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Early-life stress and inflammation: A systematic review of a key experimental approach in rodents
Repeated maternal separation is the most widely used pre-clinical approach to investigate the relationship between early-life chronic stress and its neuropsychiatric and physical consequences. In this systematic review, we identified 46 studies that conducted repeated maternal separation or single-e...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780197/ https://www.ncbi.nlm.nih.gov/pubmed/33447663 http://dx.doi.org/10.1177/2398212820978049 |
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author | Dutcher, Ethan G. Pama, E.A. Claudia Lynall, Mary-Ellen Khan, Shahid Clatworthy, Menna R. Robbins, Trevor W. Bullmore, Edward T. Dalley, Jeffrey W. |
author_facet | Dutcher, Ethan G. Pama, E.A. Claudia Lynall, Mary-Ellen Khan, Shahid Clatworthy, Menna R. Robbins, Trevor W. Bullmore, Edward T. Dalley, Jeffrey W. |
author_sort | Dutcher, Ethan G. |
collection | PubMed |
description | Repeated maternal separation is the most widely used pre-clinical approach to investigate the relationship between early-life chronic stress and its neuropsychiatric and physical consequences. In this systematic review, we identified 46 studies that conducted repeated maternal separation or single-episode maternal separation and reported measurements of interleukin-1b, interleukin-6, interleukin-10, tumour necrosis factor-alpha, or microglia activation and density. We report that in the short-term and in the context of later-life stress, repeated maternal separation has pro-inflammatory immune consequences in diverse tissues. Repeated maternal separation animals exhibit greater microglial activation and elevated pro-inflammatory cytokine signalling in key brain regions implicated in human psychiatric disorders. Notably, repeated maternal separation generally has no long-term effect on cytokine expression in any tissue in the absence of later-life stress. These observations suggest that the elevated inflammatory signalling that has been reported in humans with a history of early-life stress may be the joint consequence of ongoing stressor exposure together with potentiated neural and/or immune responsiveness to stressors. Finally, our findings provide detailed guidance for future studies interrogating the causal roles of early-life stress and inflammation in disorders such as major depression. |
format | Online Article Text |
id | pubmed-7780197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-77801972021-01-13 Early-life stress and inflammation: A systematic review of a key experimental approach in rodents Dutcher, Ethan G. Pama, E.A. Claudia Lynall, Mary-Ellen Khan, Shahid Clatworthy, Menna R. Robbins, Trevor W. Bullmore, Edward T. Dalley, Jeffrey W. Brain Neurosci Adv Review Article Repeated maternal separation is the most widely used pre-clinical approach to investigate the relationship between early-life chronic stress and its neuropsychiatric and physical consequences. In this systematic review, we identified 46 studies that conducted repeated maternal separation or single-episode maternal separation and reported measurements of interleukin-1b, interleukin-6, interleukin-10, tumour necrosis factor-alpha, or microglia activation and density. We report that in the short-term and in the context of later-life stress, repeated maternal separation has pro-inflammatory immune consequences in diverse tissues. Repeated maternal separation animals exhibit greater microglial activation and elevated pro-inflammatory cytokine signalling in key brain regions implicated in human psychiatric disorders. Notably, repeated maternal separation generally has no long-term effect on cytokine expression in any tissue in the absence of later-life stress. These observations suggest that the elevated inflammatory signalling that has been reported in humans with a history of early-life stress may be the joint consequence of ongoing stressor exposure together with potentiated neural and/or immune responsiveness to stressors. Finally, our findings provide detailed guidance for future studies interrogating the causal roles of early-life stress and inflammation in disorders such as major depression. SAGE Publications 2020-12-28 /pmc/articles/PMC7780197/ /pubmed/33447663 http://dx.doi.org/10.1177/2398212820978049 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Article Dutcher, Ethan G. Pama, E.A. Claudia Lynall, Mary-Ellen Khan, Shahid Clatworthy, Menna R. Robbins, Trevor W. Bullmore, Edward T. Dalley, Jeffrey W. Early-life stress and inflammation: A systematic review of a key experimental approach in rodents |
title | Early-life stress and inflammation: A systematic review of a key experimental approach in rodents |
title_full | Early-life stress and inflammation: A systematic review of a key experimental approach in rodents |
title_fullStr | Early-life stress and inflammation: A systematic review of a key experimental approach in rodents |
title_full_unstemmed | Early-life stress and inflammation: A systematic review of a key experimental approach in rodents |
title_short | Early-life stress and inflammation: A systematic review of a key experimental approach in rodents |
title_sort | early-life stress and inflammation: a systematic review of a key experimental approach in rodents |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780197/ https://www.ncbi.nlm.nih.gov/pubmed/33447663 http://dx.doi.org/10.1177/2398212820978049 |
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