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Social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex
The ventromedial prefrontal cortex (vmPFC) plays key roles in higher cognitive abilities, including mental representations and the regulation of emotion. Previous studies have reported that vmPFC activity is altered in depressed human patients, highlighting this subregion as a major site of dysfunct...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603183/ https://www.ncbi.nlm.nih.gov/pubmed/31263153 http://dx.doi.org/10.1038/s41598-019-45833-5 |
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author | Abe, Reimi Okada, Sakura Nakayama, Ryota Ikegaya, Yuji Sasaki, Takuya |
author_facet | Abe, Reimi Okada, Sakura Nakayama, Ryota Ikegaya, Yuji Sasaki, Takuya |
author_sort | Abe, Reimi |
collection | PubMed |
description | The ventromedial prefrontal cortex (vmPFC) plays key roles in higher cognitive abilities, including mental representations and the regulation of emotion. Previous studies have reported that vmPFC activity is altered in depressed human patients, highlighting this subregion as a major site of dysfunction in neuropsychiatric diseases. To examine how neuronal activity at spike levels in the vmPFC is altered by social defeat stress, we performed electrophysiological multiunit recordings along the dorsoventral axis of the mPFC of freely moving mice. Chronic social defeat stress-susceptible mice showing an impairment in social interaction exhibited significant reductions in the overall spike frequencies of neurons in the vmPFC, but not in the dorsal mPFC. Analysis of local field potentials revealed that the vmPFC generated spatially constrained 20–40 Hz events lasting hundreds of milliseconds, with an average event frequency of 0.05 Hz; during these events, a subset of neurons were transiently inhibited. The frequency of 20–40 Hz events in the vmPFC was reduced in defeated stress-susceptible animals, and this decrease was reversed by systemic ketamine administration. The novel neurophysiological correlates of stress-induced changes in the vmPFC advance the understanding of the neural basis of stress-induced dysregulation of social behavior. |
format | Online Article Text |
id | pubmed-6603183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66031832019-07-14 Social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex Abe, Reimi Okada, Sakura Nakayama, Ryota Ikegaya, Yuji Sasaki, Takuya Sci Rep Article The ventromedial prefrontal cortex (vmPFC) plays key roles in higher cognitive abilities, including mental representations and the regulation of emotion. Previous studies have reported that vmPFC activity is altered in depressed human patients, highlighting this subregion as a major site of dysfunction in neuropsychiatric diseases. To examine how neuronal activity at spike levels in the vmPFC is altered by social defeat stress, we performed electrophysiological multiunit recordings along the dorsoventral axis of the mPFC of freely moving mice. Chronic social defeat stress-susceptible mice showing an impairment in social interaction exhibited significant reductions in the overall spike frequencies of neurons in the vmPFC, but not in the dorsal mPFC. Analysis of local field potentials revealed that the vmPFC generated spatially constrained 20–40 Hz events lasting hundreds of milliseconds, with an average event frequency of 0.05 Hz; during these events, a subset of neurons were transiently inhibited. The frequency of 20–40 Hz events in the vmPFC was reduced in defeated stress-susceptible animals, and this decrease was reversed by systemic ketamine administration. The novel neurophysiological correlates of stress-induced changes in the vmPFC advance the understanding of the neural basis of stress-induced dysregulation of social behavior. Nature Publishing Group UK 2019-07-01 /pmc/articles/PMC6603183/ /pubmed/31263153 http://dx.doi.org/10.1038/s41598-019-45833-5 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Abe, Reimi Okada, Sakura Nakayama, Ryota Ikegaya, Yuji Sasaki, Takuya Social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex |
title | Social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex |
title_full | Social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex |
title_fullStr | Social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex |
title_full_unstemmed | Social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex |
title_short | Social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex |
title_sort | social defeat stress causes selective attenuation of neuronal activity in the ventromedial prefrontal cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603183/ https://www.ncbi.nlm.nih.gov/pubmed/31263153 http://dx.doi.org/10.1038/s41598-019-45833-5 |
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