Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kuga, Nahoko, Nakayama, Ryota, Morikawa, Shota, Yagishita, Haruya, Konno, Daichi, Shiozaki, Hiromi, Honjoya, Natsumi, Ikegaya, Yuji, Sasaki, Takuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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
_version_ 1785028995288399872
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
work_keys_str_mv AT kuganahoko hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice
AT nakayamaryota hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice
AT morikawashota hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice
AT yagishitaharuya hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice
AT konnodaichi hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice
AT shiozakihiromi hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice
AT honjoyanatsumi hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice
AT ikegayayuji hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice
AT sasakitakuya hippocampalsharpwaveripplesunderliestresssusceptibilityinmalemice