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dc.contributor.authorLaClair, M.
dc.contributor.authorFebo, M.
dc.contributor.authorNephew, Ben
dc.contributor.authorGervais, N. J.
dc.contributor.authorPoirier, G.
dc.contributor.authorWorkman, K.
dc.contributor.authorChumachenko, Serhiy
dc.contributor.authorPayne, L.
dc.contributor.authorMoore, Constance M.
dc.contributor.authorKing, Jean A.
dc.contributor.authorLacreuse, A.
dc.date2022-08-11T08:09:53.000
dc.date.accessioned2022-08-23T16:47:40Z
dc.date.available2022-08-23T16:47:40Z
dc.date.issued2019-07-25
dc.date.submitted2019-08-09
dc.identifier.citation<p>eNeuro. 2019 Jul 25;6(4). pii: ENEURO.0154-19.2019. doi: 10.1523/ENEURO.0154-19.2019. Print 2019 Jul/Aug. <a href="https://doi.org/10.1523/ENEURO.0154-19.2019">Link to article on publisher's site</a></p>
dc.identifier.issn2373-2822 (Linking)
dc.identifier.doi10.1523/ENEURO.0154-19.2019
dc.identifier.pmid31262949
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41126
dc.description.abstractSex differences in human cognitive performance are well characterized. However, the neural correlates of these differences remain elusive. This issue may be clarified using nonhuman primates, for which sociocultural influences are minimized. We used the marmoset (Callithrix jacchus) to investigate sex differences in two aspects of executive function: reversal learning and intradimensional/extradimensional (ID/ED) set shifting. Stress reactivity and motor function were also assessed. In agreement with human literature, females needed more trials than males to acquire the reversals. No sex differences in ED set shifting or motivational measures were observed. The findings suggest enhanced habit formation in females, perhaps due to striatal estrogenic effects. Both sexes showed increased urinary cortisol during social separation stressor, but females showed an earlier increase in cortisol and a greater increase in agitated locomotion, possibly indicating enhanced stress reactivity. Independent of sex, basal cortisol predicted cognitive performance. No sex differences were found in motor performance. Associations between brain networks and reversal learning performance were investigated using resting state fMRI. Resting state functional connectivity (rsFC) analyses revealed sex differences in cognitive networks, with differences in overall neural network metrics and specific regions, including the prefrontal cortex, caudate, putamen, and nucleus accumbens. Correlations between cognitive flexibility and neural connectivity indicate that sex differences in cognitive flexibility are related to sex-dependent patterns of resting brain networks. Overall, our findings reveal sex differences in reversal learning, brain networks, and their relationship in the marmoset, positioning this species as an excellent model to investigate the biological basis of cognitive sex differences.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=31262949&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright © 2019 LaClair et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectanimal models
dc.subjectcognitive flexibility
dc.subjectexecutive function
dc.subjectresting state functional connectivity
dc.subjectreversal learning
dc.subjectsex differences
dc.subjectCognitive Neuroscience
dc.subjectGender and Sexuality
dc.subjectNervous System
dc.subjectPsychiatry
dc.subjectPsychiatry and Psychology
dc.titleSex Differences in Cognitive Flexibility and Resting Brain Networks in Middle-Aged Marmosets
dc.typeJournal Article
dc.source.journaltitleeNeuro
dc.source.volume6
dc.source.issue4
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4931&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3915
dc.identifier.contextkey15087834
refterms.dateFOA2022-08-23T16:47:40Z
html.description.abstract<p>Sex differences in human cognitive performance are well characterized. However, the neural correlates of these differences remain elusive. This issue may be clarified using nonhuman primates, for which sociocultural influences are minimized. We used the marmoset (Callithrix jacchus) to investigate sex differences in two aspects of executive function: reversal learning and intradimensional/extradimensional (ID/ED) set shifting. Stress reactivity and motor function were also assessed. In agreement with human literature, females needed more trials than males to acquire the reversals. No sex differences in ED set shifting or motivational measures were observed. The findings suggest enhanced habit formation in females, perhaps due to striatal estrogenic effects. Both sexes showed increased urinary cortisol during social separation stressor, but females showed an earlier increase in cortisol and a greater increase in agitated locomotion, possibly indicating enhanced stress reactivity. Independent of sex, basal cortisol predicted cognitive performance. No sex differences were found in motor performance. Associations between brain networks and reversal learning performance were investigated using resting state fMRI. Resting state functional connectivity (rsFC) analyses revealed sex differences in cognitive networks, with differences in overall neural network metrics and specific regions, including the prefrontal cortex, caudate, putamen, and nucleus accumbens. Correlations between cognitive flexibility and neural connectivity indicate that sex differences in cognitive flexibility are related to sex-dependent patterns of resting brain networks. Overall, our findings reveal sex differences in reversal learning, brain networks, and their relationship in the marmoset, positioning this species as an excellent model to investigate the biological basis of cognitive sex differences.</p>
dc.identifier.submissionpathoapubs/3915
dc.contributor.departmentDepartment of Psychiatry
dc.contributor.departmentCenter for Comparative Neuroimaging
dc.source.pagesENEURO.0154-19.2019


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Copyright © 2019 LaClair et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
Except where otherwise noted, this item's license is described as Copyright © 2019 LaClair et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.