无论是否摄入酮酯,在缺氧环境中过一夜都会降低睡眠质量,但不会影响第二天的运动表现

Myrthe Stalmans, Domen Tominec, Ruben Robberechts, Wout Lauriks, Monique Ramaekers, Tadej Debevec, Chiel Poffe
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摘要

背景:在(模拟)高海拔地区睡觉在运动员中非常普遍,是高海拔训练营或体育比赛不可或缺的一部分。然而,人们也常常担心这会对睡眠质量产生负面影响,从而可能妨碍运动恢复和第二天的运动表现。我们最近的研究表明,摄入酮酯(KE)对在常氧状态下进行晚间剧烈运动后的睡眠有好处,并能缓解低氧血症。因此,我们假设摄入酮酯可能是减轻低氧血症引起的睡眠失调的有效策略。研究方法11名健康男性参与者完成了三个实验环节,包括常氧训练和随后在常氧或模拟海拔3000米处的睡眠,同时在运动后和睡眠前服用KE或安慰剂。睡眠情况通过多导睡眠监测仪进行评估,而第二天的运动表现则通过 30 分钟全力以赴计时赛(TT30)进行评估。生理测量包括血氧状态、心率变异性、通气参数、血液酸碱平衡和毛细血管血气。结果:缺氧导致睡眠效率下降约 3%,具体表现为睡眠开始后觉醒次数增加一倍,慢波睡眠减少约 22%。摄入 KE 缓解了整个前半夜 SpO2 的逐渐下降,但并没有改变缺氧引起的睡眠失调。KE和夜间缺氧都不会影响TT30的表现,但夜间缺氧会阻碍TT30后的心率恢复。结论我们观察到,在海拔 3,000 米的地方睡觉已经损害了睡眠效率。虽然这种缺氧引起的睡眠干扰过于微妙,不足以限制运动表现,但我们首次发现在高海拔地区睡眠会影响第二天的运动恢复。只要SpO2值低于约85%,KE就能缓解夜间低氧血症,但这并不能改善睡眠或第二天的运动表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A single night in hypoxia either with or without ketone ester ingestion reduces sleep quality without impacting next day exercise performance
Background: Sleeping at (simulated) altitude is highly common in athletes as an integral part of altitude training camps or sport competitions. However, it is also often feared due to proclaimed negative effects on sleep quality, thereby potentially hampering exercise recovery and next-day exercise performance. We recently showed that ketone ester (KE) ingestion beneficially impacted sleep following strenuous, late evening exercise in normoxia, and alleviated hypoxemia. Therefore, we hypothesized that KE ingestion may be an effective strategy to attenuate hypox(em)ia-induced sleep dysregulations. Methods: Eleven healthy, male participants completed three experimental sessions including normoxic training and subsequent sleep in normoxia or at a simulated altitude of 3,000m while receiving either KE or placebo post-exercise and pre-sleep. Sleep was evaluated using polysomnography, while next-day exercise performance was assessed through a 30-min all-out time trial (TT30). Physiological measurements included oxygen status, heart rate variability, ventilatory parameters, blood acid-base balance and capillary blood gases. Results: Hypoxia caused a ~3% drop in sleep efficiency, established through a doubled wakefulness after sleep onset and a ~22% reduction in slow wave sleep. KE ingestion alleviated the gradual drop in SpO2 throughout the first part of the night, but did not alter hypoxia-induced sleep dysregulations. Neither KE, nor nocturnal hypoxia affected TT30 performance, but nocturnal hypoxia hampered heart rate recovery following TT30. Conclusion: We observed that sleeping at 3,000m altitude already impairs sleep efficiency. Although this hypoxia-induced sleep disruption was too subtle to limit exercise performance, we for the first time indicate that sleeping at altitude impairs next-day exercise recovery. KE alleviated nocturnal hypoxemia whenever SpO2 values dropped below ~85%, but this did not translate into improved sleep or next-day exercise performance.
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