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The effects of sex and hormonal status on restraint-stress-induced working memory impairment

BACKGROUND: Restraint stress has been shown to elicit numerous effects on hippocampal function and neuronal morphology, as well as to induce dendritic remodeling in the prefrontal cortex (PFC). However, the effects of acute restraint stress on PFC cognitive function have not been investigated, despi...

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Autores principales: Shansky, Rebecca M, Rubinow, Katya, Brennan, Avis, Arnsten, Amy FT
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1420310/
https://www.ncbi.nlm.nih.gov/pubmed/16522198
http://dx.doi.org/10.1186/1744-9081-2-8
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author Shansky, Rebecca M
Rubinow, Katya
Brennan, Avis
Arnsten, Amy FT
author_facet Shansky, Rebecca M
Rubinow, Katya
Brennan, Avis
Arnsten, Amy FT
author_sort Shansky, Rebecca M
collection PubMed
description BACKGROUND: Restraint stress has been shown to elicit numerous effects on hippocampal function and neuronal morphology, as well as to induce dendritic remodeling in the prefrontal cortex (PFC). However, the effects of acute restraint stress on PFC cognitive function have not been investigated, despite substantial evidence that the PFC malfunctions in many stress-related disorders. METHODS: The present study examined the effects of restraint stress on PFC function in both male rats and cycling female rats in either the proestrus (high estrogen) or estrus (low estrogen) phase of the estrus cycle. Animals were restrained for 60 or 120 minutes and then tested on spatial delayed alternation, a PFC-mediated task. Performance after stress was compared to performance on a different day under no-stress conditions, and analyzed using analysis of variance (ANOVA). RESULTS: Sixty minutes of restraint impaired only females in proestrus, while 120 minutes of restraint produced significant impairments in all animals. Increases in task completion times did not affect performance. CONCLUSION: These results demonstrate an interaction between hormonal status and cognitive response to stress in female rats, with high estrogen levels being associated with amplified sensitivity to stress. This effect has been previously observed after administration of a pharmacological stressor (the benzodiazepine inverse agonist FG7142), and results from both studies may be relevant to the increased prevalence of stress-related disorders, such as major depressive disorder, in cycling women. Overall, the results show that restraint stress has important effects on the cognitive functions of the PFC, and that hormonal influences in the PFC are an important area for future research.
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spelling pubmed-14203102006-03-30 The effects of sex and hormonal status on restraint-stress-induced working memory impairment Shansky, Rebecca M Rubinow, Katya Brennan, Avis Arnsten, Amy FT Behav Brain Funct Research BACKGROUND: Restraint stress has been shown to elicit numerous effects on hippocampal function and neuronal morphology, as well as to induce dendritic remodeling in the prefrontal cortex (PFC). However, the effects of acute restraint stress on PFC cognitive function have not been investigated, despite substantial evidence that the PFC malfunctions in many stress-related disorders. METHODS: The present study examined the effects of restraint stress on PFC function in both male rats and cycling female rats in either the proestrus (high estrogen) or estrus (low estrogen) phase of the estrus cycle. Animals were restrained for 60 or 120 minutes and then tested on spatial delayed alternation, a PFC-mediated task. Performance after stress was compared to performance on a different day under no-stress conditions, and analyzed using analysis of variance (ANOVA). RESULTS: Sixty minutes of restraint impaired only females in proestrus, while 120 minutes of restraint produced significant impairments in all animals. Increases in task completion times did not affect performance. CONCLUSION: These results demonstrate an interaction between hormonal status and cognitive response to stress in female rats, with high estrogen levels being associated with amplified sensitivity to stress. This effect has been previously observed after administration of a pharmacological stressor (the benzodiazepine inverse agonist FG7142), and results from both studies may be relevant to the increased prevalence of stress-related disorders, such as major depressive disorder, in cycling women. Overall, the results show that restraint stress has important effects on the cognitive functions of the PFC, and that hormonal influences in the PFC are an important area for future research. BioMed Central 2006-03-07 /pmc/articles/PMC1420310/ /pubmed/16522198 http://dx.doi.org/10.1186/1744-9081-2-8 Text en Copyright © 2006 Shansky et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Shansky, Rebecca M
Rubinow, Katya
Brennan, Avis
Arnsten, Amy FT
The effects of sex and hormonal status on restraint-stress-induced working memory impairment
title The effects of sex and hormonal status on restraint-stress-induced working memory impairment
title_full The effects of sex and hormonal status on restraint-stress-induced working memory impairment
title_fullStr The effects of sex and hormonal status on restraint-stress-induced working memory impairment
title_full_unstemmed The effects of sex and hormonal status on restraint-stress-induced working memory impairment
title_short The effects of sex and hormonal status on restraint-stress-induced working memory impairment
title_sort effects of sex and hormonal status on restraint-stress-induced working memory impairment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1420310/
https://www.ncbi.nlm.nih.gov/pubmed/16522198
http://dx.doi.org/10.1186/1744-9081-2-8
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