Evidence map›Paper›PMID 40230624›Full record

ArticleNeurobiology of stress2025

Distinguishing neural ensembles in the infralimbic cortex that regulate stress vulnerability and coping behavior.

Jenna L Laymon, Conner J Whitten, Anna F Radford, Alonnah R Brewer, Yash S Deo, Mackenzie K Hooker, Akhil A Geddati, Matthew A Cooper

Abstract read
In one paragraph

Article in Neurobiology of stress, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

8 authors.

Jenna L LaymonTranslational Neuroscience Program, Wayne State University School of Medicine, USA.
Conner J WhittenDepartment of Psychology, University of Tennessee Knoxville, USA.
Anna F RadfordDepartment of Psychology, University of Tennessee Knoxville, USA.
Alonnah R BrewerDepartment of Psychology, University of Tennessee Knoxville, USA.
Yash S DeoDepartment of Psychology, University of Tennessee Knoxville, USA.
Mackenzie K HookerDepartment of Psychology, University of Tennessee Knoxville, USA.
Akhil A GeddatiDepartment of Psychology, University of Tennessee Knoxville, USA.
Matthew A CooperDepartment of Psychology, University of Tennessee Knoxville, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neural ensembles in the medial prefrontal cortex regulate several types of responses to stress. We used a Syrian hamster model to investigate the role of infralimbic (IL) neurons in coping with social defeat stress and vulnerability to subsequent anxiety-like behavior. We created social dominance relationships in male and female hamsters, used a robust activity marker (RAM) approach to label IL neural ensembles activated during social defeat stress, and employed light-dark (LD), social avoidance (SA), and conditioned defeat (CD) tests to assess anxiety-like behavior. We found that dominant animals were less anxious in LD tests compared to subordinate animals after achieving their higher status. Also, status-dependent differences in anxiety-like behavior were maintained following social defeat in males, but not females. Subordinate males showed greater RAM-mKate2 expression in IL parvalbumin (PV) cells during social defeat exposure compared to dominant males, and submissive behavior during CD testing was correlated with RAM/PV co-expression. In contrast, greater RAM-mKate2 expression in IL neurons was correlated with a longer latency to submit during social defeat in dominant females, although the correlation of RAM/PV co-expression and defeat-induced anxiety in females was mixed. Overall, these findings suggest that activation of IL PV cells during social defeat predicts the development stress vulnerability in males, whereas activation of IL neurons is associated with a proactive response to social defeat exposure in females. Understanding how social dominance generates plasticity in IL PV cells should improve our understanding of the mechanisms by which behavioral treatments prior to stress might promote stress resilience.

Indexed as

AnxietyParvalbumin cellsRobust activity markerSocial defeatSocial dominanceStress resilienceVentral medial prefrontal cortex

Identifiers

PMID40230624
PMCPMC11994976

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.