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Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study

Psychosocial stress is a risk factor for the development of depression. Recent evidence suggests that glial activation could contribute to the development of depressive-like behaviour. This study aimed to evaluate in vivo whether repeated social defeat (RSD) induces short- and long-term inflammatory...

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Autores principales: Kopschina Feltes, Paula, de Vries, Erik FJ, Juarez-Orozco, Luis E, Kurtys, Ewelina, Dierckx, Rudi AJO, Moriguchi-Jeckel, Cristina M, Doorduin, Janine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399731/
https://www.ncbi.nlm.nih.gov/pubmed/29271288
http://dx.doi.org/10.1177/0271678X17747189
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author Kopschina Feltes, Paula
de Vries, Erik FJ
Juarez-Orozco, Luis E
Kurtys, Ewelina
Dierckx, Rudi AJO
Moriguchi-Jeckel, Cristina M
Doorduin, Janine
author_facet Kopschina Feltes, Paula
de Vries, Erik FJ
Juarez-Orozco, Luis E
Kurtys, Ewelina
Dierckx, Rudi AJO
Moriguchi-Jeckel, Cristina M
Doorduin, Janine
author_sort Kopschina Feltes, Paula
collection PubMed
description Psychosocial stress is a risk factor for the development of depression. Recent evidence suggests that glial activation could contribute to the development of depressive-like behaviour. This study aimed to evaluate in vivo whether repeated social defeat (RSD) induces short- and long-term inflammatory and metabolic alterations in the brain through positron emission tomography (PET). Male Wistar rats (n = 40) were exposed to RSD by dominant Long-Evans rats on five consecutive days. Behavioural and biochemical alterations were assessed at baseline, day 5/6 and day 24/25 after the RSD protocol. Glial activation ((11)C-PK11195 PET) and changes in brain metabolism ((18)F-FDG PET) were evaluated on day 6, 11 and 25 (short-term), and at 3 and 6 months (long-term). Defeated rats showed transient depressive- and anxiety-like behaviour, increased corticosterone and brain IL-1β levels, as well as glial activation and brain hypometabolism in the first month after RSD. During the third- and six-month follow-up, no between-group differences in any investigated parameter were found. Therefore, non-invasive PET imaging demonstrated that RSD induces transient glial activation and reduces brain glucose metabolism in rats. These imaging findings were associated with stress-induced behavioural changes and support the hypothesis that neuroinflammation could be a contributing factor in the development of depression.
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spelling pubmed-63997312019-03-16 Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study Kopschina Feltes, Paula de Vries, Erik FJ Juarez-Orozco, Luis E Kurtys, Ewelina Dierckx, Rudi AJO Moriguchi-Jeckel, Cristina M Doorduin, Janine J Cereb Blood Flow Metab Original Articles Psychosocial stress is a risk factor for the development of depression. Recent evidence suggests that glial activation could contribute to the development of depressive-like behaviour. This study aimed to evaluate in vivo whether repeated social defeat (RSD) induces short- and long-term inflammatory and metabolic alterations in the brain through positron emission tomography (PET). Male Wistar rats (n = 40) were exposed to RSD by dominant Long-Evans rats on five consecutive days. Behavioural and biochemical alterations were assessed at baseline, day 5/6 and day 24/25 after the RSD protocol. Glial activation ((11)C-PK11195 PET) and changes in brain metabolism ((18)F-FDG PET) were evaluated on day 6, 11 and 25 (short-term), and at 3 and 6 months (long-term). Defeated rats showed transient depressive- and anxiety-like behaviour, increased corticosterone and brain IL-1β levels, as well as glial activation and brain hypometabolism in the first month after RSD. During the third- and six-month follow-up, no between-group differences in any investigated parameter were found. Therefore, non-invasive PET imaging demonstrated that RSD induces transient glial activation and reduces brain glucose metabolism in rats. These imaging findings were associated with stress-induced behavioural changes and support the hypothesis that neuroinflammation could be a contributing factor in the development of depression. SAGE Publications 2017-12-22 2019-03 /pmc/articles/PMC6399731/ /pubmed/29271288 http://dx.doi.org/10.1177/0271678X17747189 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Kopschina Feltes, Paula
de Vries, Erik FJ
Juarez-Orozco, Luis E
Kurtys, Ewelina
Dierckx, Rudi AJO
Moriguchi-Jeckel, Cristina M
Doorduin, Janine
Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study
title Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study
title_full Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study
title_fullStr Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study
title_full_unstemmed Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study
title_short Repeated social defeat induces transient glial activation and brain hypometabolism: A positron emission tomography imaging study
title_sort repeated social defeat induces transient glial activation and brain hypometabolism: a positron emission tomography imaging study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399731/
https://www.ncbi.nlm.nih.gov/pubmed/29271288
http://dx.doi.org/10.1177/0271678X17747189
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