Chennaoui Mounir, Arnal Pierrick J, Drogou Catherine, Leger Damien, Sauvet Fabien, Gomez-Merino Danielle
Fatigue and Vigilance team, Neuroscience and Operational Constraints Department, French Armed Forces Biomedical Research Institute (IRBA)Brétigny-sur-Orge, France.
VIFASOM team (EA 7330), Paris Desacrtes University, Sorbonne Paris CitéHôtel Dieu, Paris, France.
Front Neurosci. 2017 May 2;11:240. doi: 10.3389/fnins.2017.00240. eCollection 2017.
The purinergic type P1 (adenosine A and A) receptors and the type P2 (X7) receptor have been suggested to mediate physiological effects of adenosine and adenosine triphosphate on sleep. We aimed to determine gene expression of AR (receptor), AR, and P2RX in leukocytes of healthy subjects during total sleep deprivation followed by sleep recovery. Expression of the pro-inflammatory cytokines IL-1β and TNF-α were also determined as they have been characterized as sleep regulatory substances, via P2RX activation. Blood sampling was performed on 14 young men (aged 31.9 ± 3.9) at baseline (B), after 24 h of sleep deprivation (24 h-), and after one night of sleep recovery (R). We compared gene expression levels after six nights of habitual (22.30-07.00) or extended (21.00-07.00) bedtimes. Using quantitative real-time PCR, the amount of mRNA for AR, AR, P2RX, TNF-α, and IL-1β was analyzed. After 24 h- compared to B, whatever prior sleep condition, a significant increase of AR expression was observed that returned to basal level after sleep recovery [day main effect, = 10.8, < 0.001]. In both sleep condition, a day main effect on P2RX mRNA was observed [ = 6.7, = 0.005] with significant increases after R compared with 24 h-. TNF-α and IL-1β expressions were not significantly altered. Before 24 h- (baseline), the AR expression was negatively correlated with the latency of stage 3 sleep during the previous night, while that of the AR positively. This was not observed after sleep recovery following 24 h-. This is the first study showing increased AR and not A gene expression after 24 h- in leukocytes of healthy subjects, and this even if bedtime was initially increased by 1.5 h per night for six nights. In conclusion, prolonged wakefulness induced an up-regulation of the A2A receptor gene expression in leukocytes from healthy subjects. Significant correlations between baseline expression of A and A receptors in peripheral cells and stage 3 sleep suggested their involvement in mediating the effects of adenosine on sleep.
嘌呤能P1型(腺苷A1和A2A)受体及P2型(P2X7)受体被认为介导腺苷和三磷酸腺苷对睡眠的生理作用。我们旨在确定完全睡眠剥夺后再恢复睡眠期间,健康受试者白细胞中A1R(受体)、A2AR及P2RX7的基因表达情况。还测定了促炎细胞因子IL-1β和TNF-α的表达,因为它们已被确定为通过P2RX7激活的睡眠调节物质。对14名年轻男性(年龄31.9±3.9岁)在基线期(B)、睡眠剥夺24小时后(24h-)及一晚睡眠恢复后(R)进行采血。我们比较了习惯性(22:30 - 07:00)或延长(21:00 - 07:00)就寝时间6晚后的基因表达水平。采用定量实时PCR分析A1R、A2AR、P2RX7、TNF-α及IL-1β的mRNA量。与B相比,无论之前的睡眠状况如何,24h-后A2AR表达均显著增加,睡眠恢复后恢复至基础水平[日主效应,F = 10.8,P < 0.001]。在两种睡眠状况下,均观察到日主效应作用于P2RX7 mRNA[F = 6.7,P = 0.005],R期与24h-相比显著增加。TNF-α和IL-1β表达无显著改变。在24h-(基线)之前,A1R表达与前一晚3期睡眠潜伏期呈负相关,而A2AR呈正相关。24h-睡眠恢复后未观察到此现象。这是第一项显示健康受试者白细胞在24h-后A2AR而非A1R基因表达增加的研究,即使就寝时间最初连续6晚每晚增加1.5小时也是如此。总之,长时间觉醒诱导健康受试者白细胞中A2A受体基因表达上调。外周细胞中A1和A2A受体的基线表达与3期睡眠之间的显著相关性表明它们参与介导腺苷对睡眠的作用。