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Potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine

Alginate oligosaccharides (AOS) are natural bioactive compounds with anti-inflammatory properties. We performed a feeding trial employing a zebrafish (Danio rerio) model of soybean-induced intestinal inflammation. Five groups of fish were fed different diets: a control (CT) diet, a soybean meal (SBM...

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Autores principales: Rehman, Saima, Gora, Adnan H., Abdelhafiz, Yousri, Dias, Jorge, Pierre, Ronan, Meynen, Koen, Fernandes, Jorge M. O., Sørensen, Mette, Brugman, Sylvia, Kiron, Viswanath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235609/
https://www.ncbi.nlm.nih.gov/pubmed/37275890
http://dx.doi.org/10.3389/fimmu.2023.1183701
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author Rehman, Saima
Gora, Adnan H.
Abdelhafiz, Yousri
Dias, Jorge
Pierre, Ronan
Meynen, Koen
Fernandes, Jorge M. O.
Sørensen, Mette
Brugman, Sylvia
Kiron, Viswanath
author_facet Rehman, Saima
Gora, Adnan H.
Abdelhafiz, Yousri
Dias, Jorge
Pierre, Ronan
Meynen, Koen
Fernandes, Jorge M. O.
Sørensen, Mette
Brugman, Sylvia
Kiron, Viswanath
author_sort Rehman, Saima
collection PubMed
description Alginate oligosaccharides (AOS) are natural bioactive compounds with anti-inflammatory properties. We performed a feeding trial employing a zebrafish (Danio rerio) model of soybean-induced intestinal inflammation. Five groups of fish were fed different diets: a control (CT) diet, a soybean meal (SBM) diet, a soybean meal+β-glucan (BG) diet and 2 soybean meal+AOS diets (alginate products differing in the content of low molecular weight fractions - AL, with 31% < 3kDa and AH, with 3% < 3kDa). We analyzed the intestinal transcriptomic and plasma metabolomic profiles of the study groups. In addition, we assessed the expression of inflammatory marker genes and histological alterations in the intestine. Dietary algal β-(1, 3)-glucan and AOS were able to bring the expression of certain inflammatory genes altered by dietary SBM to a level similar to that in the control group. Intestinal transcriptomic analysis indicated that dietary SBM changed the expression of genes linked to inflammation, endoplasmic reticulum, reproduction and cell motility. The AL diet suppressed the expression of genes related to complement activation, inflammatory and humoral response, which can likely have an inflammation alleviation effect. On the other hand, the AH diet reduced the expression of genes, causing an enrichment of negative regulation of immune system process. The BG diet suppressed several immune genes linked to the endopeptidase activity and proteolysis. The plasma metabolomic profile further revealed that dietary SBM can alter inflammation-linked metabolites such as itaconic acid, taurochenodeoxycholic acid and enriched the arginine biosynthesis pathway. The diet AL helped in elevating one of the short chain fatty acids, namely 2-hydroxybutyric acid while the BG diet increased the abundance of a vitamin, pantothenic acid. Histological evaluation revealed the advantage of the AL diet: it increased the goblet cell number and length of villi of the intestinal mucosa. Overall, our results indicate that dietary AOS with an appropriate amount of < 3kDa can stall the inflammatory responses in zebrafish.
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spelling pubmed-102356092023-06-03 Potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine Rehman, Saima Gora, Adnan H. Abdelhafiz, Yousri Dias, Jorge Pierre, Ronan Meynen, Koen Fernandes, Jorge M. O. Sørensen, Mette Brugman, Sylvia Kiron, Viswanath Front Immunol Immunology Alginate oligosaccharides (AOS) are natural bioactive compounds with anti-inflammatory properties. We performed a feeding trial employing a zebrafish (Danio rerio) model of soybean-induced intestinal inflammation. Five groups of fish were fed different diets: a control (CT) diet, a soybean meal (SBM) diet, a soybean meal+β-glucan (BG) diet and 2 soybean meal+AOS diets (alginate products differing in the content of low molecular weight fractions - AL, with 31% < 3kDa and AH, with 3% < 3kDa). We analyzed the intestinal transcriptomic and plasma metabolomic profiles of the study groups. In addition, we assessed the expression of inflammatory marker genes and histological alterations in the intestine. Dietary algal β-(1, 3)-glucan and AOS were able to bring the expression of certain inflammatory genes altered by dietary SBM to a level similar to that in the control group. Intestinal transcriptomic analysis indicated that dietary SBM changed the expression of genes linked to inflammation, endoplasmic reticulum, reproduction and cell motility. The AL diet suppressed the expression of genes related to complement activation, inflammatory and humoral response, which can likely have an inflammation alleviation effect. On the other hand, the AH diet reduced the expression of genes, causing an enrichment of negative regulation of immune system process. The BG diet suppressed several immune genes linked to the endopeptidase activity and proteolysis. The plasma metabolomic profile further revealed that dietary SBM can alter inflammation-linked metabolites such as itaconic acid, taurochenodeoxycholic acid and enriched the arginine biosynthesis pathway. The diet AL helped in elevating one of the short chain fatty acids, namely 2-hydroxybutyric acid while the BG diet increased the abundance of a vitamin, pantothenic acid. Histological evaluation revealed the advantage of the AL diet: it increased the goblet cell number and length of villi of the intestinal mucosa. Overall, our results indicate that dietary AOS with an appropriate amount of < 3kDa can stall the inflammatory responses in zebrafish. Frontiers Media S.A. 2023-05-19 /pmc/articles/PMC10235609/ /pubmed/37275890 http://dx.doi.org/10.3389/fimmu.2023.1183701 Text en Copyright © 2023 Rehman, Gora, Abdelhafiz, Dias, Pierre, Meynen, Fernandes, Sørensen, Brugman and Kiron https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Rehman, Saima
Gora, Adnan H.
Abdelhafiz, Yousri
Dias, Jorge
Pierre, Ronan
Meynen, Koen
Fernandes, Jorge M. O.
Sørensen, Mette
Brugman, Sylvia
Kiron, Viswanath
Potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine
title Potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine
title_full Potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine
title_fullStr Potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine
title_full_unstemmed Potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine
title_short Potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine
title_sort potential of algae-derived alginate oligosaccharides and β-glucan to counter inflammation in adult zebrafish intestine
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235609/
https://www.ncbi.nlm.nih.gov/pubmed/37275890
http://dx.doi.org/10.3389/fimmu.2023.1183701
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