首页> 外文期刊>Behavioural Brain Research: An International Journal >Short-term sleep deprivation impairs spatial working memory and modulates expression levels of ionotropic glutamate receptor subunits in hippocampus
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Short-term sleep deprivation impairs spatial working memory and modulates expression levels of ionotropic glutamate receptor subunits in hippocampus

机译:短期睡眠剥夺损害空间工作记忆并调节海马离子型谷氨酸受体亚基的表达水平

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Hippocampus-dependent learning memory is sensitive to sleep deprivation (SD). Although the ionotropic glutamate receptors play a vital role in synaptic plasticity and learning and memory, however, whether the expression of these receptor subunits is modulated by sleep loss remains unclear. In the present study, western blotting was performed by probing with specific antibodies against the ionotropic cxamino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunits GluA1, GluA2, GluA3, and against the N-methyl-o-aspartate (NMDA) glutamate receptor subunits GluN1, GluN2A, GluN2B. In hippocampus, down regulation of surface GluA1 and GluN2A surface expression were observed in both SD groups. However, surface expression level of GluA2, GluA3, GluN1 and GluN2B was significantly upregulated in 8 h-SD rats when compared to the 4 h-SD rats. In parallel with the complex changes in AMPA and NMDA receptor subunit expressions, we found the 8 h-SD impaired rat spatial working memory in 30-s-delay T-maze task, whereas no impairment of spatial learning was observed in 4 h-SD rats. These results indicate that sleep loss alters the relative expression levels of the AMPA and NMDA receptors, thus affects the synaptic strength and capacity for plasticity and partially contributes to spatial memory impairment. (C) 2015 Published by Elsevier B.V.
机译:海马依赖性学习记忆对睡眠剥夺(SD)敏感。尽管离子型谷氨酸受体在突触可塑性和学习记忆中起着至关重要的作用,但是,这些受体亚基的表达是否受睡眠丧失的调节尚不清楚。在本研究中,蛋白质印迹是通过针对抗离子型cxamino-3-hydroxy-5-methyl-4-isoxazole丙酸(AMPA)受体亚基GluA1,GluA2,GluA3和N-甲基-o的特异性抗体进行探测的-天冬氨酸(NMDA)谷氨酸受体亚基GluN1,GluN2A,GluN2B。在海马中,在两个SD组中均观察到表面GluA1和GluN2A表面表达的下调。然而,与4h-SD大鼠相比,在8h-SD大鼠中GluA2,GluA3,GluN1和GluN2B的表面表达水平显着上调。与AMPA和NMDA受体亚基表达的复杂变化并行,我们发现30 h延迟T迷宫任务中8 h-SD受损的大鼠空间工作记忆,而在4 h-SD中未观察到空间学习障碍大鼠。这些结果表明,睡眠不足会改变AMPA和NMDA受体的相对表达水平,从而影响突触强度和可塑性,部分导致空间记忆受损。 (C)2015由Elsevier B.V.发布

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