Evidence map›Paper›PMID 40123100›Full record

ArticleAlcohol, clinical & experimental research2025

The impact of adolescent drinking on traumatic brain injury-induced cognitive deficits and alcohol preference in adult C57BL/6J mice.

Yunhui H Xu, Hannah G Sexton, Angela N Henderson-Redmond, Christian Harris, Jason D Huber, Mary-Louise Risher

Abstract read
In one paragraph

Article in Alcohol, clinical & experimental research, 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. Review
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

6 authors.

Yunhui H XuDepartment of Biomedical Research, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, USA.
Hannah G SextonDepartment of Biomedical Research, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, USA.
Angela N Henderson-RedmondDepartment of Biomedical Research, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, USA.
Christian HarrisDepartment of Biomedical Research, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, USA.
Jason D HuberDepartment of Pharmaceutical Sciences, West Virginia University, Health Sciences Center, Morgantown, West Virginia, USA.
Mary-Louise RisherDepartment of Biomedical Research, Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia, USA.ORCID 0000-0002-3139-4378

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Reagan Curtis · 2012 to 2026
$81.0M
mitoNEET as a therapeutic target for mitigating ischemic brain injury following MCAOR01NS129998 · NINDS · WEST VIRGINIA UNIVERSITY · PI Werner Geldenhuys, JASON D HUBER · 2023 to 2026
$2.1M
Biomedical Laboratory Research and Development, VA Office of Research and Development BX005403BLRD VA I01 BX005403National Institute of General Medical Sciences of the National Institutes of Health 2U54GM104942NIGMS NIH HHS U54 GM104942NINDS NIH HHS R01 NS129998
6 · The paper itself

Abstract

backgroundIndustrial workers and active military personnel within combat roles face heightened risk for blast pressure wave traumatic brain injury (bTBI). Previous studies have shown that experiencing TBI is associated with increased alcohol (EtOH) consumption and illicit substance use. Notably, alcohol use typically begins during late adolescence or early adulthood, a period that precedes many TBI incidents; moreover, early-onset drinking is further associated with heightened risk of developing an alcohol use disorder (AUD) even in the absence of TBI. Adolescent binge drinking can induce lasting cognitive and astrocyte changes, impacting brain recovery and repair. However, the impact of adolescent drinking history on behavioral recovery after bTBI and its role in the subsequent escalation of alcohol consumption remain unexplored. Here, we used a mouse model to investigate how adolescent (PND28-42) and young adult (PND60-90) EtOH consumption affects behavioral outcomes following bTBI. We aim to determine whether the history of adolescent binge drinking contributes to bTBI-induced escalation in EtOH intake, preference, or worsened fear memory and anxiety.

methodsAdolescent mice were subjected to drinking in the dark (DID) EtOH paradigm for 4 weeks, then randomly assigned to sham, mild-bTBI, or severe-bTBI. Behavioral testing was conducted, followed by a second DID.

resultsBoth EtOH and bTBI independently induced hyperlocomotor activity in a sex-dependent manner. These findings reflect an increase in risk-taking rather than generalized anxiety. Importantly, a history of adolescent EtOH consumption synergistically worsened bTBI-induced impaired fear extinction in both sexes. Changes in EtOH preference post-bTBI are context-dependent, with male mice showing a significant decrease in preference following mild-bTBI and prior EtOH exposure, while females exhibited a trend toward increased preference post-bTBI, with significant increases in preference observed only when comparing pre- to post-bTBI drinking behavior.

conclusionsBoth males and females exhibited vulnerability to the combined effects of adolescent EtOH consumption and bTBI on fear extinction, while female mice showed a unique vulnerability to the escalation in EtOH preference.

Indexed as

Alcohol DrinkingBrain Injuries, TraumaticCognitive DysfunctionUnderage DrinkingAnimalsAnxietyBinge DrinkingEthanolFearFemaleMaleMiceMice, Inbred C57BLEthanoladolescencealcoholbehaviorgliamicetraumatic brain injury

Identifiers

PMID40123100
PMCPMC12097944

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Registered trials

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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 OpenQuestion graph.