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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...

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Autores principales: Hubbard, Jeffrey, Gent, Thomas C., Hoekstra, Marieke M. B., Emmenegger, Yann, Mongrain, Valerie, Landolt, Hans-Peter, Adamantidis, Antoine R., Franken, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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.
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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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