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Central and peripheral fatigue following non-exhaustive and exhaustive exercise of disparate metabolic demands

机译:不同代谢要求的非穷举和穷举运动后的中枢和周围疲劳

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The development of fatigue after non-exhaustive and exhaustive exercise eliciting differing metabolic demands is poorly understood. Sixteen active males completed five cycling trials. The first trial established the lactate threshold (LT) and maximal oxygen uptake (VO2max). Two of the remaining trials were completed at a severe intensity (halfway between LT and VO2max, SI) and two at a moderate intensity (90% LT, MI). Each trial involved two non-exhaustive bouts matched for work between intensities before cycling to exhaustion. Responses to stimulation of the femoral nerve and motor cortex were determined after each bout to determine peripheral and central fatigue. Corticospinal excitability, cortical silent period (cSP), short-interval intracortical inhibition (SICI), and intracortical facilitation (ICF) were also assessed. Non-exhaustive cycling induced greater peripheral and central fatigue in the SI compared with the MI (P<0.05). At exhaustion, there was no difference between intensities; however, peripheral fatigue tended to be greater in the SI vs MI (-31% vs -17%, respectively, P=0.051). Exhaustive cycling increased SICI (24%, P<0.001) and reduced the cSP (-14%, P<0.001) in the SI, whereas ICF was reduced in the MI (-16%, P<0.001). These findings demonstrate exercise-induced metabolic stress accelerates the development of peripheral and central fatigue, and differentially influences intracortical excitability.
机译:人们不十分了解在进行非穷举和穷举运动后会引起不同的代谢需求的疲劳。 16名活跃男性完成了5次自行车试验。首次试验确定了乳酸阈值(LT)和最大摄氧量(VO2max)。剩余的两项试验以高强度(LT和VO2max,SI之间的一半)完成,而两项试验以中等强度(LT,MI为90%)完成。每个试验都涉及两次非力竭性的运动,在骑自行车运动至力竭之前先进行两次强度不同的运动。每次发作后确定对股神经和运动皮层刺激的反应,以确定周围和中央疲劳。还评估了皮质脊髓兴奋性,皮质沉默期(cSP),短间隔皮质内抑制(SICI)和皮质内促进(ICF)。与MI相比,非穷举循环在SI中引起更大的外周和中央疲劳(P <0.05)。精疲力尽时,强度之间没有差异。但是,SI与MI的周围疲劳倾向更大(分别为-31%和-17%,P = 0.051)。力竭性循环增加SICI的SICI(24%,P <0.001),降低cSP(-14%,P <0.001),而MI的ICF降低(-16%,P <0.001)。这些发现表明,运动引起的代谢应激会加速周围和中央疲劳的发展,并差异地影响皮层内兴奋性。

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