Cargando…

Differential modulation of NREM sleep regulation and EEG topography by chronic sleep restriction in mice

Compensatory elevation in NREM sleep EEG delta power has been typically observed following prolonged wakefulness and widely used as a sleep homeostasis indicator. However, recent evidence in human and rodent chronic sleep restriction (CSR) studies suggests that NREM delta power is not progressively...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Bowon, Hwang, Eunjin, Strecker, Robert E., Choi, Jee Hyun, Kim, Youngsoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954245/
https://www.ncbi.nlm.nih.gov/pubmed/31924847
http://dx.doi.org/10.1038/s41598-019-54790-y
_version_ 1783486771478134784
author Kim, Bowon
Hwang, Eunjin
Strecker, Robert E.
Choi, Jee Hyun
Kim, Youngsoo
author_facet Kim, Bowon
Hwang, Eunjin
Strecker, Robert E.
Choi, Jee Hyun
Kim, Youngsoo
author_sort Kim, Bowon
collection PubMed
description Compensatory elevation in NREM sleep EEG delta power has been typically observed following prolonged wakefulness and widely used as a sleep homeostasis indicator. However, recent evidence in human and rodent chronic sleep restriction (CSR) studies suggests that NREM delta power is not progressively increased despite of accumulated sleep loss over days. In addition, there has been little progress in understanding how sleep EEG in different brain regions responds to CSR. Using novel high-density EEG electrode arrays in the mouse model of CSR where mice underwent 18-h sleep deprivation per day for 5 consecutive days, we performed an extensive analysis of topographical NREM sleep EEG responses to the CSR condition, including period-amplitude analysis of individual slow waves. As previously reported in our analysis of REM sleep responses, we found different patterns of changes: (i) progressive decrease in NREM sleep duration and consolidation, (ii) persistent enhancement in NREM delta power especially in the frontal and parietal regions, and (iii) progressive increases in individual slow wave slope and frontal fast oscillation power. These results suggest that multiple sleep-wake regulatory systems exist in a brain region-specific manner, which can be modulated independently, especially in the CSR condition.
format Online
Article
Text
id pubmed-6954245
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-69542452020-01-15 Differential modulation of NREM sleep regulation and EEG topography by chronic sleep restriction in mice Kim, Bowon Hwang, Eunjin Strecker, Robert E. Choi, Jee Hyun Kim, Youngsoo Sci Rep Article Compensatory elevation in NREM sleep EEG delta power has been typically observed following prolonged wakefulness and widely used as a sleep homeostasis indicator. However, recent evidence in human and rodent chronic sleep restriction (CSR) studies suggests that NREM delta power is not progressively increased despite of accumulated sleep loss over days. In addition, there has been little progress in understanding how sleep EEG in different brain regions responds to CSR. Using novel high-density EEG electrode arrays in the mouse model of CSR where mice underwent 18-h sleep deprivation per day for 5 consecutive days, we performed an extensive analysis of topographical NREM sleep EEG responses to the CSR condition, including period-amplitude analysis of individual slow waves. As previously reported in our analysis of REM sleep responses, we found different patterns of changes: (i) progressive decrease in NREM sleep duration and consolidation, (ii) persistent enhancement in NREM delta power especially in the frontal and parietal regions, and (iii) progressive increases in individual slow wave slope and frontal fast oscillation power. These results suggest that multiple sleep-wake regulatory systems exist in a brain region-specific manner, which can be modulated independently, especially in the CSR condition. Nature Publishing Group UK 2020-01-10 /pmc/articles/PMC6954245/ /pubmed/31924847 http://dx.doi.org/10.1038/s41598-019-54790-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Bowon
Hwang, Eunjin
Strecker, Robert E.
Choi, Jee Hyun
Kim, Youngsoo
Differential modulation of NREM sleep regulation and EEG topography by chronic sleep restriction in mice
title Differential modulation of NREM sleep regulation and EEG topography by chronic sleep restriction in mice
title_full Differential modulation of NREM sleep regulation and EEG topography by chronic sleep restriction in mice
title_fullStr Differential modulation of NREM sleep regulation and EEG topography by chronic sleep restriction in mice
title_full_unstemmed Differential modulation of NREM sleep regulation and EEG topography by chronic sleep restriction in mice
title_short Differential modulation of NREM sleep regulation and EEG topography by chronic sleep restriction in mice
title_sort differential modulation of nrem sleep regulation and eeg topography by chronic sleep restriction in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954245/
https://www.ncbi.nlm.nih.gov/pubmed/31924847
http://dx.doi.org/10.1038/s41598-019-54790-y
work_keys_str_mv AT kimbowon differentialmodulationofnremsleepregulationandeegtopographybychronicsleeprestrictioninmice
AT hwangeunjin differentialmodulationofnremsleepregulationandeegtopographybychronicsleeprestrictioninmice
AT streckerroberte differentialmodulationofnremsleepregulationandeegtopographybychronicsleeprestrictioninmice
AT choijeehyun differentialmodulationofnremsleepregulationandeegtopographybychronicsleeprestrictioninmice
AT kimyoungsoo differentialmodulationofnremsleepregulationandeegtopographybychronicsleeprestrictioninmice