Evidence map›Paper›PMID 39106086›Full record

ArticleUnited European gastroenterology journal2024

Translational evaluation of Gelsectan

Orsolya Inczefi, Hélène Eutamene, Fanny Placide, Valérie Tondereau, Petra Pallagi, Mária Bagyánszki, Nikolett Bódi, Nikolett Gémes, Gábor Szebeni, Tamás Molnár and 2 more

Abstract read
In one paragraph

Article in United European gastroenterology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Viable and Heat-InactivatedMicroorganisms · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Translational evaluation of GelsectanUnited European gastroenterology journal · 2024
    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

12 authors.

Orsolya InczefiDepartment of Medicine, Centre for Gastroenterology, University of Szeged, Szeged, Hungary.ORCID 0000-0001-7974-1263
Hélène EutameneUMR 1331, Toxalim (Research Centre in Food Toxicology), INRAE, Université de Toulouse III, ENVT, Toulouse, France.
Fanny PlacideUMR 1331, Toxalim (Research Centre in Food Toxicology), INRAE, Université de Toulouse III, ENVT, Toulouse, France.
Valérie TondereauUMR 1331, Toxalim (Research Centre in Food Toxicology), INRAE, Université de Toulouse III, ENVT, Toulouse, France.
Petra PallagiDepartment of Medicine, Centre for Gastroenterology, University of Szeged, Szeged, Hungary.
Mária BagyánszkiDepartment of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
Nikolett BódiDepartment of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
Nikolett GémesLaboratory of Functional Genomics, HUN-REN Biological Research Centre, Szeged, Hungary.
Gábor SzebeniLaboratory of Functional Genomics, HUN-REN Biological Research Centre, Szeged, Hungary.
Tamás MolnárDepartment of Medicine, Centre for Gastroenterology, University of Szeged, Szeged, Hungary.ORCID 0000-0003-0599-182X
Vassilia TheodorouUMR 1331, Toxalim (Research Centre in Food Toxicology), INRAE, Université de Toulouse III, ENVT, Toulouse, France.
Richárd RókaDepartment of Medicine, Centre for Gastroenterology, University of Szeged, Szeged, Hungary.

Funding

Devintec SAGLHungarian National Research, Development and Innovation Office 116370
6 · The paper itself

Abstract

backgroundGelsectan

methodsAnimals: Wistar rats received gavage with XOS, XG + PPGS or XG + PPGS + XOS, as a single dose or for 7 days before a partial restraint stress (PRS). Visceromotor response to rectal distension and total gut paracellular permeability to

resultsAnimal studies: In control rats, PRS significantly increased visceromotor response as well as gut paracellular permeability. Single dose administration of XG + PPGS + XOS failed to reverse PRS, but 7 days of oral treatment reversed PRS-induced rectal hypersensitivity and gut hyperpermeability. Human studies: Gelsectan

conclusionsGelsectan

Indexed as

DiarrheaDisease Models, AnimalGlucansIntestinal MucosaIrritable Bowel SyndromePermeabilityRats, WistarXylansAbdominal PainAdultAnimalsFemaleHumansMaleMiddle AgedOligosaccharidesGlucansOligosaccharidesXylansxyloglucanGelsectangut hyperpermeabilityirritable bowel syndromerectal hypersensitivity

Identifiers

PMID39106086
PMCPMC11485395

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.