The ClC-2 Chloride Channel Activator, Lubiprostone, Improves Intestinal Barrier Function in Biopsies from Crohn’s Disease but Not Ulcerative Colitis Patients

Author:

Park Young Su12,Kang Sang Bum13ORCID,Marchelletta Ronald R.1,Penrose Harrison M.1,Ruiter-Visser Roos14,Jung Barbara1,Docherty Michael J.1,Boland Brigid S.1,Sandborn William J.1,McCole Declan F.5ORCID

Affiliation:

1. Division of Gastroenterology, School of Medicine, University of California San Diego, La Jolla, CA 92093, USA

2. Department of Internal Medicine, Division of Gastroenterology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea

3. Division of Gastroenterology, Department of Internal Medicine, St. Mary’s Hospital, Catholic University of Korea, Seoul 06591, Republic of Korea

4. Department of Internal Medicine, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands

5. Division of Biomedical Sciences, School of Medicine, University of California, Riverside, 307 SOM Research Building, 900 University Ave, Riverside, CA 92521, USA

Abstract

The prostone analog, lubiprostone, is approved to manage constipation-predominant irritable bowel syndrome. Lubiprostone also protects intestinal mucosal barrier function in animal models of colitis. The aim of this study was to determine if lubiprostone improves barrier properties in isolated colonic biopsies from Crohn’s disease (CD) and ulcerative colitis (UC) patients. Sigmoid colon biopsies from healthy subjects, CD and UC patients in remission, and CD patients with active disease were mounted in Ussing chambers. Tissues were treated with lubiprostone or vehicle to determine the effects on transepithelial electrical resistance (TER), FITC-dextran 4kD (FD4) permeability, and electrogenic ion transport responses to forskolin and carbachol. Localization of the tight junction protein, occludin, was determined by immunofluorescence. Lubiprostone significantly increased ion transport across control, CD and UC remission biopsies but not active CD. Lubiprostone selectively improved TER in both CD remission and active disease biopsies but not in control or UC biopsies. The improved TER was associated with increased membrane localization of occludin. Lubiprostone selectively improved barrier properties of biopsies from CD patients vs. UC and independent of an ion transport response. These data indicate that lubiprostone has potential efficacy in improving mucosal integrity in Crohn’s disease.

Funder

Takeda Pharmaceuticals North America Inc.

Crohn’s and Colitis Foundation Senior Research Award

Publisher

MDPI AG

Subject

Pharmaceutical Science

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