Cargando…

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)...

Descripción completa

Detalles Bibliográficos
Autores principales: Lecci, Sandro, Fernandez, Laura M. J., Weber, Frederik D., Cardis, Romain, Chatton, Jean-Yves, Born, Jan, Lüthi, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2017
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
_version_ 1782505935023898624
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
work_keys_str_mv AT leccisandro coordinatedinfraslowneuralandcardiacoscillationsmarkfragilityandofflineperiodsinmammaliansleep
AT fernandezlauramj coordinatedinfraslowneuralandcardiacoscillationsmarkfragilityandofflineperiodsinmammaliansleep
AT weberfrederikd coordinatedinfraslowneuralandcardiacoscillationsmarkfragilityandofflineperiodsinmammaliansleep
AT cardisromain coordinatedinfraslowneuralandcardiacoscillationsmarkfragilityandofflineperiodsinmammaliansleep
AT chattonjeanyves coordinatedinfraslowneuralandcardiacoscillationsmarkfragilityandofflineperiodsinmammaliansleep
AT bornjan coordinatedinfraslowneuralandcardiacoscillationsmarkfragilityandofflineperiodsinmammaliansleep
AT luthianita coordinatedinfraslowneuralandcardiacoscillationsmarkfragilityandofflineperiodsinmammaliansleep