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睡眠剥夺会损害恢复睡眠期间学习诱导的海马体尖波涟漪增加及相关的放电活动。

Sleep Deprivation Impairs Learning-Induced Increase in Hippocampal Sharp Wave Ripples and Associated Spike Dynamics during Recovery Sleep.

作者信息

Li Rong-Rong, Yan Jie, Chen Hao, Zhang Wei-Wei, Hu Yu-Bo, Zhang Jie, Hu Zhi-An, Xiong Yan, Yao Zhong-Xiang, Hu Bo

机构信息

Department of Physiology, College of Basic Medical Sciences, Army Medical University, Chongqing 400038, China.

Experimental Center of Basic Medicine, College of Basic Medical Sciences, Army Medical University, Chongqing 400038, China.

出版信息

Cereb Cortex. 2022 Feb 8;32(4):824-838. doi: 10.1093/cercor/bhab247.

Abstract

Sleep deprivation (SD) causes deficits in off-line memory consolidation, but the underlying network oscillation mechanisms remain unclear. Hippocampal sharp wave ripple (SWR) oscillations play a critical role in off-line memory consolidation. Therefore, we trained mice to learn a hippocampus-dependent trace eyeblink conditioning (tEBC) task and explored the influence of 1.5-h postlearning SD on hippocampal SWRs and related spike dynamics during recovery sleep. We found an increase in hippocampal SWRs during postlearning sleep, which predicted the consolidation of tEBC in conditioned mice. In contrast, sleep-deprived mice showed a loss of tEBC learning-induced increase in hippocampal SWRs during recovery sleep. Moreover, the sleep-deprived mice exhibited weaker reactivation of tEBC learning-associated pyramidal cells in hippocampal SWRs during recovery sleep. In line with these findings, tEBC consolidation was impaired in sleep-deprived mice. Furthermore, sleep-deprived mice showed augmented fast excitation from pyramidal cells to interneurons and enhanced participation of interneurons in hippocampal SWRs during recovery sleep. Among various interneurons, parvalbumin-expressing interneurons specifically exhibited overexcitation during hippocampal SWRs. Our findings suggest that altered hippocampal SWRs and associated spike dynamics during recovery sleep may be candidate network oscillation mechanisms underlying SD-induced memory deficits.

摘要

睡眠剥夺(SD)会导致离线记忆巩固出现缺陷,但其潜在的网络振荡机制仍不清楚。海马体尖波涟漪(SWR)振荡在离线记忆巩固中起关键作用。因此,我们训练小鼠学习一项依赖海马体的痕迹眨眼条件反射(tEBC)任务,并探究学习后1.5小时的睡眠剥夺对恢复睡眠期间海马体SWR以及相关尖峰动力学的影响。我们发现学习后睡眠期间海马体SWR增加,这预测了条件反射小鼠中tEBC的巩固。相比之下,睡眠剥夺的小鼠在恢复睡眠期间tEBC学习诱导的海马体SWR增加消失。此外,睡眠剥夺的小鼠在恢复睡眠期间海马体SWR中与tEBC学习相关的锥体细胞的再激活较弱。与这些发现一致,睡眠剥夺的小鼠中tEBC巩固受损。此外,睡眠剥夺的小鼠在恢复睡眠期间显示出从锥体细胞到中间神经元的快速兴奋增强,以及中间神经元在海马体SWR中的参与增加。在各种中间神经元中,表达小白蛋白的中间神经元在海马体SWR期间特别表现出过度兴奋。我们的发现表明,恢复睡眠期间海马体SWR和相关尖峰动力学的改变可能是睡眠剥夺诱导的记忆缺陷潜在的网络振荡机制候选因素。

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