Evidence map›Paper›PMID 28284881›Full record

ArticlePhysiology & behavior2017

Susceptibility or resilience? Prenatal stress predisposes male rats to social subordination, but facilitates adaptation to subordinate status.

Karen A Scott, Annette D de Kloet, Michael D Smeltzer, Eric G Krause, Jonathan N Flak, Susan J Melhorn, Michelle T Foster, Kellie L K Tamashiro, Randall R Sakai

Open access · greenAbstract read
In one paragraph

Article in Physiology & behavior, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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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

9 authors at 3 institutions in 1 country.

Karen A ScottDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA; Graduate Program in Neuroscience, University of Cincinnati, Cincinnati 45237, USA. Electronic address: k.scott@ucc.ie.
Annette D de KloetDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA; Graduate Program in Neuroscience, University of Cincinnati, Cincinnati 45237, USA.
Michael D SmeltzerDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA.
Eric G KrauseDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA.
Jonathan N FlakDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA; Graduate Program in Neuroscience, University of Cincinnati, Cincinnati 45237, USA.
Susan J MelhornDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA; Graduate Program in Neuroscience, University of Cincinnati, Cincinnati 45237, USA.
Michelle T FosterDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA.
Kellie L K TamashiroDepartment of Psychiatry & Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Randall R SakaiDepartment of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH 45237, USA.
University of Cincinnati · USUniversity of Cincinnati Medical Center · USJohns Hopkins Medicine · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Wendy M Kohrt · 1995 to 2026
$32.6M
University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OWYANG, CHUNG · 1986 to 2021
$22.5M
Training in Basic and Translational Digestive SciencesT32DK094775 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JOHN Y KAO, LINDA C. SAMUELSON · 2012 to 2026
$3.6M
Stress and Body Weight RegulationR01DK066596 · NIDDK · UNIVERSITY OF CINCINNATI · PI SAKAI, RANDALL R. · 2004 to 2011
$2.7M
Food intake and obesity in cloned miceR01DK068273 · NIDDK · UNIVERSITY OF CINCINNATI · PI SAKAI, RANDALL R. · 2006 to 2010
$1.8M
Impact of multiple stress exposures on susceptibility to depressive-like symptomsF31MH088230 · NIMH · UNIVERSITY OF CINCINNATI · PI SCOTT, KAREN ANN · 2010 to 2011
$68k
NIDDK NIH HHS P30 DK034933NIDDK NIH HHS P30 DK048520NIDDK NIH HHS R01 DK066596NIDDK NIH HHS R01 DK068273NIDDK NIH HHS T32 DK094775NIMH NIH HHS F31 MH088230
6 · The paper itself

Abstract

Mood disorders such as major depressive disorder (MDD) affect a significant proportion of the population. Although progress has been made in the development of therapeutics, a large number of individuals do not attain full remission of symptoms and adverse side effects affect treatment compliance for some. In order to develop new therapies, there is a push for new models that better reflect the multiple risk factors that likely contribute to the development of depressive illness. We hypothesized that early life stress would exacerbate the depressive-like phenotype that we have previously observed in socially subordinate (SUB) adult male rats in the visible burrow system (VBS), a semi-natural, ethologically relevant environment in which males in a colony form a dominance hierarchy. Dams were exposed to chronic variable stress (CVS) during the last week of gestation, resulting in a robust and non-habituating glucocorticoid response that did not alter maternal food intake, body weight or litter size and weight. As adults, one prenatal CVS (PCVS) and one non-stressed (NS) male were housed in the VBS with adult females. Although there were no overt differences between PCVS and NS male offspring prior to VBS housing, a greater percentage of PCVS males became SUB. However, the depressive-like phenotype of SUB males was not exacerbated in PCVS males; rather, they appeared to better cope with SUB status than NS SUB males. They had lower basal plasma corticosterone than NS SUB males at the end of VBS housing. In situ hybridization for CRH in the PVN and CeA did not reveal any prenatal treatment or status effects, while NPY expression was higher within the MeA of dominant and subordinate males exposed to the VBS in comparison with controls, but with no effect of prenatal treatment. These data suggest that prenatal chronic variable stress may confer resilience to offspring when exposed to social stress in adulthood.

Indexed as

Adaptation, PsychologicalDominance-SubordinationResilience, PsychologicalAdrenal GlandsAnimalsBehavior, AnimalBrainCorticosteroneDepressionFemaleHousing, AnimalMaleOrgan SizePregnancyPrenatal Exposure Delayed EffectsPsychological TestsCorticosteroneRNA, MessengerTestosterone

Identifiers

PMID28284881
PMCPMC5513742
OpenAlexW2593198557

What OpenQuestion holds

Textmetadata
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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.