Evidence map›Paper›PMID 40580267›Full record

ArticleMolecular neurobiology2025

Phenserine Mitigates Neuroinflammation, Apoptosis, and Behavioural Deficits to Enhance Motor Function and Recovery in a Mouse Model of Spinal Cord Injury.

Lahanya Guha, Divya Goyal, Nidhi Singh, Mamidi Teena, Inbo Han, Hemant Kumar

Abstract read
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Article in Molecular neurobiology, 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

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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

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.

Lahanya GuhaDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Opposite Air Force Station, Palaj, P.O. - 382355, Gandhinagar, Gujarat, India.
Divya GoyalDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Opposite Air Force Station, Palaj, P.O. - 382355, Gandhinagar, Gujarat, India.
Nidhi SinghDepartment of Biotechnology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, India.
Mamidi TeenaDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Opposite Air Force Station, Palaj, P.O. - 382355, Gandhinagar, Gujarat, India.
Inbo HanDepartment of Neurosurgery, CHA University School of Medicine, CHA Bundang Medical Centre, 59 Yatapro, Bundangu, Seongnam-Si, Gyeonggi-Do, South Korea. hanib@cha.ac.kr.
Hemant KumarDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Opposite Air Force Station, Palaj, P.O. - 382355, Gandhinagar, Gujarat, India. hemant@niperahm.res.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal cord injury is a debilitating medical condition that results in paralysis and loss of sensorimotor function below the level of injury. The pathological cascade following the injury involves inflammation, apoptosis, blood-spinal cord barrier integrity disruption, axonal damage, glial scarring, and demyelination. This study evaluates the therapeutic potential of phenserine, a lipophilic phenyl carbamate derivative with neuroprotective, anti-inflammatory, and anti-apoptotic properties, in a compression-induced spinal cord injury model in C57bl/6 mice. Intraperitoneal administration of phenserine (5 mg/kg, twice daily for 5 days) significantly reduced inflammatory responses and blood-spinal cord barrier permeability at 1 day post-injury. By 7 days, it attenuated apoptotic signalling, and by 28 days, it reduced glial scarring and enhanced markers of axonal integrity and myelination. Neurobehavioral assessments further indicated that phenserine treatment improved motor and functional recovery outcomes. Collectively, our findings highlight phenserine as a promising therapeutic candidate that targets multiple secondary injury mechanisms to promote neuroprotection and functional restoration following spinal cord injury, marking a novel approach in managing traumatic spinal cord injury.

Indexed as

ApoptosisBehavior, AnimalMotor ActivityNeuroinflammatory DiseasesRecovery of FunctionSpinal Cord InjuriesAnimalsDisease Models, AnimalInflammationMaleMiceMice, Inbred C57BLNeuroprotective AgentsPhysostigmineSpinal CordNeuroprotective AgentsphenserinePhysostigmineApoptosisBlood spinal cord barrierInflammationPhenserineSpinal cord injury

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

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.