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Sexually Dimorphic Risk Mitigation Strategies in Rats

The scientific understanding of fear and anxiety—in both normal and pathological forms—is presently limited by a predominance of studies that use male animals and Pavlovian fear conditioning-centered paradigms that restrict and assess specific behaviors (e.g., freezing) over brief sampling periods a...

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Autores principales: Pellman, Blake A., Schuessler, Bryan P., Tellakat, Mohini, Kim, Jeansok J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292597/
https://www.ncbi.nlm.nih.gov/pubmed/28197550
http://dx.doi.org/10.1523/ENEURO.0288-16.2017
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author Pellman, Blake A.
Schuessler, Bryan P.
Tellakat, Mohini
Kim, Jeansok J.
author_facet Pellman, Blake A.
Schuessler, Bryan P.
Tellakat, Mohini
Kim, Jeansok J.
author_sort Pellman, Blake A.
collection PubMed
description The scientific understanding of fear and anxiety—in both normal and pathological forms—is presently limited by a predominance of studies that use male animals and Pavlovian fear conditioning-centered paradigms that restrict and assess specific behaviors (e.g., freezing) over brief sampling periods and overlook the broader contributions of the spatiotemporal context to an animal’s behavioral responses to threats. Here, we use a risky “closed economy” system, in which the need to acquire food and water and the need to avoid threats are simultaneously integrated into the lives of rats, to examine sex differences in mitigating threat risk while foraging. Rats lived for an extended period (∼2 months) in enlarged chambers that consisted of a safe, bedded nest and a risky foraging area where footshocks could be delivered unpredictably. We observed that male and female rats used different strategies for responding to the threat of footshock. Whereas male rats increased the size of meals consumed to reduce the overall time spent foraging, female rats sacrificed their metabolic needs in order to avoid shocks. Ovarian hormone fluctuations were shown to exert slight but reliable rhythmic effects on risky decision-making in gonadally intact female rats. However, this did not produce significant differences in approach–avoidance trade-offs between ovariectomized and intact female groups, suggesting that male–female sex differences are not due to the activational effects of gonadal hormones but, rather, are likely to be organized during early development.
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spelling pubmed-52925972017-02-14 Sexually Dimorphic Risk Mitigation Strategies in Rats Pellman, Blake A. Schuessler, Bryan P. Tellakat, Mohini Kim, Jeansok J. eNeuro New Research The scientific understanding of fear and anxiety—in both normal and pathological forms—is presently limited by a predominance of studies that use male animals and Pavlovian fear conditioning-centered paradigms that restrict and assess specific behaviors (e.g., freezing) over brief sampling periods and overlook the broader contributions of the spatiotemporal context to an animal’s behavioral responses to threats. Here, we use a risky “closed economy” system, in which the need to acquire food and water and the need to avoid threats are simultaneously integrated into the lives of rats, to examine sex differences in mitigating threat risk while foraging. Rats lived for an extended period (∼2 months) in enlarged chambers that consisted of a safe, bedded nest and a risky foraging area where footshocks could be delivered unpredictably. We observed that male and female rats used different strategies for responding to the threat of footshock. Whereas male rats increased the size of meals consumed to reduce the overall time spent foraging, female rats sacrificed their metabolic needs in order to avoid shocks. Ovarian hormone fluctuations were shown to exert slight but reliable rhythmic effects on risky decision-making in gonadally intact female rats. However, this did not produce significant differences in approach–avoidance trade-offs between ovariectomized and intact female groups, suggesting that male–female sex differences are not due to the activational effects of gonadal hormones but, rather, are likely to be organized during early development. Society for Neuroscience 2017-02-06 /pmc/articles/PMC5292597/ /pubmed/28197550 http://dx.doi.org/10.1523/ENEURO.0288-16.2017 Text en Copyright © 2017 Pellman et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Pellman, Blake A.
Schuessler, Bryan P.
Tellakat, Mohini
Kim, Jeansok J.
Sexually Dimorphic Risk Mitigation Strategies in Rats
title Sexually Dimorphic Risk Mitigation Strategies in Rats
title_full Sexually Dimorphic Risk Mitigation Strategies in Rats
title_fullStr Sexually Dimorphic Risk Mitigation Strategies in Rats
title_full_unstemmed Sexually Dimorphic Risk Mitigation Strategies in Rats
title_short Sexually Dimorphic Risk Mitigation Strategies in Rats
title_sort sexually dimorphic risk mitigation strategies in rats
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292597/
https://www.ncbi.nlm.nih.gov/pubmed/28197550
http://dx.doi.org/10.1523/ENEURO.0288-16.2017
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