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Daily Torpor and Sleep in a Non-human Primate, the Gray Mouse Lemur (Microcebus murinus)

Daily torpor is an energy-saving process that evolved as an extension of non-rapid eye movement (NREM) sleep mechanisms. In many heterothermic species there is a relation between torpor expression and the repartition of the different behavioral states of sleep. Despite the presence of sleep during t...

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Autores principales: Royo, Julie, Aujard, Fabienne, Pifferi, Fabien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768945/
https://www.ncbi.nlm.nih.gov/pubmed/31616258
http://dx.doi.org/10.3389/fnana.2019.00087
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author Royo, Julie
Aujard, Fabienne
Pifferi, Fabien
author_facet Royo, Julie
Aujard, Fabienne
Pifferi, Fabien
author_sort Royo, Julie
collection PubMed
description Daily torpor is an energy-saving process that evolved as an extension of non-rapid eye movement (NREM) sleep mechanisms. In many heterothermic species there is a relation between torpor expression and the repartition of the different behavioral states of sleep. Despite the presence of sleep during this period of hypothermia, torpor induces an accumulation of sleep debt which results in a rebound of sleep in mammals. We aimed to investigate the expression of sleep-wake rhythms and delta waves during daily torpor at various ambient temperatures in a non-human primate model, the gray mouse lemur (Microcebus murinus). Cortical activity was measured with telemetric electroencephalography (EEG) recordings in the prefrontal cortex (PFC) during the torpor episode and the next 24 h following hypothermia. Gray mouse lemurs were divided into two groups: the first group was subjected to normal ambient temperatures (25°C) whereas the second group was placed at lower ambient temperatures (10°C). Contrary to normal ambient temperatures, sleep-wake rhythms were maintained during torpor until body temperature (Tb) of the animals reached 21°C. Below this temperature, NREM and REM sleep strongly decreased or were absent whereas the EEG became isoelectric. The different states of sleep were proportional to Tb(min) during prior torpor in contrast to active phases. Delta waves increased after torpor but low Tb did not induce greater delta power compared to higher temperatures. Our results showed that Tb was a determining factor for the quality and quantity of sleep. Low Tb might be inconsistent with the recovery function of sleep. Heterothermy caused a sleep debt thus there was a rebound of sleep at the beginning of euthermia to compensate for the lack of sleep.
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spelling pubmed-67689452019-10-15 Daily Torpor and Sleep in a Non-human Primate, the Gray Mouse Lemur (Microcebus murinus) Royo, Julie Aujard, Fabienne Pifferi, Fabien Front Neuroanat Neuroscience Daily torpor is an energy-saving process that evolved as an extension of non-rapid eye movement (NREM) sleep mechanisms. In many heterothermic species there is a relation between torpor expression and the repartition of the different behavioral states of sleep. Despite the presence of sleep during this period of hypothermia, torpor induces an accumulation of sleep debt which results in a rebound of sleep in mammals. We aimed to investigate the expression of sleep-wake rhythms and delta waves during daily torpor at various ambient temperatures in a non-human primate model, the gray mouse lemur (Microcebus murinus). Cortical activity was measured with telemetric electroencephalography (EEG) recordings in the prefrontal cortex (PFC) during the torpor episode and the next 24 h following hypothermia. Gray mouse lemurs were divided into two groups: the first group was subjected to normal ambient temperatures (25°C) whereas the second group was placed at lower ambient temperatures (10°C). Contrary to normal ambient temperatures, sleep-wake rhythms were maintained during torpor until body temperature (Tb) of the animals reached 21°C. Below this temperature, NREM and REM sleep strongly decreased or were absent whereas the EEG became isoelectric. The different states of sleep were proportional to Tb(min) during prior torpor in contrast to active phases. Delta waves increased after torpor but low Tb did not induce greater delta power compared to higher temperatures. Our results showed that Tb was a determining factor for the quality and quantity of sleep. Low Tb might be inconsistent with the recovery function of sleep. Heterothermy caused a sleep debt thus there was a rebound of sleep at the beginning of euthermia to compensate for the lack of sleep. Frontiers Media S.A. 2019-09-24 /pmc/articles/PMC6768945/ /pubmed/31616258 http://dx.doi.org/10.3389/fnana.2019.00087 Text en Copyright © 2019 Royo, Aujard and Pifferi. 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
Royo, Julie
Aujard, Fabienne
Pifferi, Fabien
Daily Torpor and Sleep in a Non-human Primate, the Gray Mouse Lemur (Microcebus murinus)
title Daily Torpor and Sleep in a Non-human Primate, the Gray Mouse Lemur (Microcebus murinus)
title_full Daily Torpor and Sleep in a Non-human Primate, the Gray Mouse Lemur (Microcebus murinus)
title_fullStr Daily Torpor and Sleep in a Non-human Primate, the Gray Mouse Lemur (Microcebus murinus)
title_full_unstemmed Daily Torpor and Sleep in a Non-human Primate, the Gray Mouse Lemur (Microcebus murinus)
title_short Daily Torpor and Sleep in a Non-human Primate, the Gray Mouse Lemur (Microcebus murinus)
title_sort daily torpor and sleep in a non-human primate, the gray mouse lemur (microcebus murinus)
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6768945/
https://www.ncbi.nlm.nih.gov/pubmed/31616258
http://dx.doi.org/10.3389/fnana.2019.00087
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