The influence of biological sex on the metabolic basis of skeletal muscle fatigue in vivo.

IF 4.4 2区 医学 Q1 NEUROSCIENCES
Fabio G Laginestra, Ryan M Broxterman, Danilo Iannetta, Matthew T Lewis, Jason S Kofoed, Jesse C Craig, Gregory Stoddard, Gwenael Layec, Eun-Kee Jeong, Markus Amann
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引用次数: 0

Abstract

This study in humans was designed to evaluate: (1) the overall relationships between muscle fatigue and inorganic phosphate (Pi) and hydrogen ions (H+) in women and men, and (2) whether the decline in contractile function for a given change in these intramuscular metabolites differs between sexes (i.e. muscle fatigue sensitivity). Sixteen healthy, young individuals (eight women) performed two consecutive (interspersed by 5 min of rest) intermittent isometric single-leg knee-extensor trials (60 maximal voluntary contractions; 3 s contraction, 2 s relaxation). Throughout both trials, intramuscular quadriceps [Pi] and [H+] were quantified using phosphorus magnetic resonance spectroscopy, and quadriceps twitch force (Qtw) was measured using electrical femoral nerve stimulation. The exercise-induced reduction in Qtw was greater in men than in women in both trials (both P < 0.048). In both sexes, the Qtw-[Pi] relationship was unchanged across trials, while the Qtw-[H+] relationship shifted downwards. The decline in Qtw for a given increase in [Pi] or [H+] was not different between men and women. The exercise-induced reduction in Qtw was strongly associated only with Pi accumulation (r = 0.761, P < 0.001). These results show that, in both sexes, Qtw is more consistently related to Pi than to H+, and that the decrease in Qtw for a given increase in [Pi] and [H+] does not differ between women and men. This supports that the in vivo metabolic basis of muscle fatigue is similar across sexes, and that differences in the exercise-induced reduction in contractile function relate to the extent of metabolic disturbance, rather than to an inherent fatigue resistance. KEY POINTS: The decline in muscle contractile function during high-intensity exercise (i.e. muscle fatigue) is generally less in women than in men. Sex-related differences in the intrinsic resistance to intramuscular metabolites may explain this divergence. We evaluated (1) the overall relationships between muscle fatigue and inorganic phosphate (Pi) and hydrogen ions (H+) in women and men, and (2) whether the decline in contractile function for a given change in intramuscular metabolites differs between sexes. In both sexes, intramuscular Pi was more consistently related to muscle fatigue compared with H+. For each metabolite (Pi or H+), the decrease in contractile function for a given intramuscular accumulation was similar in women and men. In conclusion, in vivo the metabolic basis of muscle fatigue is similar between sexes. Sex differences in the magnitude of fatigue are therefore probably not due to an intrinsic resistance to intramuscular metabolites.

生物性别对体内骨骼肌疲劳代谢基础的影响。
这项人体研究旨在评估:(1)女性和男性肌肉疲劳与无机磷酸盐(Pi)和氢离子(H+)之间的总体关系,以及(2)这些肌肉内代谢物的给定变化是否导致收缩功能的下降在性别之间存在差异(即肌肉疲劳敏感性)。16名健康的年轻人(8名女性)进行了两次连续(中间间隔5分钟休息)间歇等长单腿膝关节伸肌试验(60次最大自主收缩,3秒收缩,2秒放松)。在两项试验中,采用磷磁共振波谱法量化肌内股四头肌[Pi]和[H+],并采用股神经电刺激法测量股四头肌抽动力(Qtw)。在两项试验中,运动导致的Qtw降低在男性中都大于女性(ptw -[Pi]关系在两项试验中都没有变化,而Qtw-[H+]关系则向下移动。在给定的[Pi]或[H+]增加的情况下,Qtw的下降在男性和女性之间没有差异。运动引起的Qtw减少仅与Pi积累密切相关(r = 0.761), ptw与Pi的关系比与H+的关系更一致,并且在给定的[Pi]和[H+]增加的情况下,Qtw的减少在男女之间没有差异。这支持了肌肉疲劳的体内代谢基础在两性之间是相似的,运动引起的收缩功能减少的差异与代谢紊乱的程度有关,而不是与固有的疲劳抵抗有关。重点:在高强度运动中,肌肉收缩功能的下降(即肌肉疲劳)在女性中通常比在男性中少。对肌内代谢物内在抵抗力的性别差异可能解释了这种差异。我们评估了(1)女性和男性肌肉疲劳与无机磷酸盐(Pi)和氢离子(H+)之间的总体关系,以及(2)肌肉内代谢物变化导致的收缩功能下降是否因性别而异。在两性中,与H+相比,肌内Pi与肌肉疲劳的关系更为一致。对于每种代谢物(Pi或H+),给定肌肉内积累的收缩功能下降在女性和男性中是相似的。总之,体内肌肉疲劳的代谢基础在两性之间是相似的。因此,疲劳程度的性别差异可能不是由于对肌内代谢物的内在抵抗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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