Evidence map›Paper›PMID 40597179›Full record

ArticleMolecular brain2025

Systemic semaglutide provides a mild vasoprotective and antineuroinflammatory effect in a rat model of ocular hypertensive glaucoma.

Zaynab A Mouhammad, Anne Rombaut, Mariana Yolotzin García Bermúdez, Rupali Vohra, James R Tribble, Pete A Williams, Miriam Kolko

Abstract read
In one paragraph

Article in Molecular brain, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
–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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Review
  7. 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

7 authors.

Zaynab A MouhammadDepartment of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, Copenhagen, 2100 CPH, Denmark.
Anne RombautDepartment of Clinical Neuroscience, Division of Eye and Vision, St. Erik Eye Hospital, Karolinska Institutet, Stockholm, Sweden.
Mariana Yolotzin García BermúdezDepartment of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, Copenhagen, 2100 CPH, Denmark.
Rupali VohraDepartment of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, Copenhagen, 2100 CPH, Denmark.
James R TribbleDepartment of Clinical Neuroscience, Division of Eye and Vision, St. Erik Eye Hospital, Karolinska Institutet, Stockholm, Sweden.
Pete A Williams *Department of Clinical Neuroscience, Division of Eye and Vision, St. Erik Eye Hospital, Karolinska Institutet, Stockholm, Sweden. pete.williams@ki.se.
Miriam Kolko *Department of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, Copenhagen, 2100 CPH, Denmark. miriamk@sund.ku.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glaucoma is a neurodegenerative disease affecting retinal ganglion cells (RGCs), with a multifactorial genesis that includes inflammation and vascular dysfunction. Emerging evidence suggests that glucagon-like peptide 1 receptor agonist (GLP-1RAs) may serve as promising neuroprotective agents in glaucoma. In this study, we investigated the neuroprotective potential of the GLP-1RA semaglutide (SEM) in a rat model of ocular hypertension (OHT) induced by paramagnetic bead injections in Brown Norwegian rats. Rats were divided into four cohorts, two normotensive (NT) cohorts, and two OHT cohorts, treated with either SEM or saline (HBSS), which served as control. Systemic SEM or HBSS administration was initiated simultaneously with OHT induction. We observed that SEM administration seemed to delay the increase in intraocular pressure (IOP) associated with OHT. Although SEM administration did not improve RGC survival, it significantly improved astrocytic fractal dimension value and lacunarity. In conclusion, our findings suggest that GLP-1RAs may exert neuroprotective effects by delaying IOP elevation and preventing OHT-induced reactive astrocyte and vascular remodeling. These findings highlight the potential of GLP-1RAs for retinal neuroprotection, but further studies are needed to elucidate their applicability in glaucoma.

Indexed as

Anti-Inflammatory AgentsGlaucomaGlucagon-Like PeptidesNeuroprotective AgentsOcular HypertensionAnimalsAstrocytesCell SurvivalDisease Models, AnimalGlucagon-Like Peptide 1InflammationIntraocular PressureMaleRatsRats, Inbred BNRetinal Ganglion CellsAnti-Inflammatory AgentsGlucagon-Like Peptide 1Glucagon-Like PeptidesNeuroprotective AgentsSemaglutideAstrocytesGlaucomaGLP-1 receptor agonistsNeurodegenerationNeuroinflammationNeuroprotectionRetinaRetinal ganglion cellSemaglutide

Identifiers

PMID40597179
PMCPMC12211916

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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.