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Indomethacin-induced gastric damage in rats and the protective effect of donkey milk

INTRODUCTION: Indomethacin is an anti-inflammatory drug with clearly known side effects on gastric mucosa. New treatment and side effect prevention methods are being studied. Donkey milk, as a nutritional support, has recently come into the spotlight with its anti-oxidant features, high antibody con...

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Autores principales: Tastekin, Ebru, Ayvaz, Suleyman, Usta, Ufuk, Aydogdu, Nurettin, Cancilar, Ekrem, Puyan, Fulya Oz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949905/
https://www.ncbi.nlm.nih.gov/pubmed/29765456
http://dx.doi.org/10.5114/aoms.2016.59645
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author Tastekin, Ebru
Ayvaz, Suleyman
Usta, Ufuk
Aydogdu, Nurettin
Cancilar, Ekrem
Puyan, Fulya Oz
author_facet Tastekin, Ebru
Ayvaz, Suleyman
Usta, Ufuk
Aydogdu, Nurettin
Cancilar, Ekrem
Puyan, Fulya Oz
author_sort Tastekin, Ebru
collection PubMed
description INTRODUCTION: Indomethacin is an anti-inflammatory drug with clearly known side effects on gastric mucosa. New treatment and side effect prevention methods are being studied. Donkey milk, as a nutritional support, has recently come into the spotlight with its anti-oxidant features, high antibody content and low allergenic properties. In this study, we investigated donkey milk’s possible protective effect against acute gastric mucosal damage by indomethacin. MATERIAL AND METHODS: Four groups, each composed of 8 rats, were created. Rats in the first and third groups were fed with standard rat chow, while those in the second and fourth groups were additionally fed with 25 mg/kg of donkey milk per day via nasogastric gavage. On the 11(th) day gastric mucosal damage was induced by oral administration of 30 mg/kg of indomethacin to the rats in groups 3 and 4. Six h later all rats were sacrificed and their stomachs were removed for macroscopic and microscopic evaluation as well as biochemical examination of glutathione (GSH) and malondialdehyde (MDA) levels. Tumor necrosis factor-α (TNF-α) expression in the gastric mucosa was evaluated immunohistochemically. RESULTS: In the donkey milk-indomethacin group, total area of erosion and degree of linear ulceration were significantly lower than in the standard food-indomethacin group (p < 0.05). Also, GSH levels were increased and MDA levels were decreased significantly in this group. Tumor necrosis factor-α expression was more prevalent and stronger in the gastritis group, while lower expression was observed in the donkey milk group. CONCLUSIONS: Donkey milk was observed to have significant protective effects against gastric damage induced by indomethacin.
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spelling pubmed-59499052018-05-14 Indomethacin-induced gastric damage in rats and the protective effect of donkey milk Tastekin, Ebru Ayvaz, Suleyman Usta, Ufuk Aydogdu, Nurettin Cancilar, Ekrem Puyan, Fulya Oz Arch Med Sci Experimental Research INTRODUCTION: Indomethacin is an anti-inflammatory drug with clearly known side effects on gastric mucosa. New treatment and side effect prevention methods are being studied. Donkey milk, as a nutritional support, has recently come into the spotlight with its anti-oxidant features, high antibody content and low allergenic properties. In this study, we investigated donkey milk’s possible protective effect against acute gastric mucosal damage by indomethacin. MATERIAL AND METHODS: Four groups, each composed of 8 rats, were created. Rats in the first and third groups were fed with standard rat chow, while those in the second and fourth groups were additionally fed with 25 mg/kg of donkey milk per day via nasogastric gavage. On the 11(th) day gastric mucosal damage was induced by oral administration of 30 mg/kg of indomethacin to the rats in groups 3 and 4. Six h later all rats were sacrificed and their stomachs were removed for macroscopic and microscopic evaluation as well as biochemical examination of glutathione (GSH) and malondialdehyde (MDA) levels. Tumor necrosis factor-α (TNF-α) expression in the gastric mucosa was evaluated immunohistochemically. RESULTS: In the donkey milk-indomethacin group, total area of erosion and degree of linear ulceration were significantly lower than in the standard food-indomethacin group (p < 0.05). Also, GSH levels were increased and MDA levels were decreased significantly in this group. Tumor necrosis factor-α expression was more prevalent and stronger in the gastritis group, while lower expression was observed in the donkey milk group. CONCLUSIONS: Donkey milk was observed to have significant protective effects against gastric damage induced by indomethacin. Termedia Publishing House 2016-05-20 2018-04 /pmc/articles/PMC5949905/ /pubmed/29765456 http://dx.doi.org/10.5114/aoms.2016.59645 Text en Copyright: © 2016 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Experimental Research
Tastekin, Ebru
Ayvaz, Suleyman
Usta, Ufuk
Aydogdu, Nurettin
Cancilar, Ekrem
Puyan, Fulya Oz
Indomethacin-induced gastric damage in rats and the protective effect of donkey milk
title Indomethacin-induced gastric damage in rats and the protective effect of donkey milk
title_full Indomethacin-induced gastric damage in rats and the protective effect of donkey milk
title_fullStr Indomethacin-induced gastric damage in rats and the protective effect of donkey milk
title_full_unstemmed Indomethacin-induced gastric damage in rats and the protective effect of donkey milk
title_short Indomethacin-induced gastric damage in rats and the protective effect of donkey milk
title_sort indomethacin-induced gastric damage in rats and the protective effect of donkey milk
topic Experimental Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949905/
https://www.ncbi.nlm.nih.gov/pubmed/29765456
http://dx.doi.org/10.5114/aoms.2016.59645
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