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Effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis
BACKGROUND: Inflammatory bowel diseases (IBD) are chronic intestinal inflammatory diseases affecting about 1% of western populations. New eating behaviors might contribute to the global emergence of IBD. Although the immunoregulatory effects of omega-3 fatty acids have been well characterized in vit...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691874/ https://www.ncbi.nlm.nih.gov/pubmed/23725086 http://dx.doi.org/10.1186/1476-511X-12-81 |
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author | Bosco, Nabil Brahmbhatt, Viral Oliveira, Manuel Martin, Francois-Pierre Lichti, Pia Raymond, Frederic Mansourian, Robert Metairon, Sylviane Pace-Asciak, Cecil Bastic Schmid, Viktoria Rezzi, Serge Haller, Dirk Benyacoub, Jalil |
author_facet | Bosco, Nabil Brahmbhatt, Viral Oliveira, Manuel Martin, Francois-Pierre Lichti, Pia Raymond, Frederic Mansourian, Robert Metairon, Sylviane Pace-Asciak, Cecil Bastic Schmid, Viktoria Rezzi, Serge Haller, Dirk Benyacoub, Jalil |
author_sort | Bosco, Nabil |
collection | PubMed |
description | BACKGROUND: Inflammatory bowel diseases (IBD) are chronic intestinal inflammatory diseases affecting about 1% of western populations. New eating behaviors might contribute to the global emergence of IBD. Although the immunoregulatory effects of omega-3 fatty acids have been well characterized in vitro, their role in IBD is controversial. METHODS: The aim of this study was to assess the impact of increased fish oil intake on colonic gene expression, eicosanoid metabolism and development of colitis in a mouse model of IBD. Rag-2 deficient mice were fed fish oil (FO) enriched in omega-3 fatty acids i.e. EPA and DHA or control diet for 4 weeks before colitis induction by adoptive transfer of naïve T cells and maintained in the same diet for 4 additional weeks. Onset of colitis was monitored by colonoscopy and further confirmed by immunological examinations. Whole genome expression profiling was made and eicosanoids were measured by HPLC-MS/MS in colonic samples. RESULTS: A significant reduction of colonic proinflammatory eicosanoids in FO fed mice compared to control was observed. However, neither alteration of colonic gene expression signature nor reduction in IBD scores was observed under FO diet. CONCLUSION: Thus, increased intake of dietary FO did not prevent experimental colitis. |
format | Online Article Text |
id | pubmed-3691874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36918742013-06-26 Effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis Bosco, Nabil Brahmbhatt, Viral Oliveira, Manuel Martin, Francois-Pierre Lichti, Pia Raymond, Frederic Mansourian, Robert Metairon, Sylviane Pace-Asciak, Cecil Bastic Schmid, Viktoria Rezzi, Serge Haller, Dirk Benyacoub, Jalil Lipids Health Dis Research BACKGROUND: Inflammatory bowel diseases (IBD) are chronic intestinal inflammatory diseases affecting about 1% of western populations. New eating behaviors might contribute to the global emergence of IBD. Although the immunoregulatory effects of omega-3 fatty acids have been well characterized in vitro, their role in IBD is controversial. METHODS: The aim of this study was to assess the impact of increased fish oil intake on colonic gene expression, eicosanoid metabolism and development of colitis in a mouse model of IBD. Rag-2 deficient mice were fed fish oil (FO) enriched in omega-3 fatty acids i.e. EPA and DHA or control diet for 4 weeks before colitis induction by adoptive transfer of naïve T cells and maintained in the same diet for 4 additional weeks. Onset of colitis was monitored by colonoscopy and further confirmed by immunological examinations. Whole genome expression profiling was made and eicosanoids were measured by HPLC-MS/MS in colonic samples. RESULTS: A significant reduction of colonic proinflammatory eicosanoids in FO fed mice compared to control was observed. However, neither alteration of colonic gene expression signature nor reduction in IBD scores was observed under FO diet. CONCLUSION: Thus, increased intake of dietary FO did not prevent experimental colitis. BioMed Central 2013-05-31 /pmc/articles/PMC3691874/ /pubmed/23725086 http://dx.doi.org/10.1186/1476-511X-12-81 Text en Copyright © 2013 Bosco 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 cited. |
spellingShingle | Research Bosco, Nabil Brahmbhatt, Viral Oliveira, Manuel Martin, Francois-Pierre Lichti, Pia Raymond, Frederic Mansourian, Robert Metairon, Sylviane Pace-Asciak, Cecil Bastic Schmid, Viktoria Rezzi, Serge Haller, Dirk Benyacoub, Jalil Effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis |
title | Effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis |
title_full | Effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis |
title_fullStr | Effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis |
title_full_unstemmed | Effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis |
title_short | Effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis |
title_sort | effects of increase in fish oil intake on intestinal eicosanoids and inflammation in a mouse model of colitis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691874/ https://www.ncbi.nlm.nih.gov/pubmed/23725086 http://dx.doi.org/10.1186/1476-511X-12-81 |
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