Fatiguing high-intensity intermittent exercise depresses maximal Na+-K+-ATPase activity in human skeletal muscle assessed using a novel NADH-coupled assay.

IF 2.9 4区 医学 Q2 PHYSIOLOGY
Jeppe F Vigh-Larsen, Sara M Frangos, Kristian Overgaard, Graham P Holloway, Magni Mohr
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Abstract

The Na+-K+-ATPase is a critical regulator of ion homeostasis during contraction, buffering interstitial K+ accumulation, which is linked to muscle fatigue during intense exercise. Within this context, we adopted a recently reported methodology to examine exercise-induced alterations in maximal Na+-K+-ATPase activity. Eighteen trained healthy young males completed a repeated high-intensity cycling protocol consisting of three periods (EX1-EX3) of intermittent exercise. Each period comprised 10 × 45-s cycling at ~ 105% Wmax and a repeated sprint test. Muscle biopsies were sampled at baseline and after EX3 for determination of maximal in vitro Na+-K+-ATPase activity. Blood was drawn after each period and in association with a 2-min cycling test at a standardized high intensity (~ 90% Wmax) performed before and after the session to assess plasma K+ accumulation. Further, a 5-h recovery period with the ingestion of carbohydrate or placebo supplementation was implemented to explore potential effects of carbohydrate availability before sampling a final biopsy and repeating all tests. A ~ 12% reduction in maximal Na+-K+-ATPase activity was demonstrated following EX3 compared to baseline (25.2 ± 3.9 vs. 22.4 ± 4.8 μmol·min-1·g-1 protein, P = 0.039), which was sustained at the recovery time point (~ 15% decrease compared to baseline to 21.6 ± 5.9 μmol·min-1·g-1 protein, P = 0.008). No significant effect of carbohydrate supplementation was observed on maximal Na+-K+-ATPase activity after recovery (P = 0.078). In conclusion, we demonstrate an exercise-induced depression of maximal Na+-K+-ATPase activity following high-intensity intermittent exercise, which was sustained during a 5-h recovery period and unrelated to carbohydrate availability under the present experimental conditions. This was shown using a novel NADH coupled assay and confirms previous findings using other methodological approaches.

使用新型 NADH 耦合测定法评估疲劳性高强度间歇运动对人体骨骼肌最大 Na+-K+-ATP 酶活性的抑制作用。
Na+-K+-ATP 酶是收缩过程中离子平衡的关键调节因子,可缓冲间质 K+ 的积累,而间质 K+ 的积累与剧烈运动时的肌肉疲劳有关。在此背景下,我们采用了最近报道的一种方法来研究运动诱导的最大 Na+-K+-ATP 酶活性的变化。18 名训练有素的健康年轻男性完成了一个重复的高强度自行车运动方案,该方案由三个间歇运动阶段(EX1-EX3)组成。每个阶段包括 10 × 45 秒、约 105% Wmax 的骑行和重复冲刺测试。在基线和 EX3 之后采集肌肉活检样本,以测定最大体外 Na+-K+-ATP 酶活性。在每个阶段结束后抽血,并在训练前后进行标准化高强度(约 90% Wmax)2 分钟自行车测试,以评估血浆 K+ 的积累。此外,在最后一次活检取样和重复所有测试之前,在摄入碳水化合物或安慰剂补充剂的情况下进行了 5 小时的恢复期,以探索碳水化合物可用性的潜在影响。与基线相比(25.2 ± 3.9 vs. 22.4 ± 4.8 μmol-min-1-g-1蛋白,P = 0.039),EX3后最大Na+-K+-ATP酶活性降低了约12%,这种情况在恢复期持续存在(与基线相比降低了约15%,为21.6 ± 5.9 μmol-min-1-g-1蛋白,P = 0.008)。补充碳水化合物对恢复后最大 Na+-K+-ATP 酶活性没有明显影响(P = 0.078)。总之,我们证明了高强度间歇运动后运动诱导的最大 Na+-K+-ATP 酶活性抑制,这种抑制在 5 小时的恢复期内持续存在,并且在目前的实验条件下与碳水化合物的供应无关。这是用一种新型的 NADH 偶联测定法显示的,并证实了之前用其他方法得出的结论。
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
CiteScore
8.80
自引率
2.20%
发文量
121
审稿时长
4-8 weeks
期刊介绍: Pflügers Archiv European Journal of Physiology publishes those results of original research that are seen as advancing the physiological sciences, especially those providing mechanistic insights into physiological functions at the molecular and cellular level, and clearly conveying a physiological message. Submissions are encouraged that deal with the evaluation of molecular and cellular mechanisms of disease, ideally resulting in translational research. Purely descriptive papers covering applied physiology or clinical papers will be excluded. Papers on methodological topics will be considered if they contribute to the development of novel tools for further investigation of (patho)physiological mechanisms.
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