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Subcortical serotonin 5HT(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice
Binge alcohol consumption induces discrete social and arousal disturbances in human populations that promote increased drinking and accelerate the progression of Alcohol Use Disorder. Here, we show in a mouse model that binge alcohol consumption disrupts social recognition in females and potentiates...
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/PMC10066391/ https://www.ncbi.nlm.nih.gov/pubmed/37002196 http://dx.doi.org/10.1038/s41467-023-36808-2 |
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author | Flanigan, M. E. Hon, O. J. D’Ambrosio, S. Boyt, K. M. Hassanein, L. Castle, M. Haun, H. L. Pina, M. M. Kash, T. L. |
author_facet | Flanigan, M. E. Hon, O. J. D’Ambrosio, S. Boyt, K. M. Hassanein, L. Castle, M. Haun, H. L. Pina, M. M. Kash, T. L. |
author_sort | Flanigan, M. E. |
collection | PubMed |
description | Binge alcohol consumption induces discrete social and arousal disturbances in human populations that promote increased drinking and accelerate the progression of Alcohol Use Disorder. Here, we show in a mouse model that binge alcohol consumption disrupts social recognition in females and potentiates sensorimotor arousal in males. These negative behavioral outcomes were associated with sex-specific adaptations in serotonergic signaling systems within the lateral habenula (LHb) and the bed nucleus of the stria terminalis (BNST), particularly those related to the receptor 5HT(2c). While both BNST and LHb neurons expressing this receptor display potentiated activation following binge alcohol consumption, the primary causal mechanism underlying the effects of alcohol on social and arousal behaviors appears to be excessive activation of LHb(5HT2c) neurons. These findings may have valuable implications for the development of sex-specific treatments for mood and alcohol use disorders targeting the brain’s serotonin system. |
format | Online Article Text |
id | pubmed-10066391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100663912023-04-02 Subcortical serotonin 5HT(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice Flanigan, M. E. Hon, O. J. D’Ambrosio, S. Boyt, K. M. Hassanein, L. Castle, M. Haun, H. L. Pina, M. M. Kash, T. L. Nat Commun Article Binge alcohol consumption induces discrete social and arousal disturbances in human populations that promote increased drinking and accelerate the progression of Alcohol Use Disorder. Here, we show in a mouse model that binge alcohol consumption disrupts social recognition in females and potentiates sensorimotor arousal in males. These negative behavioral outcomes were associated with sex-specific adaptations in serotonergic signaling systems within the lateral habenula (LHb) and the bed nucleus of the stria terminalis (BNST), particularly those related to the receptor 5HT(2c). While both BNST and LHb neurons expressing this receptor display potentiated activation following binge alcohol consumption, the primary causal mechanism underlying the effects of alcohol on social and arousal behaviors appears to be excessive activation of LHb(5HT2c) neurons. These findings may have valuable implications for the development of sex-specific treatments for mood and alcohol use disorders targeting the brain’s serotonin system. Nature Publishing Group UK 2023-03-31 /pmc/articles/PMC10066391/ /pubmed/37002196 http://dx.doi.org/10.1038/s41467-023-36808-2 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 Flanigan, M. E. Hon, O. J. D’Ambrosio, S. Boyt, K. M. Hassanein, L. Castle, M. Haun, H. L. Pina, M. M. Kash, T. L. Subcortical serotonin 5HT(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice |
title | Subcortical serotonin 5HT(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice |
title_full | Subcortical serotonin 5HT(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice |
title_fullStr | Subcortical serotonin 5HT(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice |
title_full_unstemmed | Subcortical serotonin 5HT(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice |
title_short | Subcortical serotonin 5HT(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice |
title_sort | subcortical serotonin 5ht(2c) receptor-containing neurons sex-specifically regulate binge-like alcohol consumption, social, and arousal behaviors in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066391/ https://www.ncbi.nlm.nih.gov/pubmed/37002196 http://dx.doi.org/10.1038/s41467-023-36808-2 |
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