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Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome
In addition to regular sleep/wake cycles, humans and animals exhibit brief arousals from sleep. Although much is known about consolidated sleep and wakefulness, the mechanism that triggers arousals remains enigmatic. Here, we argue that arousals are caused by the intrinsic neuronal noise of wake-pro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916514/ https://www.ncbi.nlm.nih.gov/pubmed/29707639 http://dx.doi.org/10.1126/sciadv.aar6277 |
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author | Dvir, Hila Elbaz, Idan Havlin, Shlomo Appelbaum, Lior Ivanov, Plamen Ch. Bartsch, Ronny P. |
author_facet | Dvir, Hila Elbaz, Idan Havlin, Shlomo Appelbaum, Lior Ivanov, Plamen Ch. Bartsch, Ronny P. |
author_sort | Dvir, Hila |
collection | PubMed |
description | In addition to regular sleep/wake cycles, humans and animals exhibit brief arousals from sleep. Although much is known about consolidated sleep and wakefulness, the mechanism that triggers arousals remains enigmatic. Here, we argue that arousals are caused by the intrinsic neuronal noise of wake-promoting neurons. We propose a model that simulates the superposition of the noise from a group of neurons, and show that, occasionally, the superposed noise exceeds the excitability threshold and provokes an arousal. Because neuronal noise decreases with increasing temperature, our model predicts arousal frequency to decrease as well. To test this prediction, we perform experiments on the sleep/wake behavior of zebrafish larvae and find that increasing water temperatures lead to fewer and shorter arousals, as predicted by our analytic derivations and model simulations. Our findings indicate a previously unrecognized neurophysiological mechanism that links sleep arousals with temperature regulation, and may explain the origin of the clinically observed higher risk for sudden infant death syndrome with increased ambient temperature. |
format | Online Article Text |
id | pubmed-5916514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59165142018-04-27 Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome Dvir, Hila Elbaz, Idan Havlin, Shlomo Appelbaum, Lior Ivanov, Plamen Ch. Bartsch, Ronny P. Sci Adv Research Articles In addition to regular sleep/wake cycles, humans and animals exhibit brief arousals from sleep. Although much is known about consolidated sleep and wakefulness, the mechanism that triggers arousals remains enigmatic. Here, we argue that arousals are caused by the intrinsic neuronal noise of wake-promoting neurons. We propose a model that simulates the superposition of the noise from a group of neurons, and show that, occasionally, the superposed noise exceeds the excitability threshold and provokes an arousal. Because neuronal noise decreases with increasing temperature, our model predicts arousal frequency to decrease as well. To test this prediction, we perform experiments on the sleep/wake behavior of zebrafish larvae and find that increasing water temperatures lead to fewer and shorter arousals, as predicted by our analytic derivations and model simulations. Our findings indicate a previously unrecognized neurophysiological mechanism that links sleep arousals with temperature regulation, and may explain the origin of the clinically observed higher risk for sudden infant death syndrome with increased ambient temperature. American Association for the Advancement of Science 2018-04-25 /pmc/articles/PMC5916514/ /pubmed/29707639 http://dx.doi.org/10.1126/sciadv.aar6277 Text en Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Dvir, Hila Elbaz, Idan Havlin, Shlomo Appelbaum, Lior Ivanov, Plamen Ch. Bartsch, Ronny P. Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome |
title | Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome |
title_full | Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome |
title_fullStr | Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome |
title_full_unstemmed | Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome |
title_short | Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome |
title_sort | neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916514/ https://www.ncbi.nlm.nih.gov/pubmed/29707639 http://dx.doi.org/10.1126/sciadv.aar6277 |
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