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Effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs
BACKGROUND: Sucralfate is a gastroprotectant with no known systemic effects. The efficacy of sucralfate for prevention and treatment of stress‐related mucosal diseases (SRMD) in dogs is unknown. HYPOTHESIS/OBJECTIVES: To develop a canine ex vivo model of SRMD and to determine the effect of sucralfat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866966/ https://www.ncbi.nlm.nih.gov/pubmed/29460464 http://dx.doi.org/10.1111/jvim.15076 |
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author | Hill, Tracy L. Lascelles, B. Duncan X. Blikslager, Anthony T. |
author_facet | Hill, Tracy L. Lascelles, B. Duncan X. Blikslager, Anthony T. |
author_sort | Hill, Tracy L. |
collection | PubMed |
description | BACKGROUND: Sucralfate is a gastroprotectant with no known systemic effects. The efficacy of sucralfate for prevention and treatment of stress‐related mucosal diseases (SRMD) in dogs is unknown. HYPOTHESIS/OBJECTIVES: To develop a canine ex vivo model of SRMD and to determine the effect of sucralfate on mucosal barrier function in this model. ANIMALS: Gastric antral mucosa was collected immediately postmortem from 29 random‐source apparently healthy dogs euthanized at a local animal control facility. METHODS: Randomized experimental trial. Sucralfate (100 mg/mL) was applied to ex vivo canine gastric mucosa concurrent with and after acid injury. Barrier function was assessed by measurement of transepithelial electrical resistance (TER) and radiolabeled mannitol flux. RESULTS: Application of acidified Ringers solution to the mucosal side of gastric antrum caused a reduction in gastric barrier function, and washout of acidified Ringers solution allowed recovery of barrier function (TER: 34.0 ± 2.8% of control at maximum injury, 71.3 ± 5.5% at recovery, P < .001). Sucralfate application at the time of injury or after injury significantly hastened recovery of barrier function (TER: 118.0 ± 15.2% of control at maximum injury, P < .001 and 111.0 ± 15.5% at recovery, P = .35). CONCLUSIONS AND CLINICAL IMPORTANCE: Sucralfate appeared effective at restoring defects in gastric barrier function induced by acid and accelerating repair of tissues subjected to acid in this model, suggesting that sucralfate could have utility for the treatment and prevention of SRMD in dogs. |
format | Online Article Text |
id | pubmed-5866966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58669662018-03-28 Effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs Hill, Tracy L. Lascelles, B. Duncan X. Blikslager, Anthony T. J Vet Intern Med SMALL ANIMAL BACKGROUND: Sucralfate is a gastroprotectant with no known systemic effects. The efficacy of sucralfate for prevention and treatment of stress‐related mucosal diseases (SRMD) in dogs is unknown. HYPOTHESIS/OBJECTIVES: To develop a canine ex vivo model of SRMD and to determine the effect of sucralfate on mucosal barrier function in this model. ANIMALS: Gastric antral mucosa was collected immediately postmortem from 29 random‐source apparently healthy dogs euthanized at a local animal control facility. METHODS: Randomized experimental trial. Sucralfate (100 mg/mL) was applied to ex vivo canine gastric mucosa concurrent with and after acid injury. Barrier function was assessed by measurement of transepithelial electrical resistance (TER) and radiolabeled mannitol flux. RESULTS: Application of acidified Ringers solution to the mucosal side of gastric antrum caused a reduction in gastric barrier function, and washout of acidified Ringers solution allowed recovery of barrier function (TER: 34.0 ± 2.8% of control at maximum injury, 71.3 ± 5.5% at recovery, P < .001). Sucralfate application at the time of injury or after injury significantly hastened recovery of barrier function (TER: 118.0 ± 15.2% of control at maximum injury, P < .001 and 111.0 ± 15.5% at recovery, P = .35). CONCLUSIONS AND CLINICAL IMPORTANCE: Sucralfate appeared effective at restoring defects in gastric barrier function induced by acid and accelerating repair of tissues subjected to acid in this model, suggesting that sucralfate could have utility for the treatment and prevention of SRMD in dogs. John Wiley and Sons Inc. 2018-02-20 2018 /pmc/articles/PMC5866966/ /pubmed/29460464 http://dx.doi.org/10.1111/jvim.15076 Text en Copyright © 2018 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | SMALL ANIMAL Hill, Tracy L. Lascelles, B. Duncan X. Blikslager, Anthony T. Effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs |
title | Effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs |
title_full | Effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs |
title_fullStr | Effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs |
title_full_unstemmed | Effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs |
title_short | Effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs |
title_sort | effect of sucralfate on gastric permeability in an ex vivo model of stress‐related mucosal disease in dogs |
topic | SMALL ANIMAL |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866966/ https://www.ncbi.nlm.nih.gov/pubmed/29460464 http://dx.doi.org/10.1111/jvim.15076 |
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