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Novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice
Studies have documented the benefits of fish oil in different diseases because of its high n‐3 polyunsaturated fatty acid content. However, these studies mostly used commercially available fish oil supplements with a ratio of 18/12 for eicosapentaenoic acid and docosahexaenoic acid (DHA). However, i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723182/ https://www.ncbi.nlm.nih.gov/pubmed/33312536 http://dx.doi.org/10.1002/fsn3.1941 |
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author | Zhang, Jing Yi, Congmin Han, Jiaojiao Ming, Tinghong Zhou, Jun Lu, Chenyang Li, Ye Su, Xiurong |
author_facet | Zhang, Jing Yi, Congmin Han, Jiaojiao Ming, Tinghong Zhou, Jun Lu, Chenyang Li, Ye Su, Xiurong |
author_sort | Zhang, Jing |
collection | PubMed |
description | Studies have documented the benefits of fish oil in different diseases because of its high n‐3 polyunsaturated fatty acid content. However, these studies mostly used commercially available fish oil supplements with a ratio of 18/12 for eicosapentaenoic acid and docosahexaenoic acid (DHA). However, increasing DHA content for this commonly used ratio might bring out a varied metabolic effect, which have remained unclear. Thus, in this study, a novel tuna oil (TO) was applied to investigate the effect of high‐DHA content on the alteration of the gut microbiota and obesity in high‐fat diet mice. The results suggest that high‐DHA TO (HDTO) supplementation notably ameliorates obesity and related lipid parameters and restores the expression of lipid metabolism‐related genes. The benefits of TOs were derived from their modification of the gut microbiota composition and structure in mice. A high‐fat diet triggered an increased Firmicutes/Bacteroidetes ratio that was remarkably restored by TOs. The number of obesity‐promoting bacteria—Desulfovibrio, Paraeggerthella, Terrisporobacter, Millionella, Lachnoclostridium, Anaerobacterium, and Ruminiclostridium—was dramatically reduced. Desulfovibrio desulfuricans, Alistipes putredinis, and Millionella massiliensis, three dysbiosis‐related species, were especially regulated by HDTO. Regarding the prevention of obesity, HDTO outperforms the normal TO. Intriguingly, HDTO feeding to HFD‐fed mice might alter the arginine and proline metabolism of intestinal microbiota. |
format | Online Article Text |
id | pubmed-7723182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77231822020-12-11 Novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice Zhang, Jing Yi, Congmin Han, Jiaojiao Ming, Tinghong Zhou, Jun Lu, Chenyang Li, Ye Su, Xiurong Food Sci Nutr Original Research Studies have documented the benefits of fish oil in different diseases because of its high n‐3 polyunsaturated fatty acid content. However, these studies mostly used commercially available fish oil supplements with a ratio of 18/12 for eicosapentaenoic acid and docosahexaenoic acid (DHA). However, increasing DHA content for this commonly used ratio might bring out a varied metabolic effect, which have remained unclear. Thus, in this study, a novel tuna oil (TO) was applied to investigate the effect of high‐DHA content on the alteration of the gut microbiota and obesity in high‐fat diet mice. The results suggest that high‐DHA TO (HDTO) supplementation notably ameliorates obesity and related lipid parameters and restores the expression of lipid metabolism‐related genes. The benefits of TOs were derived from their modification of the gut microbiota composition and structure in mice. A high‐fat diet triggered an increased Firmicutes/Bacteroidetes ratio that was remarkably restored by TOs. The number of obesity‐promoting bacteria—Desulfovibrio, Paraeggerthella, Terrisporobacter, Millionella, Lachnoclostridium, Anaerobacterium, and Ruminiclostridium—was dramatically reduced. Desulfovibrio desulfuricans, Alistipes putredinis, and Millionella massiliensis, three dysbiosis‐related species, were especially regulated by HDTO. Regarding the prevention of obesity, HDTO outperforms the normal TO. Intriguingly, HDTO feeding to HFD‐fed mice might alter the arginine and proline metabolism of intestinal microbiota. John Wiley and Sons Inc. 2020-11-07 /pmc/articles/PMC7723182/ /pubmed/33312536 http://dx.doi.org/10.1002/fsn3.1941 Text en © 2020 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC 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 Zhang, Jing Yi, Congmin Han, Jiaojiao Ming, Tinghong Zhou, Jun Lu, Chenyang Li, Ye Su, Xiurong Novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice |
title | Novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice |
title_full | Novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice |
title_fullStr | Novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice |
title_full_unstemmed | Novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice |
title_short | Novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice |
title_sort | novel high‐docosahexaenoic‐acid tuna oil supplementation modulates gut microbiota and alleviates obesity in high‐fat diet mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723182/ https://www.ncbi.nlm.nih.gov/pubmed/33312536 http://dx.doi.org/10.1002/fsn3.1941 |
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