Evidence map›Paper›PMID 35150728›Full record

ArticlePharmacology, biochemistry, and behavior2022

Acute administration of fluoxetine increases social avoidance and risk assessment behaviors in a sex- and social stress-dependent manner in Syrian hamsters (Mesocricetus auratus).

Zachary A Grieb, Dené A Voisin, Joseph I Terranova, Alisa Norvelle, Vasiliki Michopoulos, Kim L Huhman, H Elliott Albers

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 45% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Zachary A GriebNeuroscience Institute, Georgia State University, Atlanta, GA, United States of America. Electronic address: zgrieb1@gsu.edu.
Dené A VoisinNeuroscience Institute, Georgia State University, Atlanta, GA, United States of America.
Joseph I TerranovaNeuroscience Institute, Georgia State University, Atlanta, GA, United States of America; Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, United States of America.
Alisa NorvelleNeuroscience Institute, Georgia State University, Atlanta, GA, United States of America.
Vasiliki MichopoulosYerkes National Primate Center, Atlanta, GA, United States of America; Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, United States of America.
Kim L HuhmanNeuroscience Institute, Georgia State University, Atlanta, GA, United States of America.
H Elliott AlbersNeuroscience Institute, Georgia State University, Atlanta, GA, United States of America.
Georgia State University · USEmory University · USThe University of Texas Southwestern Medical Center · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Sex Differences in the Social BrainR01MH110212 · NIMH · GEORGIA STATE UNIVERSITY · PI ALBERS, H. ELLIOTT, MICHOPOULOS, VASILIKI · 2016 to 2020
$3.3M
Sex-dependent regulation of social reward by oxytocin in the mesolimbic reward circuitryR01MH122622 · NIMH · GEORGIA STATE UNIVERSITY · PI ALBERS, H. ELLIOTT, HUHMAN, KIM L · 2021 to 2025
$2.7M
NIH HHS P51 OD011132NIMH NIH HHS R01 MH110212NIMH NIH HHS R01 MH122622
6 · The paper itself

Abstract

Most studies investigating the effects of acute administration of selective serotonin reuptake inhibitors (SSRI) on responses to social stress have been conducted with males. This is despite the fact that SSRIs remain the primary pharmacotherapy for social stress-related disorders for both sexes and that the prevalence of these disorders is twofold higher in women than in men. To determine whether acute treatment with the SSRI, fluoxetine, alters behavioral responses to social defeat stress in a sex- or social stress-dependent manner, male and female Syrian hamsters were subjected to one of three social defeat conditions: no defeat (placed into an empty resident aggressor (RA) cage), a single defeat by one RA for 15 min, or three consecutive defeats using different RAs for 5 min each. The day following social defeat, subjects were infused with either vehicle or fluoxetine (20 mg/kg, I.P.) 2 h prior to a 5 min social avoidance test. Overall, we found that fluoxetine increased social vigilance regardless of sex or defeat condition. We also found that fluoxetine affected social avoidance in a sex by stress intensity interaction, such that fluoxetine increased avoidance in no defeat males and in males defeated once but significantly increased avoidance in females only after three defeats. These data suggest that treatment with an SSRI could initially exacerbate the effects of social stress in both sexes. These data also emphasize the importance of including sex as a biological variable when investigating the efficacy of pharmacotherapy for stress-related disorders.

Indexed as

FluoxetineSocial BehaviorAnimalsBehavior, AnimalCricetinaeFemaleHumansMaleMesocricetusRisk AssessmentSelective Serotonin Reuptake InhibitorsStress, PsychologicalFluoxetineSelective Serotonin Reuptake InhibitorsAvoidanceFluoxetineSex differencesSocial defeatSocial stressSSRIVigilance

Identifiers

PMID35150728
PMCPMC8915384
OpenAlexW4210850696

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.