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Differential effect of sleep deprivation on place cell representations, sleep architecture, and memory in young and old mice

机译:睡眠剥夺对年轻和老年小鼠的睡眠剥夺睡眠剥夺的差异效果

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Poor sleep quality is associated with age-related cognitive decline, and whether reversal of these alterations is possible is unknown. In this study, we report how sleep deprivation (SD) affects hippocampal representations, sleep patterns, and memory in young and old mice. After training in a hippocampus-dependent object-place recognition (OPR) task, control animals sleep ad libitum , although experimental animals undergo 5?h of SD, followed by recovery sleep. Young controls and old SD mice exhibit successful OPR memory, whereas young SD and old control mice are impaired. Successful performance is associated with two cellular phenotypes: (1) “context” cells, which remain stable throughout training and testing, and (2) “object configuration” cells, which remap when objects are introduced to the context and during testing. Additionally, effective memory correlates with spindle counts during non-rapid eye movement (NREM)/rapid eye movement (REM) sigma transitions. These results suggest SD may serve to ameliorate age-related memory deficits and allow hippocampal representations to adapt to changing environments.
机译:睡眠质量差与年龄相关的认知下降相关,以及这些改变的逆转是否有可能是未知的。在这项研究中,我们报告了睡眠剥夺(SD)如何影响年轻和旧小鼠中的海马表示,睡眠模式和记忆。在培训海马依赖的对象识别(OPR)任务后,控制动物睡眠睡眠,尽管实验动物经历了5?H的SD,其次是恢复睡眠。年轻的控制和旧的SD老鼠表现出成功的OPR记忆,而年轻的SD和旧对照小鼠受损。成功的性能与两个蜂窝成像型相关联:(1)“上下文”细胞,其在整个训练和测试过程中保持稳定,并且(2)“对象配置”单元格,当对象被引入上下文和测试期间,该细胞重新映射。另外,有效的存储器在非快速眼运动期间与主轴计数相关(NREM)/快速眼运动(REM)Sigma转换。这些结果表明SD可以用于改善与年龄相关的记忆缺陷,并允许海马表示适应改变环境。

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