The ClC-2 Chloride Channel Activator, Lubiprostone, Improves Intestinal Barrier Function in Biopsies from Crohn’s Disease but Not Ulcerative Colitis Patients
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 colon...
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Published in | Pharmaceutics Vol. 15; no. 3; p. 811 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.03.2023
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ISSN | 1999-4923 1999-4923 |
DOI | 10.3390/pharmaceutics15030811 |
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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. |
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AbstractList | 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. 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.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. |
Audience | Academic |
Author | Docherty, Michael J. McCole, Declan F. Marchelletta, Ronald R. Boland, Brigid S. Ruiter-Visser, Roos Sandborn, William J. Kang, Sang Bum Jung, Barbara Penrose, Harrison M. Park, Young Su |
AuthorAffiliation | 4 Department of Internal Medicine, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands 3 Division of Gastroenterology, Department of Internal Medicine, St. Mary’s Hospital, Catholic University of Korea, Seoul 06591, Republic of Korea 2 Department of Internal Medicine, Division of Gastroenterology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea 1 Division of Gastroenterology, School of Medicine, University of California San Diego, La Jolla, CA 92093, USA 5 Division of Biomedical Sciences, School of Medicine, University of California, Riverside, 307 SOM Research Building, 900 University Ave, Riverside, CA 92521, USA |
AuthorAffiliation_xml | – name: 1 Division of Gastroenterology, School of Medicine, University of California San Diego, La Jolla, CA 92093, USA – name: 2 Department of Internal Medicine, Division of Gastroenterology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea – name: 4 Department of Internal Medicine, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands – name: 5 Division of Biomedical Sciences, School of Medicine, University of California, Riverside, 307 SOM Research Building, 900 University Ave, Riverside, CA 92521, USA – name: 3 Division of Gastroenterology, Department of Internal Medicine, St. Mary’s Hospital, Catholic University of Korea, Seoul 06591, Republic of Korea |
Author_xml | – sequence: 1 givenname: Young Su surname: Park fullname: Park, Young Su – sequence: 2 givenname: Sang Bum orcidid: 0000-0002-1946-7896 surname: Kang fullname: Kang, Sang Bum – sequence: 3 givenname: Ronald R. surname: Marchelletta fullname: Marchelletta, Ronald R. – sequence: 4 givenname: Harrison M. surname: Penrose fullname: Penrose, Harrison M. – sequence: 5 givenname: Roos surname: Ruiter-Visser fullname: Ruiter-Visser, Roos – sequence: 6 givenname: Barbara surname: Jung fullname: Jung, Barbara – sequence: 7 givenname: Michael J. surname: Docherty fullname: Docherty, Michael J. – sequence: 8 givenname: Brigid S. surname: Boland fullname: Boland, Brigid S. – sequence: 9 givenname: William J. surname: Sandborn fullname: Sandborn, William J. – sequence: 10 givenname: Declan F. orcidid: 0000-0002-6286-0802 surname: McCole fullname: McCole, Declan F. |
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CitedBy_id | crossref_primary_10_3390_pharmaceutics16010029 crossref_primary_10_1007_s11010_025_05243_w crossref_primary_10_3390_gidisord7010011 crossref_primary_10_1136_gutjnl_2023_331579 crossref_primary_10_3390_nu17061064 crossref_primary_10_7759_cureus_63775 crossref_primary_10_1016_j_trechm_2024_10_005 |
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Keywords | occludin permeability epithelial chloride secretion ion transport inflammatory bowel disease tight junction |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Current position: Prometheus Biosciences, 3050 Science Park Road, San Diego, CA 92121, USA. Current position: Department of Psychiatry, Amsterdam UMC, VU University Medical Center (VUMC), 1081 HZ Amsterdam, The Netherlands. These authors contributed equally to the work. Current position: Department of Medicine, University of Washington, Seattle, WA 98195-6420, USA. |
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SubjectTerms | Biopsy Chloride chloride secretion Constipation Crohn's disease Cystic fibrosis Dosage and administration Drug therapy epithelial Fatty acids Inflammatory bowel disease ion transport Ions Irritable bowel syndrome Localization Lubiprostone occludin Patients Permeability Proteins Remission (Medicine) Testing Ulcerative colitis |
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Title | The ClC-2 Chloride Channel Activator, Lubiprostone, Improves Intestinal Barrier Function in Biopsies from Crohn’s Disease but Not Ulcerative Colitis Patients |
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