Evidence map›Paper›PMID 40159830›Full record

ArticleIntestinal research2025

Restoration of colonic barrier function by tofacitinib in experimental colitis: anti-inflammatory effects and decreased expression of claudins-2 and claudin-15.

Humberto Barbosa da Costa Filho, Gerardo Autran Cavalcante Araújo, Thiago Meneses Araújo Leite Sales, Suliana Mesquita Paula, Marco Antonio de Freitas Clementino, Alexandre Havt, Pedro Marcos Gomes Soares, Marcellus Henrique Loiola Ponte Souza

Abstract read
In one paragraph

Article in Intestinal research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

8 authors.

Humberto Barbosa da Costa FilhoDepartment of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza, Brazil.
Gerardo Autran Cavalcante AraújoDepartment of Medicine, School of Medicine, Federal University of Ceará, Fortaleza, Brazil.
Thiago Meneses Araújo Leite SalesDepartment of Medicine, School of Medicine, Federal University of Ceará, Fortaleza, Brazil.
Suliana Mesquita PaulaDepartment of Medicine, School of Medicine, Federal University of Ceará, Fortaleza, Brazil.
Marco Antonio de Freitas ClementinoDepartment of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza, Brazil.
Alexandre HavtDepartment of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza, Brazil.
Pedro Marcos Gomes SoaresDepartment of Morphology, Federal University of Ceará, Fortaleza, Brazil.
Marcellus Henrique Loiola Ponte SouzaDepartment of Medicine, School of Medicine, Federal University of Ceará, Fortaleza, Brazil.

Funding

Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico 05/2019
6 · The paper itself

Abstract

BACKGROUND/

aimsInflammatory bowel disease can be triggered by disturbances in intestinal mucosal integrity, leading to bacterial transmigration. The treatment of inflammatory bowel diseases must not only aim to reduce inflammation, but also to reverse the damage to mucosal barrier function. Janus kinase (JAK) inhibitors have been used to treat inflammatory diseases, including ulcerative colitis. However, little is known about the ability of this class of drugs to reverse the loss of mucosal integrity. This study evaluated the effects of tofacitinib, a JAK pathway inhibitor, on inflammation and colonic mucosal integrity in a rat model of 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis.

methodsColitis was induced in Wistar rats via rectal administration of TNBS (20 mg+50% ethanol). The control group received only saline. The animals were pretreated with tofacitinib (15 mg/kg) or saline 30 minutes before induction and twice daily thereafter. Seven days after induction, the animals were euthanized, the colon was removed, and myeloperoxidase activity, baseline transepithelial electrical resistance (TER), TER after 1 hour, and fluorescein permeability were assessed. Tight junction proteins in the colon (claudin-2, claudin-15, and tricellulin) were detected using Western blotting.

resultsTofacitinib treatment significantly reduced (P< 0.05) the inflammatory parameters and preserved the integrity of the intestinal epithelial barrier compared with the colitis group (P< 0.05), increased baseline TER, reduced the drop in TER after 1 hour, and decreased paracellular permeability to fluorescein by reducing claudin-2 and claudin-15 expression.

conclusionsJAK inhibition by tofacitinib restored colonic barrier function through antiinflammatory effects and decreased claudin-2 and claudin-15 expressions.

Indexed as

Claudin-15Claudin-2ColitisMucosal barrier function

Identifiers

PMID40159830
PMCPMC12590074

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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.