McCormick James J, King Kelli E, Goulet Nicholas, Carrillo Andres E, Fujii Naoto, Amano Tatsuro, Boulay Pierre, Kenny Glen P
Human and Environmental Physiology Research Unit, School of Human Kinetics, University of Ottawa, Ottawa, Ontario, Canada.
Department of Exercise Science, College of Health Sciences, Chatham University, Pittsburgh, Pennsylvania, United States.
Am J Physiol Regul Integr Comp Physiol. 2025 Mar 1;328(3):R289-R299. doi: 10.1152/ajpregu.00232.2024. Epub 2025 Feb 4.
Although activation of autophagy is vital for cellular survival during exposure to ambient heat and exercise, it remains unclear if autophagic activity differs between these heat stress conditions and if aging mediates this response. Young [ = 10, mean (SD): 22 (2) yr] and older males [ = 10, 70 (5) yr] performed 30 min of semi-recumbent cycling (70% maximal oxygen uptake). On a separate day, participants were immersed in warm water for 30 min, with the water temperature adjusted to induce the same increase in core temperature (rectal) as the prior exercise bout. Proteins associated with autophagy, inflammation, apoptosis, and the heat shock response (HSR) were assessed in peripheral blood mononuclear cells via Western blot before and after each exposure and during a 6-h seated recovery in a temperate environment (∼22°C). No differences in core temperature occurred at end-exposure to exercise or passive heating in either group (both, ≥ 0.999). Older adults exhibited greater autophagic regulation (significant LC3-II accumulation) to exercise when compared with passive heating at all time points (all, ≤ 0.022). However, passive heating alone may have impaired autophagy (elevated p62; = 0.044). Pro-inflammatory IL-6 was elevated during both conditions ( < 0.001) in older adults. Conversely, greater autophagic initiation (i.e., beclin-2) occurred in young adults at end-exercise and 3-h recovery when compared with passive heating (both, ≤ 0.024). The HSR and apoptotic responses were similar between conditions in both groups. Although brief exercise stimulates autophagy, exposure to ambient heat stress of an equivalent heat load may underlie autophagic dysregulation in older adults. We show that a short-duration (30-min) bout of vigorous-intensity exercise stimulates autophagy in young and older males when performed in a temperate environment. However, when exposed to an equivalent heat load as achieved during the prior exercise bout to elicit the same relative increase in core temperature via warm-water immersion, autophagic dysregulation occurs in older but not younger males.
尽管在暴露于环境热和运动期间自噬的激活对细胞存活至关重要,但尚不清楚在这些热应激条件下自噬活性是否存在差异,以及衰老是否介导了这种反应。年轻男性[ = 10,平均(标准差):22(2)岁]和老年男性[ = 10,70(5)岁]进行了30分钟的半卧位骑行(最大摄氧量的70%)。在另一天,参与者浸入温水中30分钟,水温经调整以诱导与先前运动回合相同的核心体温(直肠温度)升高。在每次暴露前后以及在温带环境(约22°C)中坐位恢复6小时期间,通过蛋白质印迹法在外周血单核细胞中评估与自噬、炎症、凋亡和热休克反应(HSR)相关的蛋白质。在两组中,运动或被动加热结束时核心体温均无差异(两者,≥ 0.999)。与所有时间点的被动加热相比,老年人在运动时表现出更大的自噬调节(显著的LC3-II积累)(所有,≤ 0.022)。然而,单独的被动加热可能损害了自噬(p62升高; = 0.044)。在两种情况下,老年人的促炎细胞因子IL-6均升高(< 0.001)。相反,与被动加热相比,年轻成年人在运动结束时和恢复3小时时发生了更大的自噬起始(即beclin-2)(两者,≤ 0.024)。两组中两种条件下的HSR和凋亡反应相似。尽管短暂运动刺激自噬,但暴露于等效热负荷的环境热应激可能是老年人自噬失调的基础。我们表明,在温带环境中进行的短时间(30分钟)高强度运动回合会刺激年轻和老年男性的自噬。然而,当暴露于与先前运动回合相同的热负荷下,通过温水浸泡引发相同的核心体温相对升高时,老年男性而非年轻男性会出现自噬失调。