Elevated brain temperature under severe heat exposure impairs cortical motor activity and executive function

热疗 运动皮层 热应力 中暑 神经科学 医学 灌注 心理学 化学 内科学 生物 刺激 动物科学
作者
Xiang Ren Tan,Mary C. Stephenson,Sharifah Badriyah Alhadad,Kelvin Wei Zhern Loh,Tuck Wah Soong,Jason Lee,Ivan Cherh Chiet Low
出处
期刊:Journal of Sport and Health Science [Elsevier BV]
卷期号:13 (2): 233-244 被引量:27
标识
DOI:10.1016/j.jshs.2023.09.001
摘要

Excessive heat exposure can lead to hyperthermia in humans, which impairs physical performance and disrupts cognitive function. While heat is a known physiological stressor, it is unclear how severe heat stress affects brain physiology and function. Eleven healthy participants were subjected to heat stress from prolonged exercise or warm water immersion until their rectal temperatures (Tre) attained 39.5°C, inducing exertional or passive hyperthermia, respectively. In a separate trial, blended ice was ingested before and during exercise as a cooling strategy. Data were compared to a control condition with seated rest (normothermic). Brain temperature (Tbr), cerebral perfusion, and task-based brain activity were assessed using magnetic resonance imaging techniques. Tbr in motor cortex was found to be tightly regulated at rest (37.3°C ± 0.4°C) despite fluctuations in Tre. With the development of hyperthermia, Tbr increases and dovetails with the rising Tre. Bilateral motor cortical activity was suppressed during high-intensity plantarflexion tasks, implying a reduced central motor drive in hyperthermic participants (mean Tre: 38.5°C ± 0.1°C). Global gray matter perfusion and regional perfusion in sensorimotor cortex were reduced with passive hyperthermia. Executive function was poorer under a passive hyperthermic state, and this could relate to compromised visual processing as indicated by the reduced activation of left lateral-occipital cortex. Conversely, ingestion of blended ice before and during exercise alleviated the rise in both Tre and Tbr and mitigated heat-related neural perturbations. Severe heat exposure elevates Tbr, disrupts motor cortical activity and executive function, and this can lead to impairment of physical and cognitive performance.
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