期刊论文详细信息
PHYSIOLOGY & BEHAVIOR 卷:219
Sex-dependent effects of chronic variable stress on discrete corticotropin-releasing factor receptor 1 cell populations
Article
Rosinger, Zachary J.1  De Guzman, Rose M.1  Jacobskind, Jason S.1  Saglimbeni, Brianna1  Malone, Margaret1  Fico, Danielle1  Justice, Nicholas J.2  Forni, Paolo E.3,4  Zuloaga, Damian G.1 
[1] Univ Albany, Dept Psychol, Albany, NY 12222 USA
[2] Univ Texas Houston, Hlth Sci Ctr, Ctr Metab & Degenerat Dis, Inst Mol Med, Houston, TX USA
[3] Univ Albany State Univ New York, Dept Biol Sci, RNA Inst, Albany, NY 12222 USA
[4] Univ Albany State Univ New York, Ctr Neurosci Res, Albany, NY 12222 USA
关键词: Corticotropin releasing factor;    Sex difference;    Chronic stress;    Anxiety;   
DOI  :  10.1016/j.physbeh.2020.112847
来源: Elsevier
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【 摘 要 】

Anxiety and depression are strikingly more prevalent in women compared with men. Dysregulation of corticotropin-releasing factor (CRF) binding to its cognate receptor (CRFR1) is thought to play a critical role in the etiology of these disorders. In the present study, we investigated whether there were sex differences in the effects of chronic variable stress (CVS) on CRFR1 cells using CRFR1-GFP reporter mice experiencing a 9-day CVS paradigm. Brains were collected from CVS and stress naive female and male mice following exposure to the open field test. This CVS paradigm effectively increased anxiety-like behavior in female and male mice. In addition, we assessed changes in activation of CRFR1 cells (co-localization with c-Fos and phosphorylated CREB (pCREB)) in stress associated brain structures, including two sexually dimorphic CRFR1 cell groups in the anteroventral periventricular nucleus (AVPV/PeN; F>M) and paraventricular hypothalamus (PVN; M>F). CVS increased CRFR1-GFP cell number as well as the number of CRFR1/pCREB co-expressing cells in the female but not male AVPV/PeN. In the PVN, the number of CRFR1/pCREB co-expressing cells was overall greater in males regardless of treatment and CVS resulted in a male-specific reduction of CRFR1/c-Fos cells. In addition, CVS induced a female-specific reduction in CRFR1/c-Fos cells within the anteroventral bed nucleus of the stria terminalis and both sexes exhibited a reduction in CRFR1/c-Fos co-expressing cells following CVS within the ventral basolateral amygdala. Overall, these sex-specific effects of CVS on CRFR1 populations may have implications for sex differences in stress-induction of mood disorders.

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