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Dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats

Evidence suggests that gut microbiota dysbiosis plays a critical role in the initiation and promotion of inflammatory bowel disease (IBD). Kefir is a fermented dairy product including yeast and bacterial species. We aimed to investigate the effect of kefir on trinitrobenzene sulfonic acid (TNBS)‐ind...

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Autores principales: Sevencan, Nurhayat Ozkan, Isler, Mehmet, Kapucuoglu, Fatma Nilgun, Senol, Altug, Kayhan, Burcak, Kiztanir, Sefa, Kockar, Muhammed Cem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766543/
https://www.ncbi.nlm.nih.gov/pubmed/31572604
http://dx.doi.org/10.1002/fsn3.1174
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author Sevencan, Nurhayat Ozkan
Isler, Mehmet
Kapucuoglu, Fatma Nilgun
Senol, Altug
Kayhan, Burcak
Kiztanir, Sefa
Kockar, Muhammed Cem
author_facet Sevencan, Nurhayat Ozkan
Isler, Mehmet
Kapucuoglu, Fatma Nilgun
Senol, Altug
Kayhan, Burcak
Kiztanir, Sefa
Kockar, Muhammed Cem
author_sort Sevencan, Nurhayat Ozkan
collection PubMed
description Evidence suggests that gut microbiota dysbiosis plays a critical role in the initiation and promotion of inflammatory bowel disease (IBD). Kefir is a fermented dairy product including yeast and bacterial species. We aimed to investigate the effect of kefir on trinitrobenzene sulfonic acid (TNBS)‐induced colitis in rats using two different doses. Fifty‐four Wistar rats were divided into six groups. For 14 days, the normal control and colitis control groups were given tap water, kefir10 control, kefir10 colitis, and kefir30 control, and the kefir30 colitis groups were given phosphate‐buffered saline containing 10% or 30% kefir, respectively, instead of tap water. Colitis was induced by intracolonically administrating TNBS in the colitis control, kefir10 colitis, and kefir30 colitis groups. On the 14th day, the rats were sacrificed. The weights and lengths of the colons were measured and macroscopically evaluated, and the distal 10 cm segments were subjected to a histopathological examination. The incidence of bloody stool and diarrhea in the kefir10 colitis group was found to be less than the colitis control and kefir30 colitis groups. The colonic weight/length ratio in the kefir10 colitis group was lower than that in the colitis control and kefir30 colitis groups. We detected that the 10% kefir treatment reduced TNBS‐induced macroscopic colonic damage, while it was exacerbated by the 30% kefir treatment. No significant difference was observed between the colitis groups in terms of microscopic colonic damage scoring. These results indicate that kefir, with a careful dose selection, may be a useful agent in the treatment of IBD.
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spelling pubmed-67665432019-09-30 Dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats Sevencan, Nurhayat Ozkan Isler, Mehmet Kapucuoglu, Fatma Nilgun Senol, Altug Kayhan, Burcak Kiztanir, Sefa Kockar, Muhammed Cem Food Sci Nutr Original Research Evidence suggests that gut microbiota dysbiosis plays a critical role in the initiation and promotion of inflammatory bowel disease (IBD). Kefir is a fermented dairy product including yeast and bacterial species. We aimed to investigate the effect of kefir on trinitrobenzene sulfonic acid (TNBS)‐induced colitis in rats using two different doses. Fifty‐four Wistar rats were divided into six groups. For 14 days, the normal control and colitis control groups were given tap water, kefir10 control, kefir10 colitis, and kefir30 control, and the kefir30 colitis groups were given phosphate‐buffered saline containing 10% or 30% kefir, respectively, instead of tap water. Colitis was induced by intracolonically administrating TNBS in the colitis control, kefir10 colitis, and kefir30 colitis groups. On the 14th day, the rats were sacrificed. The weights and lengths of the colons were measured and macroscopically evaluated, and the distal 10 cm segments were subjected to a histopathological examination. The incidence of bloody stool and diarrhea in the kefir10 colitis group was found to be less than the colitis control and kefir30 colitis groups. The colonic weight/length ratio in the kefir10 colitis group was lower than that in the colitis control and kefir30 colitis groups. We detected that the 10% kefir treatment reduced TNBS‐induced macroscopic colonic damage, while it was exacerbated by the 30% kefir treatment. No significant difference was observed between the colitis groups in terms of microscopic colonic damage scoring. These results indicate that kefir, with a careful dose selection, may be a useful agent in the treatment of IBD. John Wiley and Sons Inc. 2019-08-22 /pmc/articles/PMC6766543/ /pubmed/31572604 http://dx.doi.org/10.1002/fsn3.1174 Text en © 2019 The Authors. Food Science & Nutrition published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Sevencan, Nurhayat Ozkan
Isler, Mehmet
Kapucuoglu, Fatma Nilgun
Senol, Altug
Kayhan, Burcak
Kiztanir, Sefa
Kockar, Muhammed Cem
Dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats
title Dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats
title_full Dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats
title_fullStr Dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats
title_full_unstemmed Dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats
title_short Dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats
title_sort dose‐dependent effects of kefir on colitis induced by trinitrobenzene sulfonic acid in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766543/
https://www.ncbi.nlm.nih.gov/pubmed/31572604
http://dx.doi.org/10.1002/fsn3.1174
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