Freyburger Marlène, Poirier Gaétan, Carrier Julie, Mongrain Valérie
Center for Advanced Research in Sleep Medicine and Research Center, Hôpital du Sacré-Coeur de Montréal, Montreal, QC, Canada.
Department of Neuroscience, Université de Montréal, Montreal, QC, Canada.
J Sleep Res. 2017 Oct;26(5):539-546. doi: 10.1111/jsr.12532. Epub 2017 May 10.
Slow waves occurring during non-rapid eye movement sleep have been associated with neurobehavioural performance and memory. In addition, the duration of previous wakefulness and sleep impacts characteristics of these slow waves. However, molecular mechanisms regulating the dynamics of slow-wave characteristics remain poorly understood. The EphA4 receptor regulates glutamatergic transmission and synaptic plasticity, which have both been linked to sleep slow waves. To investigate if EphA4 regulates slow-wave characteristics during non-rapid eye movement sleep, we compared individual parameters of slow waves between EphA4 knockout mice and wild-type littermates under baseline conditions and after a 6-h sleep deprivation. We observed that, compared with wild-type mice, knockout mice display a shorter duration of positive and negative phases of slow waves under baseline conditions and after sleep deprivation. However, the mutation did not change slow-wave density, amplitude and slope, and did not affect the sleep deprivation-dependent changes in slow-wave characteristics, suggesting that EphA4 is not involved in the response to elevated sleep pressure. Our present findings suggest a role for EphA4 in shaping cortical oscillations during sleep that is independent from sleep need.
非快速眼动睡眠期间出现的慢波与神经行为表现和记忆有关。此外,先前清醒和睡眠的时长会影响这些慢波的特征。然而,调节慢波特征动态变化的分子机制仍知之甚少。EphA4受体调节谷氨酸能传递和突触可塑性,这两者都与睡眠慢波有关。为了研究EphA4是否在非快速眼动睡眠期间调节慢波特征,我们比较了EphA4基因敲除小鼠和野生型同窝小鼠在基线条件下以及6小时睡眠剥夺后的慢波个体参数。我们观察到,与野生型小鼠相比,基因敲除小鼠在基线条件下和睡眠剥夺后慢波正负相的持续时间较短。然而,该突变并未改变慢波密度、振幅和斜率,也未影响睡眠剥夺引起的慢波特征变化,这表明EphA4不参与对升高的睡眠压力的反应。我们目前的研究结果表明,EphA4在塑造睡眠期间的皮质振荡中发挥作用,且该作用独立于睡眠需求。