Evidence map›Paper›PMID 41284070›Full record

ArticlePsychopharmacology2026

Single prolonged stress in mice: interactions between alcohol drinking, negative affect, and fear learning.

Aditi B Buch, Ava L Shipman, Nicolas J Azzarello, Annie W Zhou, Samuel W Centanni

Abstract read
In one paragraph

Article in Psychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Aditi B Buch *Department of Translational Neuroscience, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC, NC 27103, USA.ORCID http://orcid.org/0000-0002-3593-7632
Ava L Shipman *Department of Translational Neuroscience, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC, NC 27103, USA.
Nicolas J AzzarelloDepartment of Translational Neuroscience, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC, NC 27103, USA.
Annie W ZhouDepartment of Translational Neuroscience, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC, NC 27103, USA.
Samuel W CentanniDepartment of Translational Neuroscience, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC, NC 27103, USA. Samuel.Centanni@wfusm.edu.ORCID http://orcid.org/0000-0002-3941-7677

Funding

Insula-BNST Circuit Regulation of AUDR01AA031477 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CENTANNI, SAMUEL · 2025 to 2025
$2.6M
Insular cortex-BNST neural circuit regulation of chronic alcohol abstinence-induced negative affectR00AA027774 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CENTANNI, SAMUEL · 2022 to 2024
$832k
Role of the BLA-Insula circuit in stress-induced aversive drinking and negative affective statesF31AA032178 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Aditi Buch · 2025 to 2026
$100k
NIAAA NIH HHS F31 AA032178NIAAA NIH HHS R00 AA027774NIAAA NIH HHS R01 AA031477
6 · The paper itself

Abstract

RATIONALE &

objectiveExposure to traumatic stressors can have detrimental effects on one's well-being. Alcohol is often used as a coping mechanism to alleviate stress, leading to the development of alcohol use disorder (AUD). Furthermore, sex dimorphisms in stress and AUD alter their progression and sustenance. To investigate these interactions for effective treatment strategies, validated and exhaustive preclinical models are necessary. Here, we designed a comprehensive study that examines how traumatic stress influences ethanol drinking patterns and PTSD-like phenotypes in male and female mice with Single Prolonged Stress (SPS).

methodsMale and female C57BL/6 J mice underwent SPS, a model of traumatic stress consisting of a series of consecutive stressors, followed by a 7-day stress incubation period. Mice then underwent a series of tests for aversive state, fear discrimination, and drinking patterns during continuous and limited ethanol access. RESULTS &

conclusionsSPS selectively increased negative affect and startle responses in male mice, while females were unaffected. SPS disrupted discrimination adjustment between fear and safety cues during extinction, while ethanol exposure attenuated overall fear responses. SPS maintained baseline sex differences in consumption. Furthermore, female consumption increased when access was provided prior to and continuously throughout SPS and fear conditioning, contrasting with groups exposed to ethanol afterwards. In summary, we identified a distinct sex specific relationship between traumatic stress, fear memory, and the timing of ethanol consumption. We highlight SPS as a robust translational model for exploring the sex-specific neurobiological mechanisms driving traumatic stress-induced affective disturbances.

Indexed as

AffectAlcohol DrinkingFearStress Disorders, Post-TraumaticStress, PsychologicalAnimalsDisease Models, AnimalEthanolExtinction, PsychologicalFemaleMaleMiceMice, Inbred C57BLReflex, StartleSex CharacteristicsSex FactorsEthanolAlcoholBinge-like consumptionFear conditioningNegative affectSex differencesSPSStartleStressVolitional drinking

Identifiers

PMID41284070
PMCPMC13242430

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.