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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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 |
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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 |
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