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Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation

The role of sex and androgen receptors (ARs) for social preference and social memory is rather unknown. In this study of mice we compared males, females and males lacking ARs specifically in the nervous system, AR(NesDel), with respect to social preference, assessed with the three-chambered apparatu...

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Autores principales: Karlsson, Sara A., Studer, Erik, Kettunen, Petronella, Westberg, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792870/
https://www.ncbi.nlm.nih.gov/pubmed/27014003
http://dx.doi.org/10.3389/fnbeh.2016.00041
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author Karlsson, Sara A.
Studer, Erik
Kettunen, Petronella
Westberg, Lars
author_facet Karlsson, Sara A.
Studer, Erik
Kettunen, Petronella
Westberg, Lars
author_sort Karlsson, Sara A.
collection PubMed
description The role of sex and androgen receptors (ARs) for social preference and social memory is rather unknown. In this study of mice we compared males, females and males lacking ARs specifically in the nervous system, AR(NesDel), with respect to social preference, assessed with the three-chambered apparatus test, and social recognition, assessed with the social discrimination procedure. In the social discrimination test we also evaluated the tentative importance of the sex of the stimulus animal. Novel object recognition and olfaction were investigated to complement the results from the social tests. Gene expression analysis was performed to reveal molecules involved in the effects of sex and androgens on social behaviors. All three test groups showed social preference in the three-chambered apparatus test. In both social tests an AR-independent sexual dimorphism was seen in the persistence of social investigation of female conspecifics, whereas the social interest toward male stimuli mice was similar in all groups. Male and female controls recognized conspecifics independent of their sex, whereas AR(NesDel) males recognized female but not male stimuli mice. Moreover, the non-social behaviors were not affected by AR deficiency. The gene expression analyses of hypothalamus and amygdala indicated that Oxtr, Cd38, Esr1, Cyp19a1, Ucn3, Crh, and Gtf2i were differentially expressed between the three groups. In conclusion, our results suggest that ARs are required for recognition of male but not female conspecifics, while being dispensable for social investigation toward both sexes. In addition, the AR seems to regulate genes related to oxytocin, estrogen and William’s syndrome.
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spelling pubmed-47928702016-03-24 Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation Karlsson, Sara A. Studer, Erik Kettunen, Petronella Westberg, Lars Front Behav Neurosci Neuroscience The role of sex and androgen receptors (ARs) for social preference and social memory is rather unknown. In this study of mice we compared males, females and males lacking ARs specifically in the nervous system, AR(NesDel), with respect to social preference, assessed with the three-chambered apparatus test, and social recognition, assessed with the social discrimination procedure. In the social discrimination test we also evaluated the tentative importance of the sex of the stimulus animal. Novel object recognition and olfaction were investigated to complement the results from the social tests. Gene expression analysis was performed to reveal molecules involved in the effects of sex and androgens on social behaviors. All three test groups showed social preference in the three-chambered apparatus test. In both social tests an AR-independent sexual dimorphism was seen in the persistence of social investigation of female conspecifics, whereas the social interest toward male stimuli mice was similar in all groups. Male and female controls recognized conspecifics independent of their sex, whereas AR(NesDel) males recognized female but not male stimuli mice. Moreover, the non-social behaviors were not affected by AR deficiency. The gene expression analyses of hypothalamus and amygdala indicated that Oxtr, Cd38, Esr1, Cyp19a1, Ucn3, Crh, and Gtf2i were differentially expressed between the three groups. In conclusion, our results suggest that ARs are required for recognition of male but not female conspecifics, while being dispensable for social investigation toward both sexes. In addition, the AR seems to regulate genes related to oxytocin, estrogen and William’s syndrome. Frontiers Media S.A. 2016-03-16 /pmc/articles/PMC4792870/ /pubmed/27014003 http://dx.doi.org/10.3389/fnbeh.2016.00041 Text en Copyright © 2016 Karlsson, Studer, Kettunen and Westberg. 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) or licensor 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 Neuroscience
Karlsson, Sara A.
Studer, Erik
Kettunen, Petronella
Westberg, Lars
Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation
title Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation
title_full Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation
title_fullStr Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation
title_full_unstemmed Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation
title_short Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation
title_sort neural androgen receptors modulate gene expression and social recognition but not social investigation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4792870/
https://www.ncbi.nlm.nih.gov/pubmed/27014003
http://dx.doi.org/10.3389/fnbeh.2016.00041
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