Evidence map›Paper›PMID 42691270›Full record

ArticleBehavioral neuroscience2026

Male mice are particularly vulnerable to cognitive impairment following mild traumatic brain injury.

James T Neal, Aimee Bertolli, Georgina M Aldridge, Eric B Emmons

Abstract read
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Article in Behavioral neuroscience, 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

5 · Who and what money

Authors and funding

4 authors.

James T NealDepartment of Psychology and Neuroscience, Drake University.ORCID 0009-0002-4468-745X
Aimee BertolliDepartment of Neurology, Carver College of Medicine, University of Iowa.ORCID 0009-0005-0595-1125
Georgina M AldridgeDepartment of Psychology and Neuroscience, Drake University.ORCID 0000-0002-8025-1189
Eric B EmmonsDepartment of Psychology and Neuroscience, Drake University.ORCID 0000-0001-5351-5073

Funding

Vulnerability of the ascending arousal network to alpha-synuclein pathologyRF1NS134833 · NINDS · UNIVERSITY OF IOWA · PI ALDRIDGE, GEORGINA · 2024 to 2024
$2.2M
NIH HHSNINDS NIH HHSNINDS NIH HHS RF1 NS134833
6 · The paper itself

Abstract

Traumatic brain injuries (TBIs) result from impact to or rapid displacement of the brain and can lead to various neurological deficits involving working memory, decision making, and anxiety. While large-scale effects of brain damage are well-described for more severe TBIs, less is known about the extent and duration of cognitive deficits at the mild level. Interval timing can provide a helpful window into cognition in mice and humans. Interval-timing behavior is impaired in a wide range of neuropsychiatric disease states, but less is known about whether it is impaired by mild TBI (mTBI). Furthermore, novel object recognition and the Barnes maze tests are valuable assays for evaluating spatial learning, working memory, and anxietylike behavior in mice. Here, we employed a weight-drop model of mTBI to investigate cognitive and behavioral changes resulting from mTBI treatment. mTBI mice were not consistently impaired in either interval timing or novel object recognition, but they demonstrated impaired spatial memory in the Barnes maze. Interestingly, between-sex comparisons revealed impairments in male mTBI mice in the interval-timing task, suggesting that male and female mice may be differently affected by mTBIs. (PsycInfo Database Record (c) 2026 APA, all rights reserved).

Identifiers

PMID42691270

What OpenQuestion holds

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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.