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A new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem
Analysis of ex vivo Per2 bioluminescent rhythm previously recorded in the mouse dorsal vagal complex reveals a characteristic phase relationship between three distinct circadian oscillators. These signals represent core clock gene expression in the area postrema (AP), the nucleus of the solitary tra...
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/PMC10073201/ https://www.ncbi.nlm.nih.gov/pubmed/37016055 http://dx.doi.org/10.1038/s41598-023-32315-y |
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author | Ahern, Jake Chrobok, Łukasz Champneys, Alan R. Piggins, Hugh D. |
author_facet | Ahern, Jake Chrobok, Łukasz Champneys, Alan R. Piggins, Hugh D. |
author_sort | Ahern, Jake |
collection | PubMed |
description | Analysis of ex vivo Per2 bioluminescent rhythm previously recorded in the mouse dorsal vagal complex reveals a characteristic phase relationship between three distinct circadian oscillators. These signals represent core clock gene expression in the area postrema (AP), the nucleus of the solitary tract (NTS) and the ependymal cells surrounding the 4th ventricle (4Vep). Initially, the data suggests a consistent phasing in which the AP peaks first, followed shortly by the NTS, with the 4Vep peaking 8–9 h later. Wavelet analysis reveals that this pattern is not consistently maintained throughout a recording, however, the phase dynamics strongly imply that oscillator interactions are present. A simple phase model of the three oscillators is developed and it suggests that realistic phase dynamics occur between three model oscillators with coupling close to a synchronisation transition. The coupling topology suggests that the AP bidirectionally communicates phase information to the NTS and the 4Vep to synchronise the three structures. A comparison of the model with previous experimental manipulations demonstrates its feasibility to explain DVC circadian phasing. Finally, we show that simulating steadily decaying coupling improves the model’s ability to capture experimental phase dynamics. |
format | Online Article Text |
id | pubmed-10073201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100732012023-04-06 A new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem Ahern, Jake Chrobok, Łukasz Champneys, Alan R. Piggins, Hugh D. Sci Rep Article Analysis of ex vivo Per2 bioluminescent rhythm previously recorded in the mouse dorsal vagal complex reveals a characteristic phase relationship between three distinct circadian oscillators. These signals represent core clock gene expression in the area postrema (AP), the nucleus of the solitary tract (NTS) and the ependymal cells surrounding the 4th ventricle (4Vep). Initially, the data suggests a consistent phasing in which the AP peaks first, followed shortly by the NTS, with the 4Vep peaking 8–9 h later. Wavelet analysis reveals that this pattern is not consistently maintained throughout a recording, however, the phase dynamics strongly imply that oscillator interactions are present. A simple phase model of the three oscillators is developed and it suggests that realistic phase dynamics occur between three model oscillators with coupling close to a synchronisation transition. The coupling topology suggests that the AP bidirectionally communicates phase information to the NTS and the 4Vep to synchronise the three structures. A comparison of the model with previous experimental manipulations demonstrates its feasibility to explain DVC circadian phasing. Finally, we show that simulating steadily decaying coupling improves the model’s ability to capture experimental phase dynamics. Nature Publishing Group UK 2023-04-04 /pmc/articles/PMC10073201/ /pubmed/37016055 http://dx.doi.org/10.1038/s41598-023-32315-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Ahern, Jake Chrobok, Łukasz Champneys, Alan R. Piggins, Hugh D. A new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem |
title | A new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem |
title_full | A new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem |
title_fullStr | A new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem |
title_full_unstemmed | A new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem |
title_short | A new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem |
title_sort | new phase model of the spatiotemporal relationships between three circadian oscillators in the brainstem |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073201/ https://www.ncbi.nlm.nih.gov/pubmed/37016055 http://dx.doi.org/10.1038/s41598-023-32315-y |
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