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Sex differences in the traumatic stress response: PTSD symptoms in women recapitulated in female rats
BACKGROUND: Post-traumatic stress disorder (PTSD) affects men and women differently. Not only are women twice as likely as men to develop PTSD, they experience different symptoms and comorbidities associated with PTSD. Yet the dearth of preclinical research on females leaves a notable gap in underst...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034295/ https://www.ncbi.nlm.nih.gov/pubmed/29976248 http://dx.doi.org/10.1186/s13293-018-0191-9 |
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author | Pooley, Apryl E. Benjamin, Rebecca C. Sreedhar, Susheela Eagle, Andrew L. Robison, Alfred J. Mazei-Robison, Michelle S. Breedlove, S. Marc Jordan, Cynthia L. |
author_facet | Pooley, Apryl E. Benjamin, Rebecca C. Sreedhar, Susheela Eagle, Andrew L. Robison, Alfred J. Mazei-Robison, Michelle S. Breedlove, S. Marc Jordan, Cynthia L. |
author_sort | Pooley, Apryl E. |
collection | PubMed |
description | BACKGROUND: Post-traumatic stress disorder (PTSD) affects men and women differently. Not only are women twice as likely as men to develop PTSD, they experience different symptoms and comorbidities associated with PTSD. Yet the dearth of preclinical research on females leaves a notable gap in understanding the underlying neuropathology of this sex difference. METHODS: Using two standard measures of PTSD-like responses in rats, the acoustic startle response (ASR) and dexamethasone suppression test (DST), we tested the effects of traumatic stress in adult male and female rats using two rodent models of PTSD, single prolonged stress and predator exposure. We then examined the neural correlates underlying these responses with cFos and glucocorticoid receptor immunohistochemistry in brain regions implicated in the traumatic stress response. RESULTS: We now report that adult male and female rats across two models of PTSD show consistent sex-specific responses that recapitulate fundamental differences of PTSD in men and women. Trauma-exposed males showed the well-established hyper-responsive phenotype of enhanced ASR and exaggerated negative feedback control of the hypothalamic-pituitary-adrenal axis, while the same traumatic event had little effect on these same measures in females. Dramatic sex differences in how trauma affected cFos and glucocorticoid receptor expression in the brain lend further support to the idea that the trauma response of male and female rats is fundamentally different. CONCLUSIONS: Two standard measures, ASR and DST, might suggest that females are resilient to the effects of traumatic stress, but other measures make it clear that females are not resilient, but simply respond differently to trauma. The next important question to answer is why. We conclude that males and females show fundamentally different responses to trauma that do not simply reflect differences in resilience. The divergent effects of trauma in the brains of males and females begin to shed light on the neurobiological underpinnings of these sex differences, paving the way for improved diagnostics and therapeutics that effectively treat both men and women. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13293-018-0191-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6034295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60342952018-07-12 Sex differences in the traumatic stress response: PTSD symptoms in women recapitulated in female rats Pooley, Apryl E. Benjamin, Rebecca C. Sreedhar, Susheela Eagle, Andrew L. Robison, Alfred J. Mazei-Robison, Michelle S. Breedlove, S. Marc Jordan, Cynthia L. Biol Sex Differ Research BACKGROUND: Post-traumatic stress disorder (PTSD) affects men and women differently. Not only are women twice as likely as men to develop PTSD, they experience different symptoms and comorbidities associated with PTSD. Yet the dearth of preclinical research on females leaves a notable gap in understanding the underlying neuropathology of this sex difference. METHODS: Using two standard measures of PTSD-like responses in rats, the acoustic startle response (ASR) and dexamethasone suppression test (DST), we tested the effects of traumatic stress in adult male and female rats using two rodent models of PTSD, single prolonged stress and predator exposure. We then examined the neural correlates underlying these responses with cFos and glucocorticoid receptor immunohistochemistry in brain regions implicated in the traumatic stress response. RESULTS: We now report that adult male and female rats across two models of PTSD show consistent sex-specific responses that recapitulate fundamental differences of PTSD in men and women. Trauma-exposed males showed the well-established hyper-responsive phenotype of enhanced ASR and exaggerated negative feedback control of the hypothalamic-pituitary-adrenal axis, while the same traumatic event had little effect on these same measures in females. Dramatic sex differences in how trauma affected cFos and glucocorticoid receptor expression in the brain lend further support to the idea that the trauma response of male and female rats is fundamentally different. CONCLUSIONS: Two standard measures, ASR and DST, might suggest that females are resilient to the effects of traumatic stress, but other measures make it clear that females are not resilient, but simply respond differently to trauma. The next important question to answer is why. We conclude that males and females show fundamentally different responses to trauma that do not simply reflect differences in resilience. The divergent effects of trauma in the brains of males and females begin to shed light on the neurobiological underpinnings of these sex differences, paving the way for improved diagnostics and therapeutics that effectively treat both men and women. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13293-018-0191-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-05 /pmc/articles/PMC6034295/ /pubmed/29976248 http://dx.doi.org/10.1186/s13293-018-0191-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Pooley, Apryl E. Benjamin, Rebecca C. Sreedhar, Susheela Eagle, Andrew L. Robison, Alfred J. Mazei-Robison, Michelle S. Breedlove, S. Marc Jordan, Cynthia L. Sex differences in the traumatic stress response: PTSD symptoms in women recapitulated in female rats |
title | Sex differences in the traumatic stress response: PTSD symptoms in women recapitulated in female rats |
title_full | Sex differences in the traumatic stress response: PTSD symptoms in women recapitulated in female rats |
title_fullStr | Sex differences in the traumatic stress response: PTSD symptoms in women recapitulated in female rats |
title_full_unstemmed | Sex differences in the traumatic stress response: PTSD symptoms in women recapitulated in female rats |
title_short | Sex differences in the traumatic stress response: PTSD symptoms in women recapitulated in female rats |
title_sort | sex differences in the traumatic stress response: ptsd symptoms in women recapitulated in female rats |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034295/ https://www.ncbi.nlm.nih.gov/pubmed/29976248 http://dx.doi.org/10.1186/s13293-018-0191-9 |
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