睡眠剥夺会损害空间记忆,并降低海马体中细胞外信号调节激酶的磷酸化水平。

Sleep deprivation impairs spatial memory and decreases extracellular signal-regulated kinase phosphorylation in the hippocampus.

作者信息

Guan Zhiwei, Peng Xuwen, Fang Jidong

机构信息

Department of Psychiatry, Pennsylvania State University College of Medicine, Hershey 17033, USA.

出版信息

Brain Res. 2004 Aug 20;1018(1):38-47. doi: 10.1016/j.brainres.2004.05.032.

Abstract

Loss of sleep may result in memory impairment. However, little is known about the biochemical basis for memory deficits induced by sleep deprivation. Extracellular signal-regulated kinase (ERK) is involved in memory consolidation in different tasks. Phosphorylation of ERK is necessary for its activation and is an important step in mediating neuronal responses to synaptic activities. The aim of the present study was to determine the effects of total sleep deprivation (TSD) on memory and ERK phosphorylation in the brain. Rats were trained in Morris water maze to find a hidden platform (a spatial task) or a visible platform (a nonspatial task) after 6 h TSD or spontaneous sleep. TSD had no effect on spatial learning, but significantly impaired spatial memory tested 24 h after training. Nonspatial learning and memory were not impaired by TSD. Phospho-ERK levels in the hippocampus were significantly reduced after 6 h TSD compared to the controls and returned to the control levels after 2 h recovery sleep. Total ERK1 and ERK2 were slightly increased after 6 h TSD and returned to the control levels after 2 h recovery sleep. These alterations were not observed in the cortex after TSD. Protein phosphotase-1 and mitogen-activated protein kinase phosphatase-2, which dephosphorylates phospho-ERK, were also measured, but they were not altered by TSD. The impairments of both spatial memory and ERK phosphorylation indicate that the hippocampus is vulnerable to sleep loss. These results are consistent with the idea that decreased ERK activation in the hippocampus is involved in sleep deprivation-induced spatial memory impairment.

摘要

睡眠缺失可能导致记忆障碍。然而,关于睡眠剥夺引起记忆缺陷的生化基础却知之甚少。细胞外信号调节激酶(ERK)参与不同任务中的记忆巩固。ERK的磷酸化是其激活所必需的,并且是介导神经元对突触活动反应的重要步骤。本研究的目的是确定完全睡眠剥夺(TSD)对大脑记忆和ERK磷酸化的影响。将大鼠在6小时TSD或自然睡眠后,在莫里斯水迷宫中训练以寻找隐藏平台(空间任务)或可见平台(非空间任务)。TSD对空间学习没有影响,但在训练后24小时测试时显著损害空间记忆。TSD并未损害非空间学习和记忆。与对照组相比,6小时TSD后海马体中的磷酸化ERK水平显著降低,在2小时恢复睡眠后恢复到对照水平。6小时TSD后总ERK1和ERK2略有增加,在2小时恢复睡眠后恢复到对照水平。TSD后在皮质中未观察到这些变化。还测量了使磷酸化ERK去磷酸化的蛋白磷酸酶-1和丝裂原活化蛋白激酶磷酸酶-2,但它们未因TSD而改变。空间记忆和ERK磷酸化的损害表明海马体易受睡眠缺失的影响。这些结果与海马体中ERK激活降低参与睡眠剥夺诱导的空间记忆损害这一观点一致。

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