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Suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice
Searching for food follows a well-organized decision process in mammals to take up food only if necessary. Moreover, scavenging is preferred during their activity phase. Various time-dependent regulatory processes have been identified originating from the suprachiasmatic nuclei (SCN), which convert...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582613/ https://www.ncbi.nlm.nih.gov/pubmed/36277219 http://dx.doi.org/10.3389/fphys.2022.909795 |
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author | Olejniczak, Iwona Campbell, Benjamin Tsai, Yuan-Chen Tyagarajan, Shiva K. Albrecht, Urs Ripperger, Jürgen A. |
author_facet | Olejniczak, Iwona Campbell, Benjamin Tsai, Yuan-Chen Tyagarajan, Shiva K. Albrecht, Urs Ripperger, Jürgen A. |
author_sort | Olejniczak, Iwona |
collection | PubMed |
description | Searching for food follows a well-organized decision process in mammals to take up food only if necessary. Moreover, scavenging is preferred during their activity phase. Various time-dependent regulatory processes have been identified originating from the suprachiasmatic nuclei (SCN), which convert external light information into synchronizing output signals. However, a direct impact of the SCN on the timing of normal food searching has not yet been found. Here, we revisited the function of the SCN to affect when mice look for food. We found that this process was independent of light but modified by the palatability of the food source. Surprisingly, reducing the output from the SCN, in particular from the vasopressin releasing neurons, reduced the amount of scavenging during the early activity phase. The SCN appeared to transmit a signal to the paraventricular nuclei (PVN) via GABA receptor A1. Finally, the interaction of SCN and PVN was verified by retrograde transport-mediated complementation. None of the genetic manipulations affected the uptake of more palatable food. The data indicate that the PVN are sufficient to produce blunted food searching rhythms and are responsive to hedonistic feeding. Nevertheless, the search for normal food during the early activity phase is significantly enhanced by the SCN. |
format | Online Article Text |
id | pubmed-9582613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95826132022-10-21 Suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice Olejniczak, Iwona Campbell, Benjamin Tsai, Yuan-Chen Tyagarajan, Shiva K. Albrecht, Urs Ripperger, Jürgen A. Front Physiol Physiology Searching for food follows a well-organized decision process in mammals to take up food only if necessary. Moreover, scavenging is preferred during their activity phase. Various time-dependent regulatory processes have been identified originating from the suprachiasmatic nuclei (SCN), which convert external light information into synchronizing output signals. However, a direct impact of the SCN on the timing of normal food searching has not yet been found. Here, we revisited the function of the SCN to affect when mice look for food. We found that this process was independent of light but modified by the palatability of the food source. Surprisingly, reducing the output from the SCN, in particular from the vasopressin releasing neurons, reduced the amount of scavenging during the early activity phase. The SCN appeared to transmit a signal to the paraventricular nuclei (PVN) via GABA receptor A1. Finally, the interaction of SCN and PVN was verified by retrograde transport-mediated complementation. None of the genetic manipulations affected the uptake of more palatable food. The data indicate that the PVN are sufficient to produce blunted food searching rhythms and are responsive to hedonistic feeding. Nevertheless, the search for normal food during the early activity phase is significantly enhanced by the SCN. Frontiers Media S.A. 2022-10-06 /pmc/articles/PMC9582613/ /pubmed/36277219 http://dx.doi.org/10.3389/fphys.2022.909795 Text en Copyright © 2022 Olejniczak, Campbell, Tsai, Tyagarajan, Albrecht and Ripperger. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Olejniczak, Iwona Campbell, Benjamin Tsai, Yuan-Chen Tyagarajan, Shiva K. Albrecht, Urs Ripperger, Jürgen A. Suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice |
title | Suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice |
title_full | Suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice |
title_fullStr | Suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice |
title_full_unstemmed | Suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice |
title_short | Suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice |
title_sort | suprachiasmatic to paraventricular nuclei interaction generates normal food searching rhythms in mice |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582613/ https://www.ncbi.nlm.nih.gov/pubmed/36277219 http://dx.doi.org/10.3389/fphys.2022.909795 |
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