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Hippocampal sharp wave ripples underlie stress susceptibility in male mice
The ventral hippocampus (vHC) is a core brain region for emotional memory. Here, we examined how the vHC regulates stress susceptibility from the level of gene expression to neuronal population dynamics in male mice. Transcriptome analysis of samples from stress-naïve mice revealed that intrinsic ca...
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/PMC10119298/ https://www.ncbi.nlm.nih.gov/pubmed/37080967 http://dx.doi.org/10.1038/s41467-023-37736-x |
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author | Kuga, Nahoko Nakayama, Ryota Morikawa, Shota Yagishita, Haruya Konno, Daichi Shiozaki, Hiromi Honjoya, Natsumi Ikegaya, Yuji Sasaki, Takuya |
author_facet | Kuga, Nahoko Nakayama, Ryota Morikawa, Shota Yagishita, Haruya Konno, Daichi Shiozaki, Hiromi Honjoya, Natsumi Ikegaya, Yuji Sasaki, Takuya |
author_sort | Kuga, Nahoko |
collection | PubMed |
description | The ventral hippocampus (vHC) is a core brain region for emotional memory. Here, we examined how the vHC regulates stress susceptibility from the level of gene expression to neuronal population dynamics in male mice. Transcriptome analysis of samples from stress-naïve mice revealed that intrinsic calbindin (Calb1) expression in the vHC is associated with susceptibility to social defeat stress. Mice with Calb1 gene knockdown in the vHC exhibited increased stress resilience and failed to show the increase in the poststress ventral hippocampal sharp wave ripple (SWR) rate. Poststress vHC SWRs triggered synchronous reactivation of stress memory-encoding neuronal ensembles and facilitated information transfer to the amygdala. Suppression of poststress vHC SWRs by real-time feedback stimulation or walking prevented social behavior deficits. Taken together, our results demonstrate that internal reactivation of memories of negative stressful episodes supported by ventral hippocampal SWRs serves as a crucial neurophysiological substrate for determining stress susceptibility. |
format | Online Article Text |
id | pubmed-10119298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101192982023-04-22 Hippocampal sharp wave ripples underlie stress susceptibility in male mice Kuga, Nahoko Nakayama, Ryota Morikawa, Shota Yagishita, Haruya Konno, Daichi Shiozaki, Hiromi Honjoya, Natsumi Ikegaya, Yuji Sasaki, Takuya Nat Commun Article The ventral hippocampus (vHC) is a core brain region for emotional memory. Here, we examined how the vHC regulates stress susceptibility from the level of gene expression to neuronal population dynamics in male mice. Transcriptome analysis of samples from stress-naïve mice revealed that intrinsic calbindin (Calb1) expression in the vHC is associated with susceptibility to social defeat stress. Mice with Calb1 gene knockdown in the vHC exhibited increased stress resilience and failed to show the increase in the poststress ventral hippocampal sharp wave ripple (SWR) rate. Poststress vHC SWRs triggered synchronous reactivation of stress memory-encoding neuronal ensembles and facilitated information transfer to the amygdala. Suppression of poststress vHC SWRs by real-time feedback stimulation or walking prevented social behavior deficits. Taken together, our results demonstrate that internal reactivation of memories of negative stressful episodes supported by ventral hippocampal SWRs serves as a crucial neurophysiological substrate for determining stress susceptibility. Nature Publishing Group UK 2023-04-20 /pmc/articles/PMC10119298/ /pubmed/37080967 http://dx.doi.org/10.1038/s41467-023-37736-x 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 Kuga, Nahoko Nakayama, Ryota Morikawa, Shota Yagishita, Haruya Konno, Daichi Shiozaki, Hiromi Honjoya, Natsumi Ikegaya, Yuji Sasaki, Takuya Hippocampal sharp wave ripples underlie stress susceptibility in male mice |
title | Hippocampal sharp wave ripples underlie stress susceptibility in male mice |
title_full | Hippocampal sharp wave ripples underlie stress susceptibility in male mice |
title_fullStr | Hippocampal sharp wave ripples underlie stress susceptibility in male mice |
title_full_unstemmed | Hippocampal sharp wave ripples underlie stress susceptibility in male mice |
title_short | Hippocampal sharp wave ripples underlie stress susceptibility in male mice |
title_sort | hippocampal sharp wave ripples underlie stress susceptibility in male mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119298/ https://www.ncbi.nlm.nih.gov/pubmed/37080967 http://dx.doi.org/10.1038/s41467-023-37736-x |
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