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GABAergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression
Rapid eye movement (REM) sleep disturbances are prevalent in various psychiatric disorders. However, the neural circuits that regulate REM sleep remain poorly understood. Here, we found that in male mice, optogenetic activation of rostromedial tegmental nucleus (RMTg) GABAergic neurons immediately c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729601/ https://www.ncbi.nlm.nih.gov/pubmed/36477665 http://dx.doi.org/10.1038/s41467-022-35299-x |
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author | Zhao, Ya-Nan Jiang, Jian-Bo Tao, Shi-Yuan Zhang, Yang Chen, Ze-Ka Qu, Wei-Min Huang, Zhi-Li Yang, Su-Rong |
author_facet | Zhao, Ya-Nan Jiang, Jian-Bo Tao, Shi-Yuan Zhang, Yang Chen, Ze-Ka Qu, Wei-Min Huang, Zhi-Li Yang, Su-Rong |
author_sort | Zhao, Ya-Nan |
collection | PubMed |
description | Rapid eye movement (REM) sleep disturbances are prevalent in various psychiatric disorders. However, the neural circuits that regulate REM sleep remain poorly understood. Here, we found that in male mice, optogenetic activation of rostromedial tegmental nucleus (RMTg) GABAergic neurons immediately converted REM sleep to arousal and then initiated non-REM (NREM) sleep. Conversely, laser-mediated inactivation completely converted NREM to REM sleep and prolonged REM sleep duration. The activity of RMTg GABAergic neurons increased to a high discharge level at the termination of REM sleep. RMTg GABAergic neurons directly converted REM sleep to wakefulness and NREM sleep via inhibitory projections to the laterodorsal tegmentum (LDT) and lateral hypothalamus (LH), respectively. Furthermore, LDT glutamatergic neurons were responsible for the REM sleep-wake transitions following photostimulation of the RMTg(GABA)-LDT circuit. Thus, RMTg GABAergic neurons are essential for suppressing the induction and maintenance of REM sleep. |
format | Online Article Text |
id | pubmed-9729601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97296012022-12-09 GABAergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression Zhao, Ya-Nan Jiang, Jian-Bo Tao, Shi-Yuan Zhang, Yang Chen, Ze-Ka Qu, Wei-Min Huang, Zhi-Li Yang, Su-Rong Nat Commun Article Rapid eye movement (REM) sleep disturbances are prevalent in various psychiatric disorders. However, the neural circuits that regulate REM sleep remain poorly understood. Here, we found that in male mice, optogenetic activation of rostromedial tegmental nucleus (RMTg) GABAergic neurons immediately converted REM sleep to arousal and then initiated non-REM (NREM) sleep. Conversely, laser-mediated inactivation completely converted NREM to REM sleep and prolonged REM sleep duration. The activity of RMTg GABAergic neurons increased to a high discharge level at the termination of REM sleep. RMTg GABAergic neurons directly converted REM sleep to wakefulness and NREM sleep via inhibitory projections to the laterodorsal tegmentum (LDT) and lateral hypothalamus (LH), respectively. Furthermore, LDT glutamatergic neurons were responsible for the REM sleep-wake transitions following photostimulation of the RMTg(GABA)-LDT circuit. Thus, RMTg GABAergic neurons are essential for suppressing the induction and maintenance of REM sleep. Nature Publishing Group UK 2022-12-07 /pmc/articles/PMC9729601/ /pubmed/36477665 http://dx.doi.org/10.1038/s41467-022-35299-x Text en © The Author(s) 2022 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 Zhao, Ya-Nan Jiang, Jian-Bo Tao, Shi-Yuan Zhang, Yang Chen, Ze-Ka Qu, Wei-Min Huang, Zhi-Li Yang, Su-Rong GABAergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression |
title | GABAergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression |
title_full | GABAergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression |
title_fullStr | GABAergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression |
title_full_unstemmed | GABAergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression |
title_short | GABAergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression |
title_sort | gabaergic neurons in the rostromedial tegmental nucleus are essential for rapid eye movement sleep suppression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729601/ https://www.ncbi.nlm.nih.gov/pubmed/36477665 http://dx.doi.org/10.1038/s41467-022-35299-x |
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