Evidence map›Paper›PMID 41462062›Full record

ArticleScientific reports2025

Effects of acute biperiden treatment following traumatic brain injury in male rats.

Matheus B Braga, Viviam Sanabria, Simone Romariz, Christiane Gimenes, Michele Longoni Calió, Maira L Foresti, Luiz Eugênio Mello, Beatriz M Longo

Abstract read
In one paragraph

Article in Scientific reports, 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

8 authors.

Matheus B BragaLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Viviam SanabriaLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Simone RomarizLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Christiane GimenesLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Michele Longoni CalióLaboratory of Neurobiology, Department of Physiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Maira L ForestiLaboratory of Neurobiology, Department of Physiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Luiz Eugênio MelloLaboratory of Neurobiology, Department of Physiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Beatriz M LongoLaboratory of Neurophysiology, Department of Physiology, Universidade Federal de São Paulo, São Paulo, Brazil. beatriz.longo@unifesp.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 311619/2019-3Conselho Nacional de Desenvolvimento Científico e Tecnológico 312904/2021-5Coordenação de Aperfeiçoamento de Pessoal de Nível Superior CAPES; Finance Code 001Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/24561-5Fundação de Amparo à Pesquisa do Estado de São Paulo 2022/00249-8
6 · The paper itself

Abstract

Traumatic brain injury (TBI) remains a leading cause of morbidity and mortality, with no effective treatments available. Biperiden, a muscarinic receptor antagonist, has demonstrated beneficial effects by modulating neural plasticity and reducing excitotoxicity. This study investigated the acute impact of cellular and structural changes in a moderate TBI model using lateral fluid percussion injury (LFPI) in male Wistar rats. Biperiden (8 mg/kg) was administered intraperitoneally at 6 h post-injury, followed by two additional doses at 8-hour intervals. Brain and blood were collected twenty-four hours after TBI for, histological, immunohistochemical, and Single Molecule Array (SIMOA) analyses. Results revealed that biperiden-treated (TBI-BIP) rats exhibited diminished degenerating neurons, lower T-tau and NfL levels, decreased astrocyte activation, and restored microglia morphology compared to saline-treated (TBI-SAL) rats, attenuating TBI-induced damage. Motor deficits were most pronounced on Day 1 post-trauma, with non-significant statistical difference in neuroscore performance between the TBI groups, however the biperiden treatment modulates astrocyte reactivity, diminish gliosis, and promote a neuroprotective phenotype. Additionally, biperiden preserves microglial branching following injury. These findings demonstrate that biperiden exerts beneficial effects during the acute phase of TBI by decreasing neuronal degeneration, excitotoxicity, and inflammation, highlighting its therapeutic potential for post-TBI intervention.

Indexed as

Brain Injuries, TraumaticMuscarinic AntagonistsNeuroprotective AgentsAnimalsAstrocytesBrainDisease Models, AnimalMaleMicrogliaNeuronsRatsRats, WistarMuscarinic AntagonistsNeuroprotective AgentsAnticholinergicBiperidenGlial modulationInflammatoryLateral fluid percussion injury

Identifiers

PMID41462062
PMCPMC12748752

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.