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Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep
Sleep-wake driven changes in non-rapid-eye-movement sleep (NREM) sleep (NREMS) EEG delta (δ-)power are widely used as proxy for a sleep homeostatic process. Here, we noted frequency increases in δ-waves in sleep-deprived mice, prompting us to re-evaluate how slow-wave characteristics relate to prior...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7305232/ https://www.ncbi.nlm.nih.gov/pubmed/32561733 http://dx.doi.org/10.1038/s41467-020-16915-0 |
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author | Hubbard, Jeffrey Gent, Thomas C. Hoekstra, Marieke M. B. Emmenegger, Yann Mongrain, Valerie Landolt, Hans-Peter Adamantidis, Antoine R. Franken, Paul |
author_facet | Hubbard, Jeffrey Gent, Thomas C. Hoekstra, Marieke M. B. Emmenegger, Yann Mongrain, Valerie Landolt, Hans-Peter Adamantidis, Antoine R. Franken, Paul |
author_sort | Hubbard, Jeffrey |
collection | PubMed |
description | Sleep-wake driven changes in non-rapid-eye-movement sleep (NREM) sleep (NREMS) EEG delta (δ-)power are widely used as proxy for a sleep homeostatic process. Here, we noted frequency increases in δ-waves in sleep-deprived mice, prompting us to re-evaluate how slow-wave characteristics relate to prior sleep-wake history. We identified two classes of δ-waves; one responding to sleep deprivation with high initial power and fast, discontinuous decay during recovery sleep (δ2) and another unrelated to time-spent-awake with slow, linear decay (δ1). Reanalysis of previously published datasets demonstrates that δ-band heterogeneity after sleep deprivation is also present in human subjects. Similar to sleep deprivation, silencing of centromedial thalamus neurons boosted subsequent δ2-waves, specifically. δ2-dynamics paralleled that of temperature, muscle tone, heart rate, and neuronal ON-/OFF-state lengths, all reverting to characteristic NREMS levels within the first recovery hour. Thus, prolonged waking seems to necessitate a physiological recalibration before typical NREMS can be reinstated. |
format | Online Article Text |
id | pubmed-7305232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73052322020-06-26 Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep Hubbard, Jeffrey Gent, Thomas C. Hoekstra, Marieke M. B. Emmenegger, Yann Mongrain, Valerie Landolt, Hans-Peter Adamantidis, Antoine R. Franken, Paul Nat Commun Article Sleep-wake driven changes in non-rapid-eye-movement sleep (NREM) sleep (NREMS) EEG delta (δ-)power are widely used as proxy for a sleep homeostatic process. Here, we noted frequency increases in δ-waves in sleep-deprived mice, prompting us to re-evaluate how slow-wave characteristics relate to prior sleep-wake history. We identified two classes of δ-waves; one responding to sleep deprivation with high initial power and fast, discontinuous decay during recovery sleep (δ2) and another unrelated to time-spent-awake with slow, linear decay (δ1). Reanalysis of previously published datasets demonstrates that δ-band heterogeneity after sleep deprivation is also present in human subjects. Similar to sleep deprivation, silencing of centromedial thalamus neurons boosted subsequent δ2-waves, specifically. δ2-dynamics paralleled that of temperature, muscle tone, heart rate, and neuronal ON-/OFF-state lengths, all reverting to characteristic NREMS levels within the first recovery hour. Thus, prolonged waking seems to necessitate a physiological recalibration before typical NREMS can be reinstated. Nature Publishing Group UK 2020-06-19 /pmc/articles/PMC7305232/ /pubmed/32561733 http://dx.doi.org/10.1038/s41467-020-16915-0 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 Hubbard, Jeffrey Gent, Thomas C. Hoekstra, Marieke M. B. Emmenegger, Yann Mongrain, Valerie Landolt, Hans-Peter Adamantidis, Antoine R. Franken, Paul Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep |
title | Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep |
title_full | Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep |
title_fullStr | Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep |
title_full_unstemmed | Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep |
title_short | Rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in NREM sleep |
title_sort | rapid fast-delta decay following prolonged wakefulness marks a phase of wake-inertia in nrem sleep |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7305232/ https://www.ncbi.nlm.nih.gov/pubmed/32561733 http://dx.doi.org/10.1038/s41467-020-16915-0 |
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