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Assessment of Sleep, K-Complexes, and Sleep Spindles in a T21 Light-Dark Cycle

Circadian rhythm misalignment has a deleterious impact on the brain and the body. In rats, exposure to a 21-hour day length impairs hippocampal dependent memory. Sleep, and particularly K-complexes and sleep spindles in the cortex, have been hypothesized to be involved in memory consolidation. Alter...

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Autores principales: Deibel, Scott H., Rota, Ryan, Steenland, Hendrik W., Ali, Karim, McNaughton, Bruce L., Tatsuno, Masami, McDonald, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573124/
https://www.ncbi.nlm.nih.gov/pubmed/33122986
http://dx.doi.org/10.3389/fnins.2020.551843
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author Deibel, Scott H.
Rota, Ryan
Steenland, Hendrik W.
Ali, Karim
McNaughton, Bruce L.
Tatsuno, Masami
McDonald, Robert J.
author_facet Deibel, Scott H.
Rota, Ryan
Steenland, Hendrik W.
Ali, Karim
McNaughton, Bruce L.
Tatsuno, Masami
McDonald, Robert J.
author_sort Deibel, Scott H.
collection PubMed
description Circadian rhythm misalignment has a deleterious impact on the brain and the body. In rats, exposure to a 21-hour day length impairs hippocampal dependent memory. Sleep, and particularly K-complexes and sleep spindles in the cortex, have been hypothesized to be involved in memory consolidation. Altered K-complexes, sleep spindles, or interaction between the cortex and hippocampus could be a mechanism for the memory consolidation failure but has yet to be assessed in any circadian misalignment paradigm. In the current study, continuous local field potential recordings from five rats were used to assess the changes in aspects of behavior and sleep, including wheel running activity, quiet wakefulness, motionless sleep, slow wave sleep, REM sleep, K-complexes and sleep spindles, in rats exposed to six consecutive days of a T21 light-dark cycle (L9:D12). Except for a temporal redistribution of sleep and activity during the T21, there were no changes in period, or total amount for any aspect of sleep or activity. These data suggest that the memory impairment elicited from 6 days of T21 exposure is likely not due to changes in sleep architecture. It remains possible that hippocampal plasticity is affected by experiencing light when subjective circadian phase is calling for dark. However, if there is a reduction in hippocampal plasticity, changes in sleep appear not to be driving this effect.
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spelling pubmed-75731242020-10-28 Assessment of Sleep, K-Complexes, and Sleep Spindles in a T21 Light-Dark Cycle Deibel, Scott H. Rota, Ryan Steenland, Hendrik W. Ali, Karim McNaughton, Bruce L. Tatsuno, Masami McDonald, Robert J. Front Neurosci Neuroscience Circadian rhythm misalignment has a deleterious impact on the brain and the body. In rats, exposure to a 21-hour day length impairs hippocampal dependent memory. Sleep, and particularly K-complexes and sleep spindles in the cortex, have been hypothesized to be involved in memory consolidation. Altered K-complexes, sleep spindles, or interaction between the cortex and hippocampus could be a mechanism for the memory consolidation failure but has yet to be assessed in any circadian misalignment paradigm. In the current study, continuous local field potential recordings from five rats were used to assess the changes in aspects of behavior and sleep, including wheel running activity, quiet wakefulness, motionless sleep, slow wave sleep, REM sleep, K-complexes and sleep spindles, in rats exposed to six consecutive days of a T21 light-dark cycle (L9:D12). Except for a temporal redistribution of sleep and activity during the T21, there were no changes in period, or total amount for any aspect of sleep or activity. These data suggest that the memory impairment elicited from 6 days of T21 exposure is likely not due to changes in sleep architecture. It remains possible that hippocampal plasticity is affected by experiencing light when subjective circadian phase is calling for dark. However, if there is a reduction in hippocampal plasticity, changes in sleep appear not to be driving this effect. Frontiers Media S.A. 2020-10-06 /pmc/articles/PMC7573124/ /pubmed/33122986 http://dx.doi.org/10.3389/fnins.2020.551843 Text en Copyright © 2020 Deibel, Rota, Steenland, Ali, McNaughton, Tatsuno and McDonald. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Deibel, Scott H.
Rota, Ryan
Steenland, Hendrik W.
Ali, Karim
McNaughton, Bruce L.
Tatsuno, Masami
McDonald, Robert J.
Assessment of Sleep, K-Complexes, and Sleep Spindles in a T21 Light-Dark Cycle
title Assessment of Sleep, K-Complexes, and Sleep Spindles in a T21 Light-Dark Cycle
title_full Assessment of Sleep, K-Complexes, and Sleep Spindles in a T21 Light-Dark Cycle
title_fullStr Assessment of Sleep, K-Complexes, and Sleep Spindles in a T21 Light-Dark Cycle
title_full_unstemmed Assessment of Sleep, K-Complexes, and Sleep Spindles in a T21 Light-Dark Cycle
title_short Assessment of Sleep, K-Complexes, and Sleep Spindles in a T21 Light-Dark Cycle
title_sort assessment of sleep, k-complexes, and sleep spindles in a t21 light-dark cycle
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573124/
https://www.ncbi.nlm.nih.gov/pubmed/33122986
http://dx.doi.org/10.3389/fnins.2020.551843
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