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Unraveling why we sleep: Quantitative analysis reveals abrupt transition from neural reorganization to repair in early development

Sleep serves disparate functions, most notably neural repair, metabolite clearance and circuit reorganization. Yet the relative importance remains hotly debated. Here, we create a novel mechanistic framework for understanding and predicting how sleep changes during ontogeny and across phylogeny. We...

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Detalles Bibliográficos
Autores principales: Cao, Junyu, Herman, Alexander B., West, Geoffrey B., Poe, Gina, Savage, Van M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500925/
https://www.ncbi.nlm.nih.gov/pubmed/32948580
http://dx.doi.org/10.1126/sciadv.aba0398
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author Cao, Junyu
Herman, Alexander B.
West, Geoffrey B.
Poe, Gina
Savage, Van M.
author_facet Cao, Junyu
Herman, Alexander B.
West, Geoffrey B.
Poe, Gina
Savage, Van M.
author_sort Cao, Junyu
collection PubMed
description Sleep serves disparate functions, most notably neural repair, metabolite clearance and circuit reorganization. Yet the relative importance remains hotly debated. Here, we create a novel mechanistic framework for understanding and predicting how sleep changes during ontogeny and across phylogeny. We use this theory to quantitatively distinguish between sleep used for neural reorganization versus repair. Our findings reveal an abrupt transition, between 2 and 3 years of age in humans. Specifically, our results show that differences in sleep across phylogeny and during late ontogeny (after 2 or 3 years in humans) are primarily due to sleep functioning for repair or clearance, while changes in sleep during early ontogeny (before 2 or 3 years) primarily support neural reorganization and learning. Moreover, our analysis shows that neuroplastic reorganization occurs primarily in REM sleep but not in NREM. This developmental transition suggests a complex interplay between developmental and evolutionary constraints on sleep.
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spelling pubmed-75009252020-09-24 Unraveling why we sleep: Quantitative analysis reveals abrupt transition from neural reorganization to repair in early development Cao, Junyu Herman, Alexander B. West, Geoffrey B. Poe, Gina Savage, Van M. Sci Adv Research Articles Sleep serves disparate functions, most notably neural repair, metabolite clearance and circuit reorganization. Yet the relative importance remains hotly debated. Here, we create a novel mechanistic framework for understanding and predicting how sleep changes during ontogeny and across phylogeny. We use this theory to quantitatively distinguish between sleep used for neural reorganization versus repair. Our findings reveal an abrupt transition, between 2 and 3 years of age in humans. Specifically, our results show that differences in sleep across phylogeny and during late ontogeny (after 2 or 3 years in humans) are primarily due to sleep functioning for repair or clearance, while changes in sleep during early ontogeny (before 2 or 3 years) primarily support neural reorganization and learning. Moreover, our analysis shows that neuroplastic reorganization occurs primarily in REM sleep but not in NREM. This developmental transition suggests a complex interplay between developmental and evolutionary constraints on sleep. American Association for the Advancement of Science 2020-09-18 /pmc/articles/PMC7500925/ /pubmed/32948580 http://dx.doi.org/10.1126/sciadv.aba0398 Text en Copyright © 2020 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). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://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
Cao, Junyu
Herman, Alexander B.
West, Geoffrey B.
Poe, Gina
Savage, Van M.
Unraveling why we sleep: Quantitative analysis reveals abrupt transition from neural reorganization to repair in early development
title Unraveling why we sleep: Quantitative analysis reveals abrupt transition from neural reorganization to repair in early development
title_full Unraveling why we sleep: Quantitative analysis reveals abrupt transition from neural reorganization to repair in early development
title_fullStr Unraveling why we sleep: Quantitative analysis reveals abrupt transition from neural reorganization to repair in early development
title_full_unstemmed Unraveling why we sleep: Quantitative analysis reveals abrupt transition from neural reorganization to repair in early development
title_short Unraveling why we sleep: Quantitative analysis reveals abrupt transition from neural reorganization to repair in early development
title_sort unraveling why we sleep: quantitative analysis reveals abrupt transition from neural reorganization to repair in early development
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500925/
https://www.ncbi.nlm.nih.gov/pubmed/32948580
http://dx.doi.org/10.1126/sciadv.aba0398
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