» Articles » PMID: 20650926

The Mast Cell Stabiliser Ketotifen Decreases Visceral Hypersensitivity and Improves Intestinal Symptoms in Patients with Irritable Bowel Syndrome

Overview
Journal Gut
Specialty Gastroenterology
Date 2010 Jul 24
PMID 20650926
Citations 145
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Mast cell activation is thought to be involved in visceral hypersensitivity, one of the main characteristics of the irritable bowel syndrome (IBS). A study was therefore undertaken to investigate the effect of the mast cell stabiliser ketotifen on rectal sensitivity and symptoms in patients with IBS.

Methods: 60 patients with IBS underwent a barostat study to assess rectal sensitivity before and after 8 weeks of treatment. After the initial barostat, patients were randomised to receive ketotifen or placebo. IBS symptoms and health-related quality of life were scored. In addition, mast cells were quantified and spontaneous release of tryptase and histamine was determined in rectal biopsies and compared with biopsies from 22 age- and gender-matched healthy volunteers.

Results: Ketotifen but not placebo increased the threshold for discomfort in patients with IBS with visceral hypersensitivity. This effect was not observed in normosensitive patients with IBS. Ketotifen significantly decreased abdominal pain and other IBS symptoms and improved quality of life. The number of mast cells in rectal biopsies and spontaneous release of tryptase were lower in patients with IBS than in healthy volunteers. Spontaneous release of histamine was mostly undetectable but was slightly increased in patients with IBS compared with healthy volunteers. Histamine and tryptase release were not altered by ketotifen.

Conclusions: This study shows that ketotifen increases the threshold for discomfort in patients with IBS with visceral hypersensitivity, reduces IBS symptoms and improves health-related quality of life. Whether this effect is secondary to the mast cell stabilising properties of ketotifen or H(1) receptor antagonism remains to be further investigated. Trial Registration Number NTR39, ISRCTN22504486.

Citing Articles

Beyond the "Master" Role in Allergy: Insights into Intestinal Mast Cell Plasticity and Gastrointestinal Diseases.

Molfetta R, Carnevale A, Marangio C, Putro E, Paolini R Biomedicines. 2025; 13(2).

PMID: 40002733 PMC: 11853218. DOI: 10.3390/biomedicines13020320.


Rome Foundation Working Team Report on overlap in disorders of gut-brain interaction.

Barbara G, Aziz I, Ballou S, Chang L, Ford A, Fukudo S Nat Rev Gastroenterol Hepatol. 2025; .

PMID: 39870943 DOI: 10.1038/s41575-024-01033-9.


The Role of Gut Microbiome in Irritable Bowel Syndrome: Implications for Clinical Therapeutics.

Zhao Y, Zhu S, Dong Y, Xie T, Chai Z, Gao X Biomolecules. 2025; 14(12.

PMID: 39766350 PMC: 11674646. DOI: 10.3390/biom14121643.


Toll-like receptor 4 plays a vital role in irritable bowel syndrome: a scoping review.

Wan X, Wang L, Wang Z, Wan C Front Immunol. 2025; 15:1490653.

PMID: 39749341 PMC: 11693509. DOI: 10.3389/fimmu.2024.1490653.


The gut-brain axis and pain signalling mechanisms in the gastrointestinal tract.

Meerschaert K, Chiu I Nat Rev Gastroenterol Hepatol. 2024; 22(3):206-221.

PMID: 39578592 DOI: 10.1038/s41575-024-01017-9.