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Effects of a soluble dietary fibre NUTRIOSE® on colonic fermentation and excretion rates in rats

The resistant dextrin NUTRIOSE®, developed from starch, is expected to act as a prebiotic. The aim of this study was to determine the effects of NUTRIOSE® on cecal parameters, short-chain fatty acid (SCFA) concentrations, and fecal excretion in rats. In an initial experiment, twenty-four male Fische...

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Autores principales: Guerin-Deremaux, Laetitia, Ringard, Florence, Desailly, Fabrice, Wils, Daniel
Formato: Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3029787/
https://www.ncbi.nlm.nih.gov/pubmed/21286404
http://dx.doi.org/10.4162/nrp.2010.4.6.470
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author Guerin-Deremaux, Laetitia
Ringard, Florence
Desailly, Fabrice
Wils, Daniel
author_facet Guerin-Deremaux, Laetitia
Ringard, Florence
Desailly, Fabrice
Wils, Daniel
author_sort Guerin-Deremaux, Laetitia
collection PubMed
description The resistant dextrin NUTRIOSE®, developed from starch, is expected to act as a prebiotic. The aim of this study was to determine the effects of NUTRIOSE® on cecal parameters, short-chain fatty acid (SCFA) concentrations, and fecal excretion in rats. In an initial experiment, twenty-four male Fischer F344 rats were randomly assigned to one of the following four treatments for 14 days: G0 (control diet), G2.5 (control diet + 2.5% of dextrin), G5 (control diet + 5% of dextrin), and G10 (control diet + 10% of dextrin). After 14 days, total cecal weight, cecal content, and cecal wall weight were significantly increased in G5 and G10 compared to G0. At the same time, cecal pH was significantly lower in G10 compared to G0. Total SCFA concentration was significantly higher in G10 than in G5, G2.5, and G0, and significantly higher in G5 than in G0. Acetate, butyrate, and propionate concentrations were significantly increased in G5 and G10 compared to the controls. In a second trial based on a similar design, eighteen male Fischer F344 rats were treated with a control diet supplemented with 5% of dextrin or 5% of fructo-oligosaccharide. The results obtained with NUTRIOSE® were similar to those obtained with the fructo-oligosaccharide. In a third experiment, two groups of 5 Fischer F344 rats were orally treated with 100 and 1,000 mg/kg NUTRIOSE®, respectively, and from 18% to 25% of the dextrin was excreted in the feces. The results of these three studies show that the consumption of NUTRIOSE®, by its effects on total cecal weight, cecal content, cecal wall weight, pH, and SCFA production, could induce healthy benefits since these effects are reported to be prebiotic effects.
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spelling pubmed-30297872011-01-31 Effects of a soluble dietary fibre NUTRIOSE® on colonic fermentation and excretion rates in rats Guerin-Deremaux, Laetitia Ringard, Florence Desailly, Fabrice Wils, Daniel Nutr Res Pract Original Research The resistant dextrin NUTRIOSE®, developed from starch, is expected to act as a prebiotic. The aim of this study was to determine the effects of NUTRIOSE® on cecal parameters, short-chain fatty acid (SCFA) concentrations, and fecal excretion in rats. In an initial experiment, twenty-four male Fischer F344 rats were randomly assigned to one of the following four treatments for 14 days: G0 (control diet), G2.5 (control diet + 2.5% of dextrin), G5 (control diet + 5% of dextrin), and G10 (control diet + 10% of dextrin). After 14 days, total cecal weight, cecal content, and cecal wall weight were significantly increased in G5 and G10 compared to G0. At the same time, cecal pH was significantly lower in G10 compared to G0. Total SCFA concentration was significantly higher in G10 than in G5, G2.5, and G0, and significantly higher in G5 than in G0. Acetate, butyrate, and propionate concentrations were significantly increased in G5 and G10 compared to the controls. In a second trial based on a similar design, eighteen male Fischer F344 rats were treated with a control diet supplemented with 5% of dextrin or 5% of fructo-oligosaccharide. The results obtained with NUTRIOSE® were similar to those obtained with the fructo-oligosaccharide. In a third experiment, two groups of 5 Fischer F344 rats were orally treated with 100 and 1,000 mg/kg NUTRIOSE®, respectively, and from 18% to 25% of the dextrin was excreted in the feces. The results of these three studies show that the consumption of NUTRIOSE®, by its effects on total cecal weight, cecal content, cecal wall weight, pH, and SCFA production, could induce healthy benefits since these effects are reported to be prebiotic effects. The Korean Nutrition Society and the Korean Society of Community Nutrition 2010-12 2010-12-28 /pmc/articles/PMC3029787/ /pubmed/21286404 http://dx.doi.org/10.4162/nrp.2010.4.6.470 Text en ©2010 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Guerin-Deremaux, Laetitia
Ringard, Florence
Desailly, Fabrice
Wils, Daniel
Effects of a soluble dietary fibre NUTRIOSE® on colonic fermentation and excretion rates in rats
title Effects of a soluble dietary fibre NUTRIOSE® on colonic fermentation and excretion rates in rats
title_full Effects of a soluble dietary fibre NUTRIOSE® on colonic fermentation and excretion rates in rats
title_fullStr Effects of a soluble dietary fibre NUTRIOSE® on colonic fermentation and excretion rates in rats
title_full_unstemmed Effects of a soluble dietary fibre NUTRIOSE® on colonic fermentation and excretion rates in rats
title_short Effects of a soluble dietary fibre NUTRIOSE® on colonic fermentation and excretion rates in rats
title_sort effects of a soluble dietary fibre nutriose® on colonic fermentation and excretion rates in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3029787/
https://www.ncbi.nlm.nih.gov/pubmed/21286404
http://dx.doi.org/10.4162/nrp.2010.4.6.470
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