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Fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder
Although selective serotonin reuptake inhibitors (SSRIs) are first-line treatment for post-traumatic stress disorder (PTSD) patients, their therapeutic efficacy is limited. Childhood adversities are considered a risk factor for developing PTSD in adulthood but may trigger PTSD without additional tra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802710/ https://www.ncbi.nlm.nih.gov/pubmed/29187754 http://dx.doi.org/10.1038/s41398-017-0014-5 |
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author | Ariel, Lior Inbar, Sapir Edut, Schachaf Richter-Levin, Gal |
author_facet | Ariel, Lior Inbar, Sapir Edut, Schachaf Richter-Levin, Gal |
author_sort | Ariel, Lior |
collection | PubMed |
description | Although selective serotonin reuptake inhibitors (SSRIs) are first-line treatment for post-traumatic stress disorder (PTSD) patients, their therapeutic efficacy is limited. Childhood adversities are considered a risk factor for developing PTSD in adulthood but may trigger PTSD without additional trauma in some individuals. Nevertheless, just as childhood is considered a vulnerable period it may also be an effective period for preventive treatment. Using a rat model of childhood-induced PTSD, pre-pubertal stress (juvenile stress, JVS), we compared the therapeutic effects of fluoxetine and examined the effectiveness of 1 month of fluoxetine treatment following JVS and into adulthood compared to treatment in adulthood. Since not all individuals develop PTSD following a trauma, comparing only group means is not the adequate type of analysis. We employed a behavioral profiling approach, which analyzes individual differences compared to the normal behavior of a control group. Animals exposed to JVS exhibited a higher proportion of affected animals as measured using the elevated plus maze 8 weeks after JVS. Fluoxetine treatment following the JVS significantly decreased the proportion of affected animals as measured in adulthood. Fluoxetine treatment in adulthood was not effective. The results support the notion that childhood is not only a vulnerable period but also an effective period for preventive treatment. |
format | Online Article Text |
id | pubmed-5802710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58027102018-02-08 Fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder Ariel, Lior Inbar, Sapir Edut, Schachaf Richter-Levin, Gal Transl Psychiatry Article Although selective serotonin reuptake inhibitors (SSRIs) are first-line treatment for post-traumatic stress disorder (PTSD) patients, their therapeutic efficacy is limited. Childhood adversities are considered a risk factor for developing PTSD in adulthood but may trigger PTSD without additional trauma in some individuals. Nevertheless, just as childhood is considered a vulnerable period it may also be an effective period for preventive treatment. Using a rat model of childhood-induced PTSD, pre-pubertal stress (juvenile stress, JVS), we compared the therapeutic effects of fluoxetine and examined the effectiveness of 1 month of fluoxetine treatment following JVS and into adulthood compared to treatment in adulthood. Since not all individuals develop PTSD following a trauma, comparing only group means is not the adequate type of analysis. We employed a behavioral profiling approach, which analyzes individual differences compared to the normal behavior of a control group. Animals exposed to JVS exhibited a higher proportion of affected animals as measured using the elevated plus maze 8 weeks after JVS. Fluoxetine treatment following the JVS significantly decreased the proportion of affected animals as measured in adulthood. Fluoxetine treatment in adulthood was not effective. The results support the notion that childhood is not only a vulnerable period but also an effective period for preventive treatment. Nature Publishing Group UK 2017-11-30 /pmc/articles/PMC5802710/ /pubmed/29187754 http://dx.doi.org/10.1038/s41398-017-0014-5 Text en © The Author(s) 2017 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 Ariel, Lior Inbar, Sapir Edut, Schachaf Richter-Levin, Gal Fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder |
title | Fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder |
title_full | Fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder |
title_fullStr | Fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder |
title_full_unstemmed | Fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder |
title_short | Fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder |
title_sort | fluoxetine treatment is effective in a rat model of childhood-induced post-traumatic stress disorder |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802710/ https://www.ncbi.nlm.nih.gov/pubmed/29187754 http://dx.doi.org/10.1038/s41398-017-0014-5 |
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