Evidence mapPaperPMID 41880282Full record

ArticlePloS one2026

Impact of blast exposure on visual pathway: Mechanism exploration and novel diagnostic perspectives.

Yue Wang, Nan Yang, Xiaofan Chen, Xing Chen, Yalei Ning, Rongdi Yuan

Abstract read
In one paragraph

Article in PloS one, 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

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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

6 authors.

Yue WangDepartment of Ophthalmology, the Second Affiliated Hospital of Army Medical University, Chongqing, China.
Nan YangDepartment of Army Occupational Disease, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital of Army Medical University, Chongqing, China.
Xiaofan ChenDepartment of Ophthalmology, the Second Affiliated Hospital of Army Medical University, Chongqing, China.
Xing ChenDepartment of Army Occupational Disease, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital of Army Medical University, Chongqing, China.
Yalei NingDepartment of Army Occupational Disease, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital of Army Medical University, Chongqing, China.
Rongdi YuanDepartment of Ophthalmology, the Second Affiliated Hospital of Army Medical University, Chongqing, China.ORCID https://orcid.org/0009-0002-6226-4178

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blast-induced traumatic brain injury (bTBI), frequently observed in modern warfare, often presents without overt clinical symptoms initially, yet can involve visual impairment. However, the underlying mechanisms and long-term outcomes of visual dysfunction following blast exposure (BE) remain poorly understood. This study aimed to investigate the potential delayed effects of BE on visual function. A bTBI mouse model was established using a biological shock tube. Neurological deficits were assessed via the modified neurological severity score, while visual function was evaluated at multiple time points using flash visual evoked potentials (F-VEP) and a light-dark shuttle box. Ultrastructural evidence of damage was obtained through transmission electron microscopy (TEM). Inflammatory and pyroptosis markers were localized and quantified via immunofluorescence staining and Western blotting. Neuronal damage was detected by the terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining combined with neuron-specific nuclear protein (NeuN) immunofluorescence labeling. To assess therapeutic potential, MCC950 was administered to bTBI mice, and visual function was re-evaluated. The results demonstrated that visual dysfunction emerged at 24 hours post BE, followed by a transient recovery, and reappeared at 28 days post BE. Early demyelination of the optic nerve and later pyroptosis of neurons in the visual cortex were identified as key pathological features. MCC950 treatment effectively mitigated neuroinflammation and neuronal pyroptosis, thereby ameliorating late-phase visual dysfunction. These findings collectively suggest that BE leads to biphasic visual dysfunction, driven by distinct mechanisms at different stages. Early intervention targeting nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome activation may represent a promising therapeutic strategy to prevent late-phase visual impairment. Moreover, non-invasive F-VEP provides a sensitive and practical approach for assessing visual injury in bTBI.

Indexed as

Blast InjuriesBrain Injuries, TraumaticVisual PathwaysAnimalsDisease Models, AnimalEvoked Potentials, VisualMaleMiceMice, Inbred C57BLNeurons

Identifiers

PMID41880282
PMCPMC13016288

What Socratic 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 Socratic graph.