Juškevičiūtė Ema, Neuberger Elmo W I, Eimantas Nerijus, Hoeter Katharina, Chang Yu-Kai, Simon Perikles, Brazaitis Marius
Institute of Sport Science and Innovations, Lithuanian Sports University, Kaunas, Lithuania.
Department of Sports Medicine, Disease Prevention and Rehabilitation, Johannes Gutenberg University Mainz, Mainz, Germany.
Eur J Appl Physiol. 2025 Jul 3. doi: 10.1007/s00421-025-05861-8.
Circulating cell-free DNA (cfDNA) is recognized as a relevant biomarker for monitoring the effects of various physiological and pathophysiological factors. To identify the effect of body temperature, we investigated the kinetics of cfDNA in response to two forms of heating.
In a randomized crossover design, twelve healthy young males cycled at 60% of their maximum oxygen uptake (VO) (exertional heating) and conducted lower-body immersion in hot water (43-44°C) (exogenous heating) until their rectal temperature (T) reached 39°C. EDTA blood samples were collected at each time point T increased and decreased by 0.5°C, to determine the concentrations of cfDNA, epinephrine (Epi), norepinephrine (NE), prolactin (PRL), as well as subjective sensation, and heart rate.
Linear mixed model analyses revealed a strong significant interaction effect for cfDNA (T × heating modality, F (6, 135.95) = 7.51, P < 0.001), with a significant 1.76-fold increase of cfDNA in response to exogenous heating and a 5.72-fold increase in response to exertional heating (P < 0.05). Significant interaction effects were detected for NE (F (6, 109.80) = 8.0683, P < 0.001), and PRL (F (6, 120.92) = 2.2746, P = 0.041), but not Epi. Repeated measures correlation (r) showed strong correlations between cfDNA and core temperature in exertional heating (r = 0.89), as well as exogenous heating (r = 0.75).
Our findings demonstrate that an increase in rectal temperature induces physiological stress, which triggers the release of cfDNA, however, at a significantly lower level than exertional heating, suggesting that mechanical stress has a greater influence on the release.
循环游离DNA(cfDNA)被认为是监测各种生理和病理生理因素影响的相关生物标志物。为了确定体温的影响,我们研究了cfDNA在两种加热形式下的动力学变化。
采用随机交叉设计,12名健康年轻男性以其最大摄氧量(VO)的60%进行骑行(运动性加热),并将下半身浸入热水(43 - 44°C)中(外源性加热),直至直肠温度(T)达到39°C。在T每次升高和降低0.5°C的每个时间点采集乙二胺四乙酸(EDTA)抗凝血样,以测定cfDNA、肾上腺素(Epi)、去甲肾上腺素(NE)、催乳素(PRL)的浓度,以及主观感觉和心率。
线性混合模型分析显示cfDNA存在显著的交互作用(T×加热方式,F(6, 135.95)=7.51,P<0.001),外源性加热使cfDNA显著增加1.76倍,运动性加热使其增加5.72倍(P<0.05)。NE(F(6, 109.80)=8.0683,P<0.001)和PRL(F(6, 120.92)=2.2746,P=0.041)存在显著交互作用,但Epi不存在。重复测量相关性(r)显示运动性加热(r=0.89)和外源性加热(r=0.75)时cfDNA与核心温度之间存在强相关性。
我们的研究结果表明,直肠温度升高会诱发生理应激,进而触发cfDNA的释放,然而,其释放水平显著低于运动性加热,这表明机械应激对释放的影响更大。