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Coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep
Rodents sleep in bouts lasting minutes; humans sleep for hours. What are the universal needs served by sleep given such variability? In sleeping mice and humans, through monitoring neural and cardiac activity (combined with assessment of arousability and overnight memory consolidation, respectively)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5298853/ https://www.ncbi.nlm.nih.gov/pubmed/28246641 http://dx.doi.org/10.1126/sciadv.1602026 |
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author | Lecci, Sandro Fernandez, Laura M. J. Weber, Frederik D. Cardis, Romain Chatton, Jean-Yves Born, Jan Lüthi, Anita |
author_facet | Lecci, Sandro Fernandez, Laura M. J. Weber, Frederik D. Cardis, Romain Chatton, Jean-Yves Born, Jan Lüthi, Anita |
author_sort | Lecci, Sandro |
collection | PubMed |
description | Rodents sleep in bouts lasting minutes; humans sleep for hours. What are the universal needs served by sleep given such variability? In sleeping mice and humans, through monitoring neural and cardiac activity (combined with assessment of arousability and overnight memory consolidation, respectively), we find a previously unrecognized hallmark of sleep that balances two fundamental yet opposing needs: to maintain sensory reactivity to the environment while promoting recovery and memory consolidation. Coordinated 0.02-Hz oscillations of the sleep spindle band, hippocampal ripple activity, and heart rate sequentially divide non–rapid eye movement (non-REM) sleep into offline phases and phases of high susceptibility to external stimulation. A noise stimulus chosen such that sleeping mice woke up or slept through at comparable rates revealed that offline periods correspond to raising, whereas fragility periods correspond to declining portions of the 0.02-Hz oscillation in spindle activity. Oscillations were present throughout non-REM sleep in mice, yet confined to light non-REM sleep (stage 2) in humans. In both species, the 0.02-Hz oscillation predominated over posterior cortex. The strength of the 0.02-Hz oscillation predicted superior memory recall after sleep in a declarative memory task in humans. These oscillations point to a conserved function of mammalian non-REM sleep that cycles between environmental alertness and internal memory processing in 20- to 25-s intervals. Perturbed 0.02-Hz oscillations may cause memory impairment and ill-timed arousals in sleep disorders. |
format | Online Article Text |
id | pubmed-5298853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52988532017-02-28 Coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep Lecci, Sandro Fernandez, Laura M. J. Weber, Frederik D. Cardis, Romain Chatton, Jean-Yves Born, Jan Lüthi, Anita Sci Adv Research Articles Rodents sleep in bouts lasting minutes; humans sleep for hours. What are the universal needs served by sleep given such variability? In sleeping mice and humans, through monitoring neural and cardiac activity (combined with assessment of arousability and overnight memory consolidation, respectively), we find a previously unrecognized hallmark of sleep that balances two fundamental yet opposing needs: to maintain sensory reactivity to the environment while promoting recovery and memory consolidation. Coordinated 0.02-Hz oscillations of the sleep spindle band, hippocampal ripple activity, and heart rate sequentially divide non–rapid eye movement (non-REM) sleep into offline phases and phases of high susceptibility to external stimulation. A noise stimulus chosen such that sleeping mice woke up or slept through at comparable rates revealed that offline periods correspond to raising, whereas fragility periods correspond to declining portions of the 0.02-Hz oscillation in spindle activity. Oscillations were present throughout non-REM sleep in mice, yet confined to light non-REM sleep (stage 2) in humans. In both species, the 0.02-Hz oscillation predominated over posterior cortex. The strength of the 0.02-Hz oscillation predicted superior memory recall after sleep in a declarative memory task in humans. These oscillations point to a conserved function of mammalian non-REM sleep that cycles between environmental alertness and internal memory processing in 20- to 25-s intervals. Perturbed 0.02-Hz oscillations may cause memory impairment and ill-timed arousals in sleep disorders. American Association for the Advancement of Science 2017-02-08 /pmc/articles/PMC5298853/ /pubmed/28246641 http://dx.doi.org/10.1126/sciadv.1602026 Text en Copyright © 2017, The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Lecci, Sandro Fernandez, Laura M. J. Weber, Frederik D. Cardis, Romain Chatton, Jean-Yves Born, Jan Lüthi, Anita Coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep |
title | Coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep |
title_full | Coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep |
title_fullStr | Coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep |
title_full_unstemmed | Coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep |
title_short | Coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep |
title_sort | coordinated infraslow neural and cardiac oscillations mark fragility and offline periods in mammalian sleep |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5298853/ https://www.ncbi.nlm.nih.gov/pubmed/28246641 http://dx.doi.org/10.1126/sciadv.1602026 |
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