Evidence map›Paper›PMID 41577806›Full record

ArticleScientific reports2026

Development of a paediatric model of diffuse traumatic brain injury in ferrets.

Justin L Krieg, Carl Hooper, Hasini Kapuwelle, Rebecca P George, Rebecca J Hood, William T O'Brien, Stuart J McDonald, Anna V Leonard, Renée J Turner, Frances Corrigan

Abstract read
In one paragraph

Article in Scientific reports, 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

10 authors.

Justin L KriegTranslational Neuropathology Laboratory, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, Australia.
Carl HooperTranslational Neuropathology Laboratory, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, Australia.
Hasini KapuwelleTranslational Neuropathology Laboratory, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, Australia.
Rebecca P GeorgeTranslational Neuropathology Laboratory, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, Australia.
Rebecca J HoodTranslational Neuropathology Laboratory, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, Australia.
William T O'BrienDepartment of Neuroscience, School of Translational Medicine, Monash University, 99 Commercial Road, Melbourne, VIC, Australia.
Stuart J McDonaldDepartment of Neuroscience, School of Translational Medicine, Monash University, 99 Commercial Road, Melbourne, VIC, Australia.
Anna V LeonardTranslational Neuropathology Laboratory, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, Australia.
Renée J TurnerTranslational Neuropathology Laboratory, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, Australia.
Frances CorriganTranslational Neuropathology Laboratory, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, Australia. frances.corrigan@adelaide.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a leading cause of death and disability in children, especially those under five, with younger children more vulnerable to persistent cognitive and neuropsychological effects due to disrupted brain development. Paediatric brains are biomechanically more susceptible to diffuse axonal injury due to anatomical differences, with axonal injury observed in up to 80% of hospitalized children. Despite this, many preclinical TBI models focus on focal injuries, whereas to better model the evolution of axonal injury in the paediatric brain, clinically-relevant diffuse pre-clinical models are required. In this study gyrencephalic paediatric ferrets (2–3 months) equivalent to a 3–5-year-old child were injured with the Closed Head Impact Model of Engineered Rotational Acceleration (CHIMERA), and the axonal injury response and resultant motor and cognitive deficits examined to 72 h post-injury. Injury was associated with extensive axonal injury, as detected via both the amyloid precursor protein (APP) for transport disruption and neurofilament light (NFL) for neurofilament integrity, in key structures including the corpus callosum, fornix and cortical white matter. Serum GFAP was increased within 30 min of injury, returning to baseline by 72 h, with NFL elevated from 24 h to 72 h post-injury. Injured ferrets had deficits in balance, working memory and spatial memory. The adaptation of the CHIMERA model to paediatric ferrets provides the opportunity to investigate factors driving axonal pathology post-injury and how these interact with neurodevelopment.

Indexed as

Brain Injuries, TraumaticDisease Models, AnimalAmyloid beta-Protein PrecursorAnimalsAxonsFemaleFerretsGlial Fibrillary Acidic ProteinMaleAmyloid beta-Protein PrecursorGlial Fibrillary Acidic ProteinAxonal injuryCognitionDiffuse traumatic brain injuryFerretMotorPaediatric

Identifiers

PMID41577806
PMCPMC12901044

What Socratic holds

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LicenceCC BY
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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.