Cargando…

Neuronal substrates underlying stress resilience and susceptibility in rats

BACKGROUND: Stress and stressful life events have repeatedly been shown as causally related to depression. The Chronic Mild Stress rat model is a valid model of stress-induced depression. Like humans, rats display great heterogeneity in their response to stress and adversity. Hence some individuals...

Descripción completa

Detalles Bibliográficos
Autores principales: Febbraro, Fabia, Svenningsen, Katrine, Tran, Thao Phuong, Wiborg, Ove
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473563/
https://www.ncbi.nlm.nih.gov/pubmed/28622391
http://dx.doi.org/10.1371/journal.pone.0179434
_version_ 1783244309656502272
author Febbraro, Fabia
Svenningsen, Katrine
Tran, Thao Phuong
Wiborg, Ove
author_facet Febbraro, Fabia
Svenningsen, Katrine
Tran, Thao Phuong
Wiborg, Ove
author_sort Febbraro, Fabia
collection PubMed
description BACKGROUND: Stress and stressful life events have repeatedly been shown as causally related to depression. The Chronic Mild Stress rat model is a valid model of stress-induced depression. Like humans, rats display great heterogeneity in their response to stress and adversity. Hence some individuals are stress-sensitive and prone to develop depression-like behaviour in response to modest stressors, while others are stress-resilient and remain essentially symptom free. OBJECTIVES: Compared to the large body of research, which describes stress-induced maladaptive neurobiological changes, relatively little attention has been devoted to understand resiliency to stress. The aim of the present study was to identify changes in neuronal activity, associated with stress-resilient and stress-susceptible chronic mild stress endophenotypes, by examining c-Fos expression in 13 different brain areas. Changes in c-Fos expression have been reported as associated to stressful conditions. METHODS: Stress-induced modulation of neuronal activation patterns in response to the chronic mild stress paradigm was mapped using the immediate early gene expression c-Fos as a marker. Quantification of the c-Fos-like immunoreactivity responses was done by semi-automated profile counting procedures and design-based stereology. RESULTS: Exposure to chronic mild stress significantly altered c-Fos expression in a total of 6 out of 13 investigated areas. Chronic mild stress was found to suppress the c-Fos response within the magnocellular ventral lateral geniculate nucleus of both stress subgroups. In the the lateral and ventral orbital cortices of stress-resilient rats, the c-Fos like immunoreactivity response was also repressed by stress exposure. On the contrary the c-Fos response within the amygdala, medial habenula, and infralimbic cortex was increased selectively for the stress-susceptible rats. CONCLUSIONS: The study was initiated to characterize neuronal substrates associated with stress-coping mechanisms. Six areas, all of which represents limbic structures, were found to be sensitive to stress exposure. The effects within these areas associate to the hedonic status of the rats. Hence, these areas might be associated to stress-coping mechanisms underlying the chronic mild stress induced segregation into stress-susceptible and stress-resilient endophenotypes.
format Online
Article
Text
id pubmed-5473563
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-54735632017-06-22 Neuronal substrates underlying stress resilience and susceptibility in rats Febbraro, Fabia Svenningsen, Katrine Tran, Thao Phuong Wiborg, Ove PLoS One Research Article BACKGROUND: Stress and stressful life events have repeatedly been shown as causally related to depression. The Chronic Mild Stress rat model is a valid model of stress-induced depression. Like humans, rats display great heterogeneity in their response to stress and adversity. Hence some individuals are stress-sensitive and prone to develop depression-like behaviour in response to modest stressors, while others are stress-resilient and remain essentially symptom free. OBJECTIVES: Compared to the large body of research, which describes stress-induced maladaptive neurobiological changes, relatively little attention has been devoted to understand resiliency to stress. The aim of the present study was to identify changes in neuronal activity, associated with stress-resilient and stress-susceptible chronic mild stress endophenotypes, by examining c-Fos expression in 13 different brain areas. Changes in c-Fos expression have been reported as associated to stressful conditions. METHODS: Stress-induced modulation of neuronal activation patterns in response to the chronic mild stress paradigm was mapped using the immediate early gene expression c-Fos as a marker. Quantification of the c-Fos-like immunoreactivity responses was done by semi-automated profile counting procedures and design-based stereology. RESULTS: Exposure to chronic mild stress significantly altered c-Fos expression in a total of 6 out of 13 investigated areas. Chronic mild stress was found to suppress the c-Fos response within the magnocellular ventral lateral geniculate nucleus of both stress subgroups. In the the lateral and ventral orbital cortices of stress-resilient rats, the c-Fos like immunoreactivity response was also repressed by stress exposure. On the contrary the c-Fos response within the amygdala, medial habenula, and infralimbic cortex was increased selectively for the stress-susceptible rats. CONCLUSIONS: The study was initiated to characterize neuronal substrates associated with stress-coping mechanisms. Six areas, all of which represents limbic structures, were found to be sensitive to stress exposure. The effects within these areas associate to the hedonic status of the rats. Hence, these areas might be associated to stress-coping mechanisms underlying the chronic mild stress induced segregation into stress-susceptible and stress-resilient endophenotypes. Public Library of Science 2017-06-16 /pmc/articles/PMC5473563/ /pubmed/28622391 http://dx.doi.org/10.1371/journal.pone.0179434 Text en © 2017 Febbraro et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Febbraro, Fabia
Svenningsen, Katrine
Tran, Thao Phuong
Wiborg, Ove
Neuronal substrates underlying stress resilience and susceptibility in rats
title Neuronal substrates underlying stress resilience and susceptibility in rats
title_full Neuronal substrates underlying stress resilience and susceptibility in rats
title_fullStr Neuronal substrates underlying stress resilience and susceptibility in rats
title_full_unstemmed Neuronal substrates underlying stress resilience and susceptibility in rats
title_short Neuronal substrates underlying stress resilience and susceptibility in rats
title_sort neuronal substrates underlying stress resilience and susceptibility in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473563/
https://www.ncbi.nlm.nih.gov/pubmed/28622391
http://dx.doi.org/10.1371/journal.pone.0179434
work_keys_str_mv AT febbrarofabia neuronalsubstratesunderlyingstressresilienceandsusceptibilityinrats
AT svenningsenkatrine neuronalsubstratesunderlyingstressresilienceandsusceptibilityinrats
AT tranthaophuong neuronalsubstratesunderlyingstressresilienceandsusceptibilityinrats
AT wiborgove neuronalsubstratesunderlyingstressresilienceandsusceptibilityinrats