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Common and differential transcriptional responses to different models of traumatic stress exposure in rats

The effect of six different traumatic stress protocols on the transcriptome of the rat adrenal gland was examined using RNA sequencing. These protocols included chronic variable stress, chronic shock, social defeat and social isolation. The response of the transcriptome to stress suggested that ther...

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Autores principales: Jacobson, Moriah L., Kim, Lydia A., Patro, Robert, Rosati, Barbara, McKinnon, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107654/
https://www.ncbi.nlm.nih.gov/pubmed/30139969
http://dx.doi.org/10.1038/s41398-018-0223-6
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author Jacobson, Moriah L.
Kim, Lydia A.
Patro, Robert
Rosati, Barbara
McKinnon, David
author_facet Jacobson, Moriah L.
Kim, Lydia A.
Patro, Robert
Rosati, Barbara
McKinnon, David
author_sort Jacobson, Moriah L.
collection PubMed
description The effect of six different traumatic stress protocols on the transcriptome of the rat adrenal gland was examined using RNA sequencing. These protocols included chronic variable stress, chronic shock, social defeat and social isolation. The response of the transcriptome to stress suggested that there are genes that respond in a universal or stress modality-independent manner, as well as genes that respond in a stress modality-specific manner. Using a small number of the genes selected from the modality-independent set of stress-sensitive genes, a sensitive and robust measure of chronic stress exposure was developed. This stress-sensitive gene expression (SSGE) index could detect chronic traumatic stress exposure in a wide range of different stress models in a manner that was relatively independent of the modality of stress exposure and that paralleled the intensity of stress exposure in a dose-dependent manner. This measure could reliably distinguish control and stressed individuals in the case of animals exposed to the most intense stress protocols. The response of a subset of the modality-specific genes could also distinguish some types of stress exposure, based solely on changes in the pattern of gene expression. The results suggest that it is possible to develop diagnostic measures of traumatic stress exposure based solely on changes in the level of expression of a relatively small number of genes.
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spelling pubmed-61076542018-08-27 Common and differential transcriptional responses to different models of traumatic stress exposure in rats Jacobson, Moriah L. Kim, Lydia A. Patro, Robert Rosati, Barbara McKinnon, David Transl Psychiatry Article The effect of six different traumatic stress protocols on the transcriptome of the rat adrenal gland was examined using RNA sequencing. These protocols included chronic variable stress, chronic shock, social defeat and social isolation. The response of the transcriptome to stress suggested that there are genes that respond in a universal or stress modality-independent manner, as well as genes that respond in a stress modality-specific manner. Using a small number of the genes selected from the modality-independent set of stress-sensitive genes, a sensitive and robust measure of chronic stress exposure was developed. This stress-sensitive gene expression (SSGE) index could detect chronic traumatic stress exposure in a wide range of different stress models in a manner that was relatively independent of the modality of stress exposure and that paralleled the intensity of stress exposure in a dose-dependent manner. This measure could reliably distinguish control and stressed individuals in the case of animals exposed to the most intense stress protocols. The response of a subset of the modality-specific genes could also distinguish some types of stress exposure, based solely on changes in the pattern of gene expression. The results suggest that it is possible to develop diagnostic measures of traumatic stress exposure based solely on changes in the level of expression of a relatively small number of genes. Nature Publishing Group UK 2018-08-23 /pmc/articles/PMC6107654/ /pubmed/30139969 http://dx.doi.org/10.1038/s41398-018-0223-6 Text en © The Author(s) 2018 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
Jacobson, Moriah L.
Kim, Lydia A.
Patro, Robert
Rosati, Barbara
McKinnon, David
Common and differential transcriptional responses to different models of traumatic stress exposure in rats
title Common and differential transcriptional responses to different models of traumatic stress exposure in rats
title_full Common and differential transcriptional responses to different models of traumatic stress exposure in rats
title_fullStr Common and differential transcriptional responses to different models of traumatic stress exposure in rats
title_full_unstemmed Common and differential transcriptional responses to different models of traumatic stress exposure in rats
title_short Common and differential transcriptional responses to different models of traumatic stress exposure in rats
title_sort common and differential transcriptional responses to different models of traumatic stress exposure in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107654/
https://www.ncbi.nlm.nih.gov/pubmed/30139969
http://dx.doi.org/10.1038/s41398-018-0223-6
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