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Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice
BACKGROUND: The antimetabolite chemotherapy 5-Fluorouracil is one of the most commonly prescribed drugs in clinical cancer treatment. Although this drug is not specific for cancer cells and also acts on healthy cells, it can cause mucositis, a common collateral effect. Dysbiosis has also been descri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004512/ https://www.ncbi.nlm.nih.gov/pubmed/24721659 http://dx.doi.org/10.1186/1477-5751-13-6 |
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author | Maioli, Tatiani Uceli de Melo Silva, Brenda Dias, Michelle Nobre Paiva, Nivea Carolina Cardoso, Valbert Nascimento Fernandes, Simone Odilia Carneiro, Cláudia Martins dos Santos Martins, Flaviano de Vasconcelos Generoso, Simone |
author_facet | Maioli, Tatiani Uceli de Melo Silva, Brenda Dias, Michelle Nobre Paiva, Nivea Carolina Cardoso, Valbert Nascimento Fernandes, Simone Odilia Carneiro, Cláudia Martins dos Santos Martins, Flaviano de Vasconcelos Generoso, Simone |
author_sort | Maioli, Tatiani Uceli |
collection | PubMed |
description | BACKGROUND: The antimetabolite chemotherapy 5-Fluorouracil is one of the most commonly prescribed drugs in clinical cancer treatment. Although this drug is not specific for cancer cells and also acts on healthy cells, it can cause mucositis, a common collateral effect. Dysbiosis has also been described in 5-fluorouracil-induced mucositis and is likely to contribute to the overall development of mucositis. In light of this theory, the use of probiotics could be a helpful strategy to alleviate mucositis. So the aim of this study was evaluate the impact of the probiotic Saccharomyces boulardii in a model of mucositis. RESULTS: After induced of mucositis, mice from the Mucositis groups showed a decrease in food consumption (p < 0.05) and therefore had a greater weight loss (p < 0.05). The treatment with Saccharomyces boulardii did not reverse this effect (p > 0.05). Mucositis induced an increase in intestinal permeability and intestinal inflammation (p < 0.05). There were no differences in mucosal lesions, intestinal permeability and sIgA secretion (p > 0.05) in mice pretreated with S. boulardii. CONCLUSIONS: S. boulardii was not able to prevent the effects of experimental mucositis induced by 5- Fluorouracil. |
format | Online Article Text |
id | pubmed-4004512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40045122014-04-30 Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice Maioli, Tatiani Uceli de Melo Silva, Brenda Dias, Michelle Nobre Paiva, Nivea Carolina Cardoso, Valbert Nascimento Fernandes, Simone Odilia Carneiro, Cláudia Martins dos Santos Martins, Flaviano de Vasconcelos Generoso, Simone J Negat Results Biomed Research BACKGROUND: The antimetabolite chemotherapy 5-Fluorouracil is one of the most commonly prescribed drugs in clinical cancer treatment. Although this drug is not specific for cancer cells and also acts on healthy cells, it can cause mucositis, a common collateral effect. Dysbiosis has also been described in 5-fluorouracil-induced mucositis and is likely to contribute to the overall development of mucositis. In light of this theory, the use of probiotics could be a helpful strategy to alleviate mucositis. So the aim of this study was evaluate the impact of the probiotic Saccharomyces boulardii in a model of mucositis. RESULTS: After induced of mucositis, mice from the Mucositis groups showed a decrease in food consumption (p < 0.05) and therefore had a greater weight loss (p < 0.05). The treatment with Saccharomyces boulardii did not reverse this effect (p > 0.05). Mucositis induced an increase in intestinal permeability and intestinal inflammation (p < 0.05). There were no differences in mucosal lesions, intestinal permeability and sIgA secretion (p > 0.05) in mice pretreated with S. boulardii. CONCLUSIONS: S. boulardii was not able to prevent the effects of experimental mucositis induced by 5- Fluorouracil. BioMed Central 2014-04-11 /pmc/articles/PMC4004512/ /pubmed/24721659 http://dx.doi.org/10.1186/1477-5751-13-6 Text en Copyright © 2014 Maioli et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Maioli, Tatiani Uceli de Melo Silva, Brenda Dias, Michelle Nobre Paiva, Nivea Carolina Cardoso, Valbert Nascimento Fernandes, Simone Odilia Carneiro, Cláudia Martins dos Santos Martins, Flaviano de Vasconcelos Generoso, Simone Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice |
title | Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice |
title_full | Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice |
title_fullStr | Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice |
title_full_unstemmed | Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice |
title_short | Pretreatment with Saccharomyces boulardii does not prevent the experimental mucositis in Swiss mice |
title_sort | pretreatment with saccharomyces boulardii does not prevent the experimental mucositis in swiss mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004512/ https://www.ncbi.nlm.nih.gov/pubmed/24721659 http://dx.doi.org/10.1186/1477-5751-13-6 |
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