iNOS-dependent increase in colonic mucus thickness in DSS-colitic rats.

AIM: To investigate colonic mucus thickness in vivo in health and during experimental inflammatory bowel disease. METHODS: Colitis was induced with 5% DSS in drinking water for 8 days prior to experiment, when the descending colonic mucosa of anesthetized rats was studied using intravital microscopy...

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Main Authors: Olof Schreiber, Joel Petersson, Tomas Waldén, David Ahl, Stellan Sandler, Mia Phillipson, Lena Holm
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3747056?pdf=render
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spelling doaj-0ccbbdfbe0f94d18b9b39b705e80780a2020-11-24T21:12:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e7184310.1371/journal.pone.0071843iNOS-dependent increase in colonic mucus thickness in DSS-colitic rats.Olof SchreiberJoel PeterssonTomas WaldénDavid AhlStellan SandlerMia PhillipsonLena HolmAIM: To investigate colonic mucus thickness in vivo in health and during experimental inflammatory bowel disease. METHODS: Colitis was induced with 5% DSS in drinking water for 8 days prior to experiment, when the descending colonic mucosa of anesthetized rats was studied using intravital microscopy. Mucus thickness was measured with micropipettes attached to a micromanipulator. To assess the contributions of NOS and prostaglandins in the regulation of colonic mucus thickness, the non-selective NOS-inhibitor L-NNA (10 mg/kg bolus followed by 3 mg/kg/h), the selective iNOS-inhibitor L-NIL (10 mg/kg bolus followed by 3 mg/kg/h) and the non-selective COX-inhibitor diclofenac (5 mg/kg) were administered intravenously prior to experiment. To further investigate the role of iNOS in the regulation of colonic mucus thickness, iNOS -/- mice were used. RESULTS: Colitic rats had a thicker firmly adherent mucus layer following 8 days of DSS treatment than untreated rats (88±2 µm vs 76±1 µm). During induction of colitis, the thickness of the colonic mucus layer initially decreased but was from day 3 significantly thicker than in untreated rats. Diclofenac reduced the mucus thickness similarly in colitic and untreated rats (-16±5 µm vs -14±2 µm). While L-NNA had no effect on colonic mucus thickness in DSS or untreated controls (+3±2 µm vs +3±1 µm), L-NIL reduced the mucus thickness significantly more in colitic rats than in controls (-33±4 µm vs -10±3 µm). The importance of iNOS in regulating the colonic mucus thickness was confirmed in iNOS-/- mice, which had thinner colonic mucus than wild-type mice (35±3 µm vs 50±2 µm, respectively). Furthermore, immunohistochemistry revealed increased levels of iNOS in the colonic surface epithelium following DSS treatment. CONCLUSION: Both prostaglandins and nitric oxide regulate basal colonic mucus thickness. During onset of colitis, the thickness of the mucus layer is initially reduced followed by an iNOS mediated increase.http://europepmc.org/articles/PMC3747056?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Olof Schreiber
Joel Petersson
Tomas Waldén
David Ahl
Stellan Sandler
Mia Phillipson
Lena Holm
spellingShingle Olof Schreiber
Joel Petersson
Tomas Waldén
David Ahl
Stellan Sandler
Mia Phillipson
Lena Holm
iNOS-dependent increase in colonic mucus thickness in DSS-colitic rats.
PLoS ONE
author_facet Olof Schreiber
Joel Petersson
Tomas Waldén
David Ahl
Stellan Sandler
Mia Phillipson
Lena Holm
author_sort Olof Schreiber
title iNOS-dependent increase in colonic mucus thickness in DSS-colitic rats.
title_short iNOS-dependent increase in colonic mucus thickness in DSS-colitic rats.
title_full iNOS-dependent increase in colonic mucus thickness in DSS-colitic rats.
title_fullStr iNOS-dependent increase in colonic mucus thickness in DSS-colitic rats.
title_full_unstemmed iNOS-dependent increase in colonic mucus thickness in DSS-colitic rats.
title_sort inos-dependent increase in colonic mucus thickness in dss-colitic rats.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description AIM: To investigate colonic mucus thickness in vivo in health and during experimental inflammatory bowel disease. METHODS: Colitis was induced with 5% DSS in drinking water for 8 days prior to experiment, when the descending colonic mucosa of anesthetized rats was studied using intravital microscopy. Mucus thickness was measured with micropipettes attached to a micromanipulator. To assess the contributions of NOS and prostaglandins in the regulation of colonic mucus thickness, the non-selective NOS-inhibitor L-NNA (10 mg/kg bolus followed by 3 mg/kg/h), the selective iNOS-inhibitor L-NIL (10 mg/kg bolus followed by 3 mg/kg/h) and the non-selective COX-inhibitor diclofenac (5 mg/kg) were administered intravenously prior to experiment. To further investigate the role of iNOS in the regulation of colonic mucus thickness, iNOS -/- mice were used. RESULTS: Colitic rats had a thicker firmly adherent mucus layer following 8 days of DSS treatment than untreated rats (88±2 µm vs 76±1 µm). During induction of colitis, the thickness of the colonic mucus layer initially decreased but was from day 3 significantly thicker than in untreated rats. Diclofenac reduced the mucus thickness similarly in colitic and untreated rats (-16±5 µm vs -14±2 µm). While L-NNA had no effect on colonic mucus thickness in DSS or untreated controls (+3±2 µm vs +3±1 µm), L-NIL reduced the mucus thickness significantly more in colitic rats than in controls (-33±4 µm vs -10±3 µm). The importance of iNOS in regulating the colonic mucus thickness was confirmed in iNOS-/- mice, which had thinner colonic mucus than wild-type mice (35±3 µm vs 50±2 µm, respectively). Furthermore, immunohistochemistry revealed increased levels of iNOS in the colonic surface epithelium following DSS treatment. CONCLUSION: Both prostaglandins and nitric oxide regulate basal colonic mucus thickness. During onset of colitis, the thickness of the mucus layer is initially reduced followed by an iNOS mediated increase.
url http://europepmc.org/articles/PMC3747056?pdf=render
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