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Circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice
Disruption of circadian rhythms, such as shift work and jet lag, are associated with negative physiological and behavioral outcomes, including changes in affective state, learning and memory, and cognitive function. The prefrontal cortex (PFC) is heavily involved in all of these processes. Many PFC-...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244337/ https://www.ncbi.nlm.nih.gov/pubmed/37280307 http://dx.doi.org/10.1038/s41598-023-35898-8 |
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author | Roberts, Brandon L. Karatsoreos, Ilia N. |
author_facet | Roberts, Brandon L. Karatsoreos, Ilia N. |
author_sort | Roberts, Brandon L. |
collection | PubMed |
description | Disruption of circadian rhythms, such as shift work and jet lag, are associated with negative physiological and behavioral outcomes, including changes in affective state, learning and memory, and cognitive function. The prefrontal cortex (PFC) is heavily involved in all of these processes. Many PFC-associated behaviors are time-of-day dependent, and disruption of daily rhythms negatively impacts these behavioral outputs. Yet how disruption of daily rhythms impacts the fundamental function of PFC neurons, and the mechanism(s) by which this occurs, remains unknown. Using a mouse model, we demonstrate that the activity and action potential dynamics of prelimbic PFC neurons are regulated by time-of-day in a sex specific manner. Further, we show that postsynaptic K(+) channels play a central role in physiological rhythms, suggesting an intrinsic gating mechanism mediating physiological activity. Finally, we demonstrate that environmental circadian desynchronization alters the intrinsic functioning of these neurons independent of time-of-day. These key discoveries demonstrate that daily rhythms contribute to the mechanisms underlying the essential physiology of PFC circuits and provide potential mechanisms by which circadian disruption may impact the fundamental properties of neurons. |
format | Online Article Text |
id | pubmed-10244337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102443372023-06-08 Circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice Roberts, Brandon L. Karatsoreos, Ilia N. Sci Rep Article Disruption of circadian rhythms, such as shift work and jet lag, are associated with negative physiological and behavioral outcomes, including changes in affective state, learning and memory, and cognitive function. The prefrontal cortex (PFC) is heavily involved in all of these processes. Many PFC-associated behaviors are time-of-day dependent, and disruption of daily rhythms negatively impacts these behavioral outputs. Yet how disruption of daily rhythms impacts the fundamental function of PFC neurons, and the mechanism(s) by which this occurs, remains unknown. Using a mouse model, we demonstrate that the activity and action potential dynamics of prelimbic PFC neurons are regulated by time-of-day in a sex specific manner. Further, we show that postsynaptic K(+) channels play a central role in physiological rhythms, suggesting an intrinsic gating mechanism mediating physiological activity. Finally, we demonstrate that environmental circadian desynchronization alters the intrinsic functioning of these neurons independent of time-of-day. These key discoveries demonstrate that daily rhythms contribute to the mechanisms underlying the essential physiology of PFC circuits and provide potential mechanisms by which circadian disruption may impact the fundamental properties of neurons. Nature Publishing Group UK 2023-06-06 /pmc/articles/PMC10244337/ /pubmed/37280307 http://dx.doi.org/10.1038/s41598-023-35898-8 Text en © The Author(s) 2023 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 Roberts, Brandon L. Karatsoreos, Ilia N. Circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice |
title | Circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice |
title_full | Circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice |
title_fullStr | Circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice |
title_full_unstemmed | Circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice |
title_short | Circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice |
title_sort | circadian desynchronization disrupts physiological rhythms of prefrontal cortex pyramidal neurons in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244337/ https://www.ncbi.nlm.nih.gov/pubmed/37280307 http://dx.doi.org/10.1038/s41598-023-35898-8 |
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