Department of Neurobehavioral Genetics, Institute of Psychobiology, University of Trier, D-54290, Trier, Germany.
Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, D-68159, Mannheim, Germany.
Psychoneuroendocrinology. 2019 Apr;102:63-67. doi: 10.1016/j.psyneuen.2018.11.033. Epub 2018 Nov 30.
Secretion of the stress hormone cortisol follows a circadian rhythm and is stimulated following stress exposure. Cortisol regulates the transcription of several genes, primarily through activation of the glucocorticoid receptor (GR). Previously, we showed an upregulation of PERIOD genes PER1 and PER3 after pharmacological/glucocorticoid challenge in vivo and in vitro. The current study aims to investigate the temporal association between unstimulated, diurnal cortisol secretion and the expression of selected GR-target genes (PER1, PER2, PER3, FKBP5, GILZ and SDPR) in vivo to determine the timing of the most pronounced coupling between cortisol and mRNA expression. Unstimulated plasma and saliva cortisol concentrations and gene expression levels in whole blood were measured every 15 min from early morning until 16:00 h in 18 healthy men. Time-lagged correlations of cortisol concentrations with mRNA expression levels were assessed allowing lags between -240 and + 240 min. Strong positive correlations at non-zero lags between cortisol levels and the expression of FKBP5 (plasma: r = 0.74 (CI = 0.65-0.81), p < 0.001, lag + 90 min; saliva: r = 0.71 (CI = 0.61-0.78), p < 0.001, lag + 75 min), and GILZ (plasma: r = 0.59 (CI = 0.46-0.69), p < 0.001, lag + 30 min; saliva r = 0.53 (CI = 0.41-0.63), p < 0.001, lag +15 min) were observed. Expressions of PERIOD genes and SDPR correlated only weakly with cortisol (all |r| < 0.25). Our findings demonstrate strong correlations between cortisol secretion and gene expression in humans under unstimulated conditions. The observed time-lags can guide future research aiming to characterize glucocorticoid-dependent gene expression in clinical samples with stress-related disorders.
应激激素皮质醇的分泌遵循昼夜节律,在应激暴露后会受到刺激。皮质醇调节几种基因的转录,主要通过激活糖皮质激素受体(GR)。先前,我们在体内和体外的药理学/糖皮质激素挑战后显示出 PERIOD 基因 PER1 和 PER3 的上调。本研究旨在研究未受刺激的、昼夜皮质醇分泌与选定的 GR 靶基因(PER1、PER2、PER3、FKBP5、GILZ 和 SDPR)在体内表达之间的时间关联,以确定皮质醇和 mRNA 表达之间最显著耦合的时间。在 18 名健康男性中,从清晨到 16:00 点,每 15 分钟测量一次未受刺激的血浆和唾液皮质醇浓度以及全血中的基因表达水平。评估皮质醇浓度与 mRNA 表达水平的时间滞后相关性,允许滞后时间在-240 到+240 分钟之间。在非零滞后时间,皮质醇水平与 FKBP5(血浆:r=0.74(CI=0.65-0.81),p<0.001,滞后+90 分钟;唾液:r=0.71(CI=0.61-0.78),p<0.001,滞后+75 分钟)和 GILZ(血浆:r=0.59(CI=0.46-0.69),p<0.001,滞后+30 分钟;唾液 r=0.53(CI=0.41-0.63),p<0.001,滞后+15 分钟)的表达之间观察到强烈的正相关。PERIOD 基因和 SDPR 的表达与皮质醇仅微弱相关(所有 |r| <0.25)。我们的发现表明,在未受刺激的条件下,人类的皮质醇分泌与基因表达之间存在强烈的相关性。观察到的时间滞后可以指导未来的研究,旨在对具有应激相关障碍的临床样本中的糖皮质激素依赖性基因表达进行特征描述。