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Sex differences in the effect of the FKBP5 inhibitor SAFit2 on anxiety and stress-induced reinstatement following cocaine self-administration
Author(s) -
Krista L. Connelly,
Cassandra Wolsh,
Jeffrey L. Barr,
Michael Bauder,
Felix Hausch,
Ellen M. Unterwald
Publication year - 2020
Publication title -
neurobiology of stress
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.481
H-Index - 33
ISSN - 2352-2895
DOI - 10.1016/j.ynstr.2020.100232
Subject(s) - self administration , fkbp5 , anxiety , psychology , medicine , pharmacology , glucocorticoid , glucocorticoid receptor , psychiatry
Cocaine use and withdrawal prompt stress system responses. Stress and the negative affective state produced by cocaine withdrawal are major triggers for relapse. FKBP5 is a co-chaperone of the glucocorticoid receptor and regulates HPA axis negative feedback. The role of FKBP5 in cocaine-related behaviors has not been studied. The FKBP5 inhibitor SAFit2 was used to examine the role of FKBP5 in anxiety-like behavior during early cocaine withdrawal and in stress-induced reinstatement following cocaine self-administration in male and female rats. Withdrawal from cocaine self-administration resulted in heightened anxiety-like behavior in female rats, which was significantly attenuated by SAFit2 administration. SAFit2 pretreatment prior to stress-induced reinstatement to cocaine seeking significantly reduced active lever presses of males. In female rats, SAFit2 administration prevented stress-induced reinstatement for rats in metestrus or diestrus, but not proestrus or estrus phases at the time of reinstatement. These data suggest an important role for FKBP5 in stress-related behaviors following cocaine self-administration, particularly in females.

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