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Temperature-robust rapid eye movement and slow wave sleep in the lizard Laudakia vulgaris

During sleep our brain switches between two starkly different brain states - slow wave sleep (SWS) and rapid eye movement (REM) sleep. While this two-state sleep pattern is abundant across birds and mammals, its existence in other vertebrates is not universally accepted, its evolutionary emergence i...

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Autores principales: Albeck, Nitzan, Udi, Daniel I., Eyal, Regev, Shvartsman, Arik, Shein-Idelson, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709036/
https://www.ncbi.nlm.nih.gov/pubmed/36446903
http://dx.doi.org/10.1038/s42003-022-04261-4
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author Albeck, Nitzan
Udi, Daniel I.
Eyal, Regev
Shvartsman, Arik
Shein-Idelson, Mark
author_facet Albeck, Nitzan
Udi, Daniel I.
Eyal, Regev
Shvartsman, Arik
Shein-Idelson, Mark
author_sort Albeck, Nitzan
collection PubMed
description During sleep our brain switches between two starkly different brain states - slow wave sleep (SWS) and rapid eye movement (REM) sleep. While this two-state sleep pattern is abundant across birds and mammals, its existence in other vertebrates is not universally accepted, its evolutionary emergence is unclear and it is undetermined whether it is a fundamental property of vertebrate brains or an adaptation specific to homeotherms. To address these questions, we conducted electrophysiological recordings in the Agamid lizard, Laudakia vulgaris during sleep. We found clear signatures of two-state sleep that resemble the mammalian and avian sleep patterns. These states switched periodically throughout the night with a cycle of ~90 seconds and were remarkably similar to the states previously reported in Pogona vitticeps. Interestingly, in contrast to the high temperature sensitivity of mammalian states, state switches were robust to large variations in temperature. We also found that breathing rate, micro-movements and eye movements were locked to the REM state as they are in mammals. Collectively, these findings suggest that two-state sleep is abundant across the agamid family, shares physiological similarity to mammalian sleep, and can be maintain in poikilothems, increasing the probability that it existed in the cold-blooded ancestor of amniotes.
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spelling pubmed-97090362022-12-01 Temperature-robust rapid eye movement and slow wave sleep in the lizard Laudakia vulgaris Albeck, Nitzan Udi, Daniel I. Eyal, Regev Shvartsman, Arik Shein-Idelson, Mark Commun Biol Article During sleep our brain switches between two starkly different brain states - slow wave sleep (SWS) and rapid eye movement (REM) sleep. While this two-state sleep pattern is abundant across birds and mammals, its existence in other vertebrates is not universally accepted, its evolutionary emergence is unclear and it is undetermined whether it is a fundamental property of vertebrate brains or an adaptation specific to homeotherms. To address these questions, we conducted electrophysiological recordings in the Agamid lizard, Laudakia vulgaris during sleep. We found clear signatures of two-state sleep that resemble the mammalian and avian sleep patterns. These states switched periodically throughout the night with a cycle of ~90 seconds and were remarkably similar to the states previously reported in Pogona vitticeps. Interestingly, in contrast to the high temperature sensitivity of mammalian states, state switches were robust to large variations in temperature. We also found that breathing rate, micro-movements and eye movements were locked to the REM state as they are in mammals. Collectively, these findings suggest that two-state sleep is abundant across the agamid family, shares physiological similarity to mammalian sleep, and can be maintain in poikilothems, increasing the probability that it existed in the cold-blooded ancestor of amniotes. Nature Publishing Group UK 2022-11-29 /pmc/articles/PMC9709036/ /pubmed/36446903 http://dx.doi.org/10.1038/s42003-022-04261-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Albeck, Nitzan
Udi, Daniel I.
Eyal, Regev
Shvartsman, Arik
Shein-Idelson, Mark
Temperature-robust rapid eye movement and slow wave sleep in the lizard Laudakia vulgaris
title Temperature-robust rapid eye movement and slow wave sleep in the lizard Laudakia vulgaris
title_full Temperature-robust rapid eye movement and slow wave sleep in the lizard Laudakia vulgaris
title_fullStr Temperature-robust rapid eye movement and slow wave sleep in the lizard Laudakia vulgaris
title_full_unstemmed Temperature-robust rapid eye movement and slow wave sleep in the lizard Laudakia vulgaris
title_short Temperature-robust rapid eye movement and slow wave sleep in the lizard Laudakia vulgaris
title_sort temperature-robust rapid eye movement and slow wave sleep in the lizard laudakia vulgaris
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709036/
https://www.ncbi.nlm.nih.gov/pubmed/36446903
http://dx.doi.org/10.1038/s42003-022-04261-4
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