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Timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex

Metabolic and cardiovascular processes controlled by the hindbrain exhibit 24 h rhythms, but the extent to which the hindbrain possesses endogenous circadian timekeeping is unresolved. Here we provide compelling evidence that genetic, neuronal, and vascular activities of the brainstem’s dorsal vagal...

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Autores principales: Chrobok, Lukasz, Northeast, Rebecca C., Myung, Jihwan, Cunningham, Peter S., Petit, Cheryl, Piggins, Hugh D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210107/
https://www.ncbi.nlm.nih.gov/pubmed/32385329
http://dx.doi.org/10.1038/s42003-020-0960-y
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author Chrobok, Lukasz
Northeast, Rebecca C.
Myung, Jihwan
Cunningham, Peter S.
Petit, Cheryl
Piggins, Hugh D.
author_facet Chrobok, Lukasz
Northeast, Rebecca C.
Myung, Jihwan
Cunningham, Peter S.
Petit, Cheryl
Piggins, Hugh D.
author_sort Chrobok, Lukasz
collection PubMed
description Metabolic and cardiovascular processes controlled by the hindbrain exhibit 24 h rhythms, but the extent to which the hindbrain possesses endogenous circadian timekeeping is unresolved. Here we provide compelling evidence that genetic, neuronal, and vascular activities of the brainstem’s dorsal vagal complex are subject to intrinsic circadian control with a crucial role for the connection between its components in regulating their rhythmic properties. Robust 24 h variation in clock gene expression in vivo and neuronal firing ex vivo were observed in the area postrema (AP) and nucleus of the solitary tract (NTS), together with enhanced nocturnal responsiveness to metabolic cues. Unexpectedly, we also find functional and molecular evidence for increased penetration of blood borne molecules into the NTS at night. Our findings reveal that the hindbrain houses a local network complex of neuronal and non-neuronal autonomous circadian oscillators, with clear implications for understanding local temporal control of physiology in the brainstem.
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spelling pubmed-72101072020-05-14 Timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex Chrobok, Lukasz Northeast, Rebecca C. Myung, Jihwan Cunningham, Peter S. Petit, Cheryl Piggins, Hugh D. Commun Biol Article Metabolic and cardiovascular processes controlled by the hindbrain exhibit 24 h rhythms, but the extent to which the hindbrain possesses endogenous circadian timekeeping is unresolved. Here we provide compelling evidence that genetic, neuronal, and vascular activities of the brainstem’s dorsal vagal complex are subject to intrinsic circadian control with a crucial role for the connection between its components in regulating their rhythmic properties. Robust 24 h variation in clock gene expression in vivo and neuronal firing ex vivo were observed in the area postrema (AP) and nucleus of the solitary tract (NTS), together with enhanced nocturnal responsiveness to metabolic cues. Unexpectedly, we also find functional and molecular evidence for increased penetration of blood borne molecules into the NTS at night. Our findings reveal that the hindbrain houses a local network complex of neuronal and non-neuronal autonomous circadian oscillators, with clear implications for understanding local temporal control of physiology in the brainstem. Nature Publishing Group UK 2020-05-08 /pmc/articles/PMC7210107/ /pubmed/32385329 http://dx.doi.org/10.1038/s42003-020-0960-y Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chrobok, Lukasz
Northeast, Rebecca C.
Myung, Jihwan
Cunningham, Peter S.
Petit, Cheryl
Piggins, Hugh D.
Timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex
title Timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex
title_full Timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex
title_fullStr Timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex
title_full_unstemmed Timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex
title_short Timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex
title_sort timekeeping in the hindbrain: a multi-oscillatory circadian centre in the mouse dorsal vagal complex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210107/
https://www.ncbi.nlm.nih.gov/pubmed/32385329
http://dx.doi.org/10.1038/s42003-020-0960-y
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