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The Stage of the Estrus Cycle Is Critical for Interpretation of Female Mouse Social Interaction Behavior

Female animals in biomedical research have traditionally been excluded from research studies due to the perceived added complexity caused by the estrus cycle. However, given the importance of sex differences in a variety of neurological disorders, testing female mice is critical to identifying sex-l...

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Autores principales: Chari, Trishala, Griswold, Sophie, Andrews, Nick A., Fagiolini, Michela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340104/
https://www.ncbi.nlm.nih.gov/pubmed/32714163
http://dx.doi.org/10.3389/fnbeh.2020.00113
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author Chari, Trishala
Griswold, Sophie
Andrews, Nick A.
Fagiolini, Michela
author_facet Chari, Trishala
Griswold, Sophie
Andrews, Nick A.
Fagiolini, Michela
author_sort Chari, Trishala
collection PubMed
description Female animals in biomedical research have traditionally been excluded from research studies due to the perceived added complexity caused by the estrus cycle. However, given the importance of sex differences in a variety of neurological disorders, testing female mice is critical to identifying sex-linked effects in diseases. To determine the susceptibility of simple behaviors to hormonal fluctuations in the estrus cycle, we studied the effects of sex and the estrus cycle on a variety of behavioral tasks commonly used in mouse phenotyping laboratories. Male and female C57BL/6J mice were tested in a small battery of short duration tests and, immediately on completion of each test, females were classified using cytology of vaginal lavages as sexually-receptive (proestrus and estrus) or non-receptive (NR; metestrus and diestrus). We showed that there was a significant difference in 3-chamber social interaction (SI) between female mice at different stages of their estrus cycle, with sexually-receptive mice showing no preferential interest in a novel female mouse compared with an empty chamber. NR female mice showed the same level of preference for a novel female mouse as male mice did for a novel male mouse. No differences between or within sexes were found for tests of anxiety elevated plus maze (EPM; Hole board), working memory [Novel object recognition (NOR)], and motor learning (repeated tests on rotarod). We conclude that the stage of the estrus cycle may impact SI between same-sex conspecifics, and does not impact performance in the elevated plus-maze, hole board, NOR, and rotarod.
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spelling pubmed-73401042020-07-23 The Stage of the Estrus Cycle Is Critical for Interpretation of Female Mouse Social Interaction Behavior Chari, Trishala Griswold, Sophie Andrews, Nick A. Fagiolini, Michela Front Behav Neurosci Behavioral Neuroscience Female animals in biomedical research have traditionally been excluded from research studies due to the perceived added complexity caused by the estrus cycle. However, given the importance of sex differences in a variety of neurological disorders, testing female mice is critical to identifying sex-linked effects in diseases. To determine the susceptibility of simple behaviors to hormonal fluctuations in the estrus cycle, we studied the effects of sex and the estrus cycle on a variety of behavioral tasks commonly used in mouse phenotyping laboratories. Male and female C57BL/6J mice were tested in a small battery of short duration tests and, immediately on completion of each test, females were classified using cytology of vaginal lavages as sexually-receptive (proestrus and estrus) or non-receptive (NR; metestrus and diestrus). We showed that there was a significant difference in 3-chamber social interaction (SI) between female mice at different stages of their estrus cycle, with sexually-receptive mice showing no preferential interest in a novel female mouse compared with an empty chamber. NR female mice showed the same level of preference for a novel female mouse as male mice did for a novel male mouse. No differences between or within sexes were found for tests of anxiety elevated plus maze (EPM; Hole board), working memory [Novel object recognition (NOR)], and motor learning (repeated tests on rotarod). We conclude that the stage of the estrus cycle may impact SI between same-sex conspecifics, and does not impact performance in the elevated plus-maze, hole board, NOR, and rotarod. Frontiers Media S.A. 2020-06-30 /pmc/articles/PMC7340104/ /pubmed/32714163 http://dx.doi.org/10.3389/fnbeh.2020.00113 Text en Copyright © 2020 Chari, Griswold, Andrews and Fagiolini. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Behavioral Neuroscience
Chari, Trishala
Griswold, Sophie
Andrews, Nick A.
Fagiolini, Michela
The Stage of the Estrus Cycle Is Critical for Interpretation of Female Mouse Social Interaction Behavior
title The Stage of the Estrus Cycle Is Critical for Interpretation of Female Mouse Social Interaction Behavior
title_full The Stage of the Estrus Cycle Is Critical for Interpretation of Female Mouse Social Interaction Behavior
title_fullStr The Stage of the Estrus Cycle Is Critical for Interpretation of Female Mouse Social Interaction Behavior
title_full_unstemmed The Stage of the Estrus Cycle Is Critical for Interpretation of Female Mouse Social Interaction Behavior
title_short The Stage of the Estrus Cycle Is Critical for Interpretation of Female Mouse Social Interaction Behavior
title_sort stage of the estrus cycle is critical for interpretation of female mouse social interaction behavior
topic Behavioral Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340104/
https://www.ncbi.nlm.nih.gov/pubmed/32714163
http://dx.doi.org/10.3389/fnbeh.2020.00113
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