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Early life circadian rhythm disruption in mice alters brain and behavior in adulthood
Healthy sleep supports robust development of the brain and behavior. Modern society presents a host of challenges that can impair and disrupt critical circadian rhythms that reinforce optimal physiological functioning, including the proper timing and consolidation of sleep. While the acute effects o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072337/ https://www.ncbi.nlm.nih.gov/pubmed/35513413 http://dx.doi.org/10.1038/s41598-022-11335-0 |
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author | Ameen, Rafal W. Warshawski, Allison Fu, Lucia Antle, Michael C. |
author_facet | Ameen, Rafal W. Warshawski, Allison Fu, Lucia Antle, Michael C. |
author_sort | Ameen, Rafal W. |
collection | PubMed |
description | Healthy sleep supports robust development of the brain and behavior. Modern society presents a host of challenges that can impair and disrupt critical circadian rhythms that reinforce optimal physiological functioning, including the proper timing and consolidation of sleep. While the acute effects of inadequate sleep and disrupted circadian rhythms are being defined, the adverse developmental consequences of disrupted sleep and circadian rhythms are understudied. Here, we exposed mice to disrupting light–dark cycles from birth until weaning and demonstrate that such exposure has adverse impacts on brain and behavior as adults. Mice that experience early-life circadian disruption exhibit more anxiety-like behavior in the elevated plus maze, poorer spatial memory in the Morris Water Maze, and impaired working memory in a delayed match-to-sample task. Additionally, neuron morphology in the amygdala, hippocampus and prefrontal cortex is adversely impacted. Pyramidal cells in these areas had smaller dendritic fields, and pyramidal cells in the prefrontal cortex and hippocampus also exhibited diminished branching orders. Disrupted mice were also hyperactive as adults, but otherwise exhibited no alteration in adult circadian locomotor rhythms. These results highlight that circadian disruption early in life may have long lasting and far-reaching consequences for the development of behavior and the brain. |
format | Online Article Text |
id | pubmed-9072337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90723372022-05-07 Early life circadian rhythm disruption in mice alters brain and behavior in adulthood Ameen, Rafal W. Warshawski, Allison Fu, Lucia Antle, Michael C. Sci Rep Article Healthy sleep supports robust development of the brain and behavior. Modern society presents a host of challenges that can impair and disrupt critical circadian rhythms that reinforce optimal physiological functioning, including the proper timing and consolidation of sleep. While the acute effects of inadequate sleep and disrupted circadian rhythms are being defined, the adverse developmental consequences of disrupted sleep and circadian rhythms are understudied. Here, we exposed mice to disrupting light–dark cycles from birth until weaning and demonstrate that such exposure has adverse impacts on brain and behavior as adults. Mice that experience early-life circadian disruption exhibit more anxiety-like behavior in the elevated plus maze, poorer spatial memory in the Morris Water Maze, and impaired working memory in a delayed match-to-sample task. Additionally, neuron morphology in the amygdala, hippocampus and prefrontal cortex is adversely impacted. Pyramidal cells in these areas had smaller dendritic fields, and pyramidal cells in the prefrontal cortex and hippocampus also exhibited diminished branching orders. Disrupted mice were also hyperactive as adults, but otherwise exhibited no alteration in adult circadian locomotor rhythms. These results highlight that circadian disruption early in life may have long lasting and far-reaching consequences for the development of behavior and the brain. Nature Publishing Group UK 2022-05-05 /pmc/articles/PMC9072337/ /pubmed/35513413 http://dx.doi.org/10.1038/s41598-022-11335-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ameen, Rafal W. Warshawski, Allison Fu, Lucia Antle, Michael C. Early life circadian rhythm disruption in mice alters brain and behavior in adulthood |
title | Early life circadian rhythm disruption in mice alters brain and behavior in adulthood |
title_full | Early life circadian rhythm disruption in mice alters brain and behavior in adulthood |
title_fullStr | Early life circadian rhythm disruption in mice alters brain and behavior in adulthood |
title_full_unstemmed | Early life circadian rhythm disruption in mice alters brain and behavior in adulthood |
title_short | Early life circadian rhythm disruption in mice alters brain and behavior in adulthood |
title_sort | early life circadian rhythm disruption in mice alters brain and behavior in adulthood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072337/ https://www.ncbi.nlm.nih.gov/pubmed/35513413 http://dx.doi.org/10.1038/s41598-022-11335-0 |
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