Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Nov 1:256:520-8.
doi: 10.1016/j.bbr.2013.09.002. Epub 2013 Sep 7.

Serotonergic receptor mechanisms underlying antidepressant-like action in the progesterone withdrawal model of hormonally induced depression in rats

Affiliations

Serotonergic receptor mechanisms underlying antidepressant-like action in the progesterone withdrawal model of hormonally induced depression in rats

Yan Li et al. Behav Brain Res. .

Abstract

Hormonally induced mood disorders such as premenstrual dysphoric disorder (PMDD) are characterized by a range of physical and affective symptoms including anxiety, irritability, anhedonia, social withdrawal and depression. Studies demonstrated rodent models of progesterone withdrawal (PWD) have a high level of constructive and descriptive validity to model hormonally-induced mood disorders in women. Here we evaluate the effects of several classes of antidepressants in PWD female Long-Evans rats using the forced swim test (FST) as a measure of antidepressant activity. The study included fluoxetine, duloxetine, amitriptyline and an investigational multimodal antidepressant, vortioxetine (5-HT(3), 5-HT(7) and 5-HT(1D) receptor antagonist; 5-HT(1B) receptor partial agonist; 5-HT(1A) receptor agonist; inhibitor of the serotonin transporter (SERT)). After 14 days of administration, amitriptyline and vortioxetine significantly reduced immobility in the FST whereas fluoxetine and duloxetine were ineffective. After 3 injections over 48 h, neither fluoxetine nor duloxetine reduced immobility, whereas amitriptyline and vortioxetine significantly reduced FST immobility during PWD. When administered acutely during PWD, the 5-HT(1A) receptor agonist, flesinoxan, significantly reduced immobility, whereas the 5-HT(1A) receptor antagonist, WAY-100635, increased immobility. The 5-HT(3) receptor antagonist, ondansetron, significantly reduced immobility, whereas the 5-HT(3) receptor agonist, SR-57227, increased immobility. The 5-HT(7) receptor antagonist, SB-269970, was inactive, although the 5-HT(7) receptor agonist, AS-19, significantly increased PWD-induced immobility. None of the compounds investigated (ondansetron, flesinoxan and SB-269970) improved the effect of fluoxetine during PWD. These data indicate that modulation of specific 5-HT receptor subtypes is critical for manipulating FST immobility in this model of hormone-induced depression.

Keywords: 5-HT; 8-OH-DPAT DPAT; 8-hydroxy-2-(di-N-propylamino)tetralin; AMI; ANOVA; AS; AS-19; DLX; FLES; FLX; FST; Flesinoxan; Forced swim test; GABA; OND; Ondansetron; PMDD; PWD; Premenstrual dysphoric disorder (PMDD); Progesterone withdrawal; SB; SB-269970; SERT; SNRI; SR; SR-57227; SSRI; VOR; Vortioxetine; WAY; WAY-100635; amitriptyline; analysis of variance; duloxetine; flesinoxan; fluoxetine; forced swim test; ondansetron; premenstrual dysphoric disorder; progesterone withdrawal; selective serotonin reuptake inhibitor; serotonin; serotonin norepinephrine reuptake inhibitor; serotonin transporter; vortioxetine; γ-aminobutyric acid.

PubMed Disclaimer

Similar articles

Cited by

Publication types