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Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice
The parasubthalamic nucleus (PSTN) is considered to be involved in motivation, feeding and hunting, all of which are highly depending on wakefulness. However, the roles and underlying neural circuits of the PSTN in wakefulness remain unclear. Neurons expressing calretinin (CR) account for the majori...
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/PMC10126000/ https://www.ncbi.nlm.nih.gov/pubmed/37095092 http://dx.doi.org/10.1038/s41467-023-37797-y |
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author | Guo, Han Jiang, Jian-Bo Xu, Wei Zhang, Mu-Tian Chen, Hui Shi, Huan-Ying Wang, Lu He, Miao Lazarus, Michael Li, Shan-Qun Huang, Zhi-Li Qu, Wei-Min |
author_facet | Guo, Han Jiang, Jian-Bo Xu, Wei Zhang, Mu-Tian Chen, Hui Shi, Huan-Ying Wang, Lu He, Miao Lazarus, Michael Li, Shan-Qun Huang, Zhi-Li Qu, Wei-Min |
author_sort | Guo, Han |
collection | PubMed |
description | The parasubthalamic nucleus (PSTN) is considered to be involved in motivation, feeding and hunting, all of which are highly depending on wakefulness. However, the roles and underlying neural circuits of the PSTN in wakefulness remain unclear. Neurons expressing calretinin (CR) account for the majority of PSTN neurons. In this study in male mice, fiber photometry recordings showed that the activity of PSTN(CR) neurons increased at the transitions from non-rapid eye movement (non-REM, NREM) sleep to either wakefulness or REM sleep, as well as exploratory behavior. Chemogenetic and optogenetic experiments demonstrated that PSTN(CR) neurons were necessary for initiating and/or maintaining arousal associated with exploration. Photoactivation of projections of PSTN(CR) neurons revealed that they regulated exploration-related wakefulness by innervating the ventral tegmental area. Collectively, our findings indicate that PSTN(CR) circuitry is essential for the induction and maintenance of the awake state associated with exploration. |
format | Online Article Text |
id | pubmed-10126000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101260002023-04-26 Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice Guo, Han Jiang, Jian-Bo Xu, Wei Zhang, Mu-Tian Chen, Hui Shi, Huan-Ying Wang, Lu He, Miao Lazarus, Michael Li, Shan-Qun Huang, Zhi-Li Qu, Wei-Min Nat Commun Article The parasubthalamic nucleus (PSTN) is considered to be involved in motivation, feeding and hunting, all of which are highly depending on wakefulness. However, the roles and underlying neural circuits of the PSTN in wakefulness remain unclear. Neurons expressing calretinin (CR) account for the majority of PSTN neurons. In this study in male mice, fiber photometry recordings showed that the activity of PSTN(CR) neurons increased at the transitions from non-rapid eye movement (non-REM, NREM) sleep to either wakefulness or REM sleep, as well as exploratory behavior. Chemogenetic and optogenetic experiments demonstrated that PSTN(CR) neurons were necessary for initiating and/or maintaining arousal associated with exploration. Photoactivation of projections of PSTN(CR) neurons revealed that they regulated exploration-related wakefulness by innervating the ventral tegmental area. Collectively, our findings indicate that PSTN(CR) circuitry is essential for the induction and maintenance of the awake state associated with exploration. Nature Publishing Group UK 2023-04-24 /pmc/articles/PMC10126000/ /pubmed/37095092 http://dx.doi.org/10.1038/s41467-023-37797-y 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Guo, Han Jiang, Jian-Bo Xu, Wei Zhang, Mu-Tian Chen, Hui Shi, Huan-Ying Wang, Lu He, Miao Lazarus, Michael Li, Shan-Qun Huang, Zhi-Li Qu, Wei-Min Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice |
title | Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice |
title_full | Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice |
title_fullStr | Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice |
title_full_unstemmed | Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice |
title_short | Parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice |
title_sort | parasubthalamic calretinin neurons modulate wakefulness associated with exploration in male mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126000/ https://www.ncbi.nlm.nih.gov/pubmed/37095092 http://dx.doi.org/10.1038/s41467-023-37797-y |
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