Sleep is necessary for experience-dependent sequence plasticity in mouse primary visual cortex

被引:0
|
作者
Hosamane, Nishitha S. [1 ]
Didouchevski, Adam M. [1 ,2 ]
Malci, Ayse [1 ]
Gavornik, Jeffrey P. [3 ]
Sidorov, Michael S. [1 ,4 ,5 ]
机构
[1] Childrens Natl Med Ctr, Ctr Neurosci Res, Washington, DC 20010 USA
[2] Univ Maryland, College Pk, MD USA
[3] Boston Univ, Dept Biol, Boston, MA USA
[4] George Washington Univ, Sch Med & Hlth Sci, Dept Pediat, Washington, DC 20052 USA
[5] George Washington Univ, Sch Med & Hlth Sci, Dept Pharmacol & Physiol, Washington, DC 20052 USA
关键词
experience-dependent plasticity; primary visual cortex; in vivo electrophysiology; sleep; MEMORY; CONSOLIDATION; RECOGNITION; HIPPOCAMPUS; REPLAY; EEG;
D O I
10.1093/sleep/zsae262
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study objectives: Repeated exposure to familiar visual sequences drives experience-dependent and sequence-specific plasticity in mouse primary visual cortex (V1). Prior work demonstrated a critical role for sleep in consolidating a related but mechanistically distinct form of experience-dependent plasticity in V1. Here, we assessed the role of sleep in consolidation of spatiotemporal sequence learning (sequence plasticity) in mouse V1. Methods: Visually evoked potentials (VEPs) were recorded in awake, head-fixed mice viewing sequences of four visual stimuli. Each sequence was presented 200 times per session, across multiple sessions, to drive plasticity. The effects of sleep consolidation time and sleep deprivation on plasticity were assessed. Results: Sequence plasticity occurred in V1 following as little as one hour of ad libitum sleep and increased with longer periods of sleep. Sleep deprivation blocked sequence plasticity consolidation, which recovered following subsequent sleep. Conclusions: Sleep is required for the consolidation of sequence plasticity in mouse V1.
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页数:9
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