Evidence map›Paper›PMID 40745687›Full record

ArticleStress (Amsterdam, Netherlands)2025

Profiling of research domain criteria-based behaviors following single prolonged stress in male C57BL/6J mice.

Krysten P O'Hara, Savanna M King, Rachel D Penrod, Jennifer A Rinker, Patrick J Mulholland

Abstract read
In one paragraph

Article in Stress (Amsterdam, Netherlands), 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

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

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

5 authors.

Krysten P O'HaraDepartment of Neuroscience, Medical University of South Carolina, Charleston, South Carolina, USA.
Savanna M KingDepartment of Neuroscience, Medical University of South Carolina, Charleston, South Carolina, USA.
Rachel D PenrodDepartment of Neuroscience, Medical University of South Carolina, Charleston, South Carolina, USA.
Jennifer A RinkerDepartment of Neuroscience, Medical University of South Carolina, Charleston, South Carolina, USA.
Patrick J MulhollandDepartment of Neuroscience, Medical University of South Carolina, Charleston, South Carolina, USA.

Funding

TREATING ETHANOL WITHDRAWAL WITH LORAZEPAM/NALTREXONEP50AA010761 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Patrick J. Mulholland · 1996 to 2026
$46.8M
Kv7 channels and heavy alcohol drinkingR01AA023288 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MULHOLLAND, PATRICK J. · 2014 to 2023
$3.4M
Stress and Ethanol Dependence: SK Channels and GlutamateU01AA020930 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MULHOLLAND, PATRICK J. · 2012 to 2021
$2.6M
NIAAA NIH HHS P50 AA010761NIAAA NIH HHS R01 AA023288NIAAA NIH HHS U01 AA020930
6 · The paper itself

Abstract

Post-traumatic stress disorder (PTSD) affects approximately one in 11 people throughout their lifetime yet current treatment options, such as behavioral therapies or pharmaceuticals, suffer from low medical adherence and often fail to fully address all the symptoms. Therefore, it is necessary to better understand maladaptive behaviors in PTSD to guide new treatments. Single-prolonged stress (SPS) is a rodent model of stress that parallels certain human neurophysiological and neurobehavioral changes occurring in PTSD. SPS is a single-day sequential stressor exposure-restraint stress, group forced swim, predator odor exposure, and isoflurane until loss of consciousness-followed by 7 days of stress incubation. Here, we investigated multiple cohorts of male C57BL/6J mice early after SPS and stress incubation (8-10 days) on behavioral tasks (elevated plus maze (EPM), three-chamber sociability, cost-benefit conflict (CBC), home cage behavior, scent avoidance and defensive burying tasks) that test multiple PTSD-related symptoms. Behavioral assessment included efforts to replicate published findings (i.e., EPM) and introducing newer tasks (i.e., CBC) that have not yet been tested in the SPS mouse model. While most of these tasks and standardized metrics failed to capture behavioral differences in SPS-treated male C57BL/6J mice, we did observe deficits in social novelty preference in the stressed mice. These studies add to a growing literature on inconsistencies in behavioral outcomes produced by the mouse SPS paradigm that could be potentially explained by mouse strain or procedural differences. Overall, this study demonstrated that behavior in male C57BL/6J mice were not affected after SPS apart from social novelty preference.

Indexed as

Behavior, AnimalStress Disorders, Post-TraumaticStress, PsychologicalAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLSocial BehavioranxietybehaviorC57BL/6J micePost-traumatic stress disorderRDoCsingle-prolonged stress

Identifiers

PMID40745687
PMCPMC12989816

What Socratic 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 Socratic graph.