Ravassard Pascal, Hamieh Al Mahdy, Joseph Mickaël Antoine, Fraize Nicolas, Libourel Paul-Antoine, Lebarillier Léa, Arthaud Sébastien, Meissirel Claire, Touret Monique, Malleret Gaël, Salin Paul-Antoine
Centre National de la Recherche Scientifique (CNRS), Unité Mixte de Recherche 5292 ; Institut National de la Santé et de la Recherche Médicale (INSERM), Unité 1028, Lyon Cedex 08, France.
Physiopathology of the Sleep Neuronal Networks, Lyon Neuroscience Research Center, F-69008 Lyon, France.
Cereb Cortex. 2016 Apr;26(4):1488-1500. doi: 10.1093/cercor/bhu310. Epub 2015 Jan 13.
Prolonged rapid-eye-movement (REM) sleep deprivation has long been used to study the role of REM sleep in learning and memory processes. However, this method potentially induces stress and fatigue that may directly affect cognitive functions. Here, by using a short-term and nonstressful REM sleep deprivation (RSD) method we assessed in rats the bidirectional influence of reduced and increased REM sleep amount on hippocampal-dependent emotional memory and plasticity. Our results indicate that 4 h RSD impaired consolidation of contextual fear conditioning (CFC) and induction of long-term potentiation (LTP), while decreasing density of Egr1/Zif268-expressing neurons in the CA1 region of the dorsal hippocampus. LTP and Egr1 expression were not affected in ventral CA1. Conversely, an increase in REM sleep restores and further facilitates CFC consolidation and LTP induction, and also increases Egr1 expression in dorsal CA1. Moreover, CFC consolidation, Egr1 neuron density, and LTP amplitude in dorsal CA1 show a positive correlation with REM sleep amount. Altogether, these results indicate that mild changes in REM sleep amount bidirectionally affect memory and synaptic plasticity mechanisms occurring in the CA1 area of the dorsal hippocampus.
长期快速眼动(REM)睡眠剥夺一直被用于研究REM睡眠在学习和记忆过程中的作用。然而,这种方法可能会诱发压力和疲劳,进而可能直接影响认知功能。在此,我们通过使用一种短期且无压力的REM睡眠剥夺(RSD)方法,在大鼠中评估了REM睡眠量减少和增加对海马体依赖性情绪记忆及可塑性的双向影响。我们的结果表明,4小时的RSD损害了情境恐惧条件反射(CFC)的巩固以及长时程增强(LTP)的诱导,同时降低了背侧海马体CA1区中表达Egr1/Zif268的神经元密度。腹侧CA1区的LTP和Egr1表达未受影响。相反,REM睡眠增加可恢复并进一步促进CFC巩固和LTP诱导,还可增加背侧CA1区的Egr1表达。此外,背侧CA1区的CFC巩固、Egr1神经元密度和LTP幅度与REM睡眠量呈正相关。总之,这些结果表明REM睡眠量的轻微变化对背侧海马体CA1区发生的记忆和突触可塑性机制具有双向影响。