Evidence map›Paper›PMID 36944922›Full record

ArticleBMC gastroenterology2023

Glepaglutide, a novel glucagon-like peptide-2 agonist, has anti-inflammatory and mucosal regenerative effects in an experimental model of inflammatory bowel disease in rats.

Jolanta Skarbaliene, Jesper Mosolff Mathiesen, Bjarne Due Larsen, Christian Thorkildsen, Yvette Miata Petersen

Open access · goldFull text read
In one paragraph

Article in BMC gastroenterology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Building and regenerating intestines by manipulating intestinal stem cells.Nature reviews. Gastroenterology & hepatology · 2026
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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

5 authors at 2 institutions in 2 countries.

Jolanta SkarbalieneResearch and Development, Zealand Pharma A/S, Sydmarken 11, 2860, Søborg, Denmark.ORCID http://orcid.org/0000-0003-3965-7504
Jesper Mosolff MathiesenResearch and Development, Zealand Pharma A/S, Sydmarken 11, 2860, Søborg, Denmark. jmmathiesen@zealandpharma.com.ORCID http://orcid.org/0000-0003-4251-4416
Bjarne Due LarsenResearch and Development, Zealand Pharma A/S, Sydmarken 11, 2860, Søborg, Denmark.ORCID http://orcid.org/0000-0001-6769-4682
Christian ThorkildsenResearch and Development, Zealand Pharma A/S, Sydmarken 11, 2860, Søborg, Denmark.ORCID http://orcid.org/0000-0001-9450-6675
Yvette Miata PetersenResearch and Development, Zealand Pharma A/S, Sydmarken 11, 2860, Søborg, Denmark.ORCID http://orcid.org/0000-0002-1643-2137
Zealand Pharma (Denmark) · DKRoche (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlucagon-like peptide-2 (GLP-2) enhances intestinal repair and attenuates inflammation in preclinical inflammatory bowel disease (IBD) models, making GLP-2 analogues attractive candidates for IBD therapy. Glepaglutide is a long-acting GLP-2 receptor agonist in clinical development for treatment of short bowel syndrome. Here, we investigated if glepaglutide is therapeutically beneficial in rats with small intestinal inflammation.

methodsSmall intestinal inflammation was induced with indomethacin in naive Wistar rats, followed by glepaglutide administration at different disease stages. Glepaglutide was administered in co-treatment and post-treatment regimens. Small intestinal length and concentrations of inflammatory markers α-1-acid glycoprotein and myeloperoxidase were used to assess anti-inflammatory effects. Small intestinal mass was evaluated to determine intestinotrophic effects.

resultsGlepaglutide co- and post-treatment significantly reduced severity of small intestinal inflammation, evidenced by reversed small intestinal shortening and decreased α-1-acid glycoprotein and/or myeloperoxidase concentration(s). Co- and post-treatment with glepaglutide also significantly increased small intestinal mass, indicating intestinal regenerative effects. Similar effects were observed in naive rats after glepaglutide treatment.

conclusionGlepaglutide has anti-inflammatory and intestinotrophic effects without the need for pre-treatment in a rat model of small intestinal inflammation. Thus, glepaglutide is of potential clinical interest for patients with IBD.

Indexed as

Glucagon-Like Peptide 2Inflammatory Bowel DiseasesAnimalsAnti-Inflammatory AgentsGlycoproteinsInflammationIntestinal MucosaModels, TheoreticalPeroxidaseRatsRats, WistarAnti-Inflammatory AgentsGlucagon-Like Peptide 2GlycoproteinsPeroxidaseAnti-inflammatoryGlepaglutideGLP-2Inflammatory bowel diseaseMucosal healing

Identifiers

PMID36944922
PMCPMC10029296
OpenAlexW4353016432

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read32
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 OpenQuestion graph.