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dc.contributor.authorKim, Bowon-
dc.contributor.authorKocsis, Bernat-
dc.contributor.authorHwang, Eunjin-
dc.contributor.authorKim, Youngsoo-
dc.contributor.authorStrecker, Robert E.-
dc.contributor.authorMcCarley, Robert W.-
dc.contributor.authorChoi, Jee Hyun-
dc.date.accessioned2024-01-20T02:30:31Z-
dc.date.available2024-01-20T02:30:31Z-
dc.date.created2021-09-01-
dc.date.issued2017-02-
dc.identifier.issn0027-8424-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/123147-
dc.description.abstractHomeostatic rebound in rapid eye movement (REM) sleep normally occurs after acute sleep deprivation, but REM sleep rebound settles on a persistently elevated level despite continued accumulation of REM sleep debt during chronic sleep restriction (CSR). Using highdensity EEG in mice, we studied how this pattern of global regulation is implemented in cortical regions with different functions and network architectures. We found that across all areas, slow oscillations repeated the behavioral pattern of persistent enhancement during CSR, whereas high-frequency oscillations showed progressive increases. This pattern followed a common rule despite marked topographic differences. The findings suggest that REM sleep slow oscillations may translate top-down homeostatic control to widely separated brain regions whereas fast oscillations synchronizing local neuronal ensembles escape this global command. These patterns of EEG oscillation changes are interpreted to reconcile two prevailing theories of the function of sleep, synaptic homeostasis and sleep dependent memory consolidation.-
dc.languageEnglish-
dc.publisherNational Academy of Sciences-
dc.titleDifferential modulation of global and local neural oscillations in REM sleep by homeostatic sleep regulation-
dc.typeArticle-
dc.identifier.doi10.1073/pnas.1615230114-
dc.description.journalClass1-
dc.identifier.bibliographicCitationProceedings of the National Academy of Sciences of the United States of America, v.114, no.9, pp.E1727 - E1736-
dc.citation.titleProceedings of the National Academy of Sciences of the United States of America-
dc.citation.volume114-
dc.citation.number9-
dc.citation.startPageE1727-
dc.citation.endPageE1736-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000395101200019-
dc.identifier.scopusid2-s2.0-85014122568-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.type.docTypeArticle-
dc.subject.keywordPlusPONTINE-WAVE GENERATOR-
dc.subject.keywordPlusEYE-MOVEMENT SLEEP-
dc.subject.keywordPlusGAMMA-OSCILLATIONS-
dc.subject.keywordPlusCORTICAL NETWORK-
dc.subject.keywordPlusVIGILANCE STATE-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusHZ OSCILLATION-
dc.subject.keywordPlusSPATIAL MEMORY-
dc.subject.keywordPlusBRAIN RHYTHMS-
dc.subject.keywordPlusTHETA RHYTHM-
dc.subject.keywordAuthorchronic sleep deprivation-
dc.subject.keywordAuthorlow-frequency cortical oscillation-
dc.subject.keywordAuthorfast corticaloscillation-
dc.subject.keywordAuthorEEG topography-
dc.subject.keywordAuthorsleep function-
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