Team "SLEEP", Centre de Recherche en Neurosciences de Lyon (CRNL), UMR 5292 CNRS/U1028 INSERM and Université de Lyon, Lyon I, Neurocampus, 95 Boulevard Pinel, 69500 Bron, France; Brain Institute, Federal University of Rio Grande do Norte, Natal, RN, Brazil.
Team "SLEEP", Centre de Recherche en Neurosciences de Lyon (CRNL), UMR 5292 CNRS/U1028 INSERM and Université de Lyon, Lyon I, Neurocampus, 95 Boulevard Pinel, 69500 Bron, France.
Biochem Pharmacol. 2021 Sep;191:114514. doi: 10.1016/j.bcp.2021.114514. Epub 2021 Mar 11.
Michel Jouvet proposed in 1959 that REM sleep is a paradoxical state since it was characterized by the association of a cortical activation similar to wakefulness (W) with muscle atonia. Recently, we showed using cFos as a marker of activity that cortical activation during paradoxical sleep (PS) was limited to a few limbic cortical structures in contrast to W during which all cortices were strongly activated. However, we were not able to demonstrate whether the same neurons are activated during PS and W and to rule out that the activation observed was not linked with stress induced by the flowerpot method of PS deprivation. In the present study, we answered to these two questions by combining tdTomato and cFos immunostaining in the innovative TRAP2 transgenic mice exposed one week apart to two periods of W (W-W mice), PS rebound (PSR-PSR) or a period of W followed by a period of PSR (W-PSR mice). Using such method, we showed that different neurons are activated during W and PSR in the anterior cingulate (ACA) and rostral and caudal retrosplenial (rRSP and cRSP) cortices as well as the claustrum (CLA) previously shown to contain a large number of activated neurons after PSR. Further, the distribution of the neurons during PSR in the rRSP and cRSP was limited to the superficial layers while it was widespread across all layers during W. Our results clearly show at the cellular level that PS and W are two completely different states in term of neocortical activation.
米歇尔·朱维特(Michel Jouvet)于 1959 年提出,快速眼动(REM)睡眠是一种矛盾状态,因为它的特征是皮质兴奋类似于觉醒(W)与肌肉弛缓同时存在。最近,我们使用 cFos 作为活动标志物表明,在 REM 睡眠(PS)期间的皮质激活仅限于几个边缘皮质结构,而在 W 期间,所有皮质都被强烈激活。然而,我们无法证明在 PS 和 W 期间是否激活了相同的神经元,也无法排除观察到的激活与 PS 剥夺的花盆方法引起的应激无关。在本研究中,我们通过在创新的 TRAP2 转基因小鼠中结合 tdTomato 和 cFos 免疫染色,分别在一周内暴露于 W(W-W 小鼠)、PS 反弹(PSR-PSR)或 W 后 PSR 期(W-PSR 小鼠),回答了这两个问题。使用这种方法,我们表明在 ACA 以及额侧和尾侧后扣带回(rRSP 和 cRSP)皮质和屏状核(CLA)中,不同的神经元在 W 和 PSR 期间被激活,这些区域在 PSR 后都含有大量激活的神经元。此外,在 rRSP 和 cRSP 中,PSR 期间神经元的分布仅限于浅层,而在 W 期间则广泛分布于所有层。我们的研究结果清楚地表明,在细胞水平上,PS 和 W 在新皮质激活方面是两种完全不同的状态。