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Effect of the Novel Polysaccharide PolyGlycopleX(®) on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large Intestine

Many of the health benefits associated with dietary fiber are attributed to their fermentation by microbiota and production of short chain fatty acids (SCFA). The aim of this study was to investigate the fermentability of the functional fiber PolyGlyopleX(®) (PGX(®)) in vitro. A validated dynamic, c...

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Autores principales: Reimer, Raylene A., Maathuis, Annet J. H., Venema, Koen, Lyon, Michael R., Gahler, Roland J., Wood, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967181/
https://www.ncbi.nlm.nih.gov/pubmed/24638070
http://dx.doi.org/10.3390/nu6031115
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author Reimer, Raylene A.
Maathuis, Annet J. H.
Venema, Koen
Lyon, Michael R.
Gahler, Roland J.
Wood, Simon
author_facet Reimer, Raylene A.
Maathuis, Annet J. H.
Venema, Koen
Lyon, Michael R.
Gahler, Roland J.
Wood, Simon
author_sort Reimer, Raylene A.
collection PubMed
description Many of the health benefits associated with dietary fiber are attributed to their fermentation by microbiota and production of short chain fatty acids (SCFA). The aim of this study was to investigate the fermentability of the functional fiber PolyGlyopleX(®) (PGX(®)) in vitro. A validated dynamic, computer-controlled in vitro system simulating the conditions in the proximal large intestine (TIM-2) was used. Sodium hydroxide (NaOH) consumption in the system was used as an indicator of fermentability and SCFA and branched chain fatty acids (BCFA) production was determined. NaOH consumption was significantly higher for Fructooligosaccharide (FOS) than PGX, which was higher than cellulose (p = 0.002). At 32, 48 and 72 h, acetate and butyrate production were higher for FOS and PGX versus cellulose. Propionate production was higher for PGX than cellulose at 32, 48, 56 and 72 h and higher than FOS at 72 h (p = 0.014). Total BCFA production was lower for FOS compared to cellulose, whereas production with PGX was lower than for cellulose at 72 h. In conclusion, PGX is fermented by the colonic microbiota which appeared to adapt to the substrate over time. The greater propionate production for PGX may explain part of the cholesterol-lowering properties of PGX seen in rodents and humans.
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spelling pubmed-39671812014-03-27 Effect of the Novel Polysaccharide PolyGlycopleX(®) on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large Intestine Reimer, Raylene A. Maathuis, Annet J. H. Venema, Koen Lyon, Michael R. Gahler, Roland J. Wood, Simon Nutrients Article Many of the health benefits associated with dietary fiber are attributed to their fermentation by microbiota and production of short chain fatty acids (SCFA). The aim of this study was to investigate the fermentability of the functional fiber PolyGlyopleX(®) (PGX(®)) in vitro. A validated dynamic, computer-controlled in vitro system simulating the conditions in the proximal large intestine (TIM-2) was used. Sodium hydroxide (NaOH) consumption in the system was used as an indicator of fermentability and SCFA and branched chain fatty acids (BCFA) production was determined. NaOH consumption was significantly higher for Fructooligosaccharide (FOS) than PGX, which was higher than cellulose (p = 0.002). At 32, 48 and 72 h, acetate and butyrate production were higher for FOS and PGX versus cellulose. Propionate production was higher for PGX than cellulose at 32, 48, 56 and 72 h and higher than FOS at 72 h (p = 0.014). Total BCFA production was lower for FOS compared to cellulose, whereas production with PGX was lower than for cellulose at 72 h. In conclusion, PGX is fermented by the colonic microbiota which appeared to adapt to the substrate over time. The greater propionate production for PGX may explain part of the cholesterol-lowering properties of PGX seen in rodents and humans. MDPI 2014-03-14 /pmc/articles/PMC3967181/ /pubmed/24638070 http://dx.doi.org/10.3390/nu6031115 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Reimer, Raylene A.
Maathuis, Annet J. H.
Venema, Koen
Lyon, Michael R.
Gahler, Roland J.
Wood, Simon
Effect of the Novel Polysaccharide PolyGlycopleX(®) on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large Intestine
title Effect of the Novel Polysaccharide PolyGlycopleX(®) on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large Intestine
title_full Effect of the Novel Polysaccharide PolyGlycopleX(®) on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large Intestine
title_fullStr Effect of the Novel Polysaccharide PolyGlycopleX(®) on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large Intestine
title_full_unstemmed Effect of the Novel Polysaccharide PolyGlycopleX(®) on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large Intestine
title_short Effect of the Novel Polysaccharide PolyGlycopleX(®) on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large Intestine
title_sort effect of the novel polysaccharide polyglycoplex(®) on short-chain fatty acid production in a computer-controlled in vitro model of the human large intestine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967181/
https://www.ncbi.nlm.nih.gov/pubmed/24638070
http://dx.doi.org/10.3390/nu6031115
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