotime) 补充。肌酸补充显著增加了任务失败的时间 (基础期=572±144 s 与肌酸=833±221 s) 和总 IET (基础期=5761±1710 N·m·s 与肌酸=7878±1903 N·m·s),但安慰剂组无显著差异。基础期和肌酸之间,MVC 前至后、自愿激活、峰值增强 twitch 扭矩和 MVC 期间的集成 EMG 的变化百分比没有显著差异,但在肌酸-Isotime 中均显著低于基础期。安慰剂组这些变量无显著差异。总 IET 与亚最大运动至失败测试中增强 twitch 扭矩峰值的变化率 (r=0.83-0.87) 和扭矩发展率 (r=-0.83 至-0.87) 呈显著相关。这些发现揭示了神经肌肉疲劳发展速度作为严重强度间歇性等长运动中耐力的关键决定因素的重要作用。