Literature DB >> 25325451

Characterization of topographically specific sleep spindles in mice.

Dongwook Kim1, Eunjin Hwang2, Mina Lee3, Hokun Sung4, Jee Hyun Choi1.   

Abstract

STUDY
OBJECTIVE: Sleep spindles in humans have been classified as slow anterior and fast posterior spindles; recent findings indicate that their profiles differ according to pharmacology, pathology, and function. However, little is known about the generation mechanisms within the thalamocortical system for different types of spindles. In this study, we aim to investigate the electrophysiological behaviors of the topographically distinctive spindles within the thalamocortical system by applying high-density EEG and simultaneous thalamic LFP recordings in mice.
DESIGN: 32-channel extracranial EEG and 2-channel thalamic LFP were recorded simultaneously in freely behaving mice to acquire spindles during spontaneous sleep.
SUBJECTS: Hybrid F1 male mice of C57BL/6J and 129S4/svJae. MEASUREMENTS AND
RESULTS: Spindle events in each channel were detected by spindle detection algorithm, and then a cluster analysis was applied to classify the topographically distinctive spindles. All sleep spindles were successfully classified into 3 groups: anterior, posterior, and global spindles. Each spindle type showed distinct thalamocortical activity patterns regarding the extent of similarity, phase synchrony, and time lags between cortical and thalamic areas during spindle oscillation. We also found that sleep slow waves were likely to associate with all types of sleep spindles, but also that the ongoing cortical decruitment/ recruitment dynamics before the onset of spindles and their relationship with spindle generation were also variable, depending on the spindle types.
CONCLUSION: Topographically specific sleep spindles show distinctive thalamocortical network behaviors.
© 2014 Associated Professional Sleep Societies, LLC.

Entities:  

Keywords:  high-density EEG; mouse; sleep slow waves; sleep spindles; thalamic LFP; thalamocortical networks; topography

Mesh:

Year:  2015        PMID: 25325451      PMCID: PMC4262960          DOI: 10.5665/sleep.4330

Source DB:  PubMed          Journal:  Sleep        ISSN: 0161-8105            Impact factor:   5.849


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