Impact of acute caffeine intake on local tolerance to cold before and after total sleep deprivation.

IF 2.6 4区 医学 Q2 PHYSIOLOGY
Baptiste de Lorgeril, Pierre-Emmanuel Tardo-Dino, Cyprien Bourrilhon, Michael Quiquempoix, Catherine Drogou, Lise Mateo, Mégane Erblang, Philippe Colin, Pascal Van Beers, Mounir Chennaoui, Danielle Gomez-Merino, Fabien Sauvet
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Abstract

Total sleep deprivation (TSD) alters local cold tolerance and could thus increase the risk of cold injury. We evaluated the impact of acute caffeine intake, the main countermeasure to TSD-related deleterious effects, on local cold tolerance before and after TSD. Thirty-six healthy subjects underwent two TSD protocols (i.e., continuous wakefulness), with randomized crossover intake of acute caffeine or placebo (2.5 mg/kg) administered twice during wakefulness. Before and after 33 h of TSD, finger (index and annular) temperature and skin blood flow were assessed during cold-water immersion (CWI, 5°C, 20 min) followed by 20 min of rewarming in ambient air. We showed no significant effects of TSD on mean finger temperature during CWI in the placebo condition, but a significant reduction of the minimal temperature (8.86°C ± 0.35°C vs. 8.64°C ± 0.27°C, p = 0.02). During rewarming, we showed a reduction in temperature in the placebo condition (p = 0.02 for the mean temperature and p = 0.03 for the maximal) and an increase in the skin blood flow disparity between fingers at the four points of laser speckle rewarming measurements (p = 0.03). After TSD, acute caffeine intake (vs. placebo) increased mean (+2.11°C ± 0.21°C, p = 0.01) and minimal (+0.61°C ± 0.10°C, p = 0.02) finger temperatures during CWI, and improved rewarming after CWI (mean and maximal temperatures) (+2.28°C ± 0.08°C, p = 0.01, and +2.06°C ± 0.12°C, p = 0.02, respectively). Before TSD, acute caffeine intake significantly increased (vs. placebo) mean temperatures during CWI (p = 0.03) and reduced pain from the onset (p = 0.03) to the end of CWI (p = 0.02) and the first 2 min of rewarming (p = 0.04). There was also a significant main effect of habitual daily caffeine consumption on minimal finger temperatures during CWI, which decreased significantly between 0 and 600 mg consumption (R2 = -0.43, p = 0.01), independently of the effects of day (before and after TSD) and treatment (caffeine and placebo conditions). These findings suggest that acute caffeine intake could be a protective countermeasure to local cold tolerance, particularly during TSD. However, habitual daily caffeine consumption is a factor of individual variability that should be recorded during CWI protocols. Clinical trial NCT03859882.

在完全睡眠剥夺前后,急性咖啡因摄入对局部耐寒能力的影响。
完全睡眠剥夺(TSD)会改变局部耐寒性,从而增加冷伤的风险。我们评估了急性咖啡因摄入(TSD相关有害效应的主要对策)对TSD前后局部耐寒性的影响。36名健康受试者接受了两种创伤后应激障碍方案(即持续清醒),在清醒期间随机交叉摄入急性咖啡因或安慰剂(2.5 mg/kg)两次。在TSD 33小时前后,在冷水浸泡(CWI, 5°C, 20分钟)和环境空气中再加热20分钟期间,评估手指(食指和环指)温度和皮肤血流量。我们发现,在安慰剂条件下,TSD对CWI期间的平均手指温度没有显著影响,但显著降低了最低温度(8.86°C±0.35°C vs. 8.64°C±0.27°C, p = 0.02)。在复温期间,我们发现安慰剂条件下的温度降低(平均温度p = 0.02,最高温度p = 0.03),并且在激光散斑复温测量的四个点上手指之间的皮肤血流量差异增加(p = 0.03)。TSD后,急性咖啡因摄入(与安慰剂相比)增加了CWI期间的平均(+2.11°C±0.21°C, p = 0.01)和最低(+0.61°C±0.10°C, p = 0.02)手指温度,并改善了CWI后的再温(平均和最高温度)(+2.28°C±0.08°C, p = 0.01和+2.06°C±0.12°C, p = 0.02)。在TSD之前,急性咖啡因摄入显著增加(与安慰剂相比)CWI期间的平均体温(p = 0.03),从CWI开始(p = 0.03)到CWI结束(p = 0.02)和重新升温的前2分钟(p = 0.04)疼痛减轻(p = 0.04)。在CWI期间,习惯性每日摄入咖啡因对手指最低温度也有显著的主要影响,在摄入0到600毫克之间显著降低(R2 = -0.43, p = 0.01),独立于日(创伤后应激障碍前后)和治疗(咖啡因和安慰剂条件下)的影响。这些发现表明,急性咖啡因摄入可能是局部耐寒性的保护性对策,特别是在创伤后应激障碍期间。然而,习惯性的每日咖啡因摄入量是个体差异的一个因素,应该在CWI协议中记录。临床试验NCT03859882。
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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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