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Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet

SCOPE: The gut microbiota might critically modify metabolic disease development. Dietary fibers such as galacto‐oligosaccharides (GOS) presumably stimulate bacteria beneficial for metabolic health. This study assesses the impact of GOS on obesity, glucose, and lipid metabolism. METHODS AND RESULTS:...

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Autores principales: Mistry, Rima H., Liu, Fan, Borewicz, Klaudyna, Lohuis, Mirjam A. M., Smidt, Hauke, Verkade, Henkjan J., Tietge, Uwe J. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379190/
https://www.ncbi.nlm.nih.gov/pubmed/32380577
http://dx.doi.org/10.1002/mnfr.201900922
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author Mistry, Rima H.
Liu, Fan
Borewicz, Klaudyna
Lohuis, Mirjam A. M.
Smidt, Hauke
Verkade, Henkjan J.
Tietge, Uwe J. F.
author_facet Mistry, Rima H.
Liu, Fan
Borewicz, Klaudyna
Lohuis, Mirjam A. M.
Smidt, Hauke
Verkade, Henkjan J.
Tietge, Uwe J. F.
author_sort Mistry, Rima H.
collection PubMed
description SCOPE: The gut microbiota might critically modify metabolic disease development. Dietary fibers such as galacto‐oligosaccharides (GOS) presumably stimulate bacteria beneficial for metabolic health. This study assesses the impact of GOS on obesity, glucose, and lipid metabolism. METHODS AND RESULTS: Following Western‐type diet feeding (C57BL/6 mice) with or without β‐GOS (7% w/w, 15 weeks), body composition, glucose and insulin tolerance, lipid profiles, fat kinetics and microbiota composition are analyzed. GOS reduces body weight gain (p < 0.01), accumulation of epididymal (p < 0.05), perirenal (p < 0.01) fat, and insulin resistance (p < 0.01). GOS‐fed mice have lower plasma cholesterol (p < 0.05), mainly within low‐density lipoproteins, lower intestinal fat absorption (p < 0.01), more fecal neutral sterol excretion (p < 0.05) and higher intestinal GLP‐1 expression (p < 0.01). Fecal bile acid excretion is lower (p < 0.01) in GOS‐fed mice with significant compositional differences, namely decreased cholic, α‐muricholic, and deoxycholic acid excretion, whereas hyodeoxycholic acid increased. Substantial changes in microbiota composition, conceivably beneficial for metabolic health, occurred upon GOS feeding. CONCLUSION: GOS supplementation to a Western‐type diet improves body weight gain, dyslipidemia, and insulin sensitivity, supporting a therapeutic potential of GOS for individuals at risk of developing metabolic syndrome.
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spelling pubmed-73791902020-07-24 Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet Mistry, Rima H. Liu, Fan Borewicz, Klaudyna Lohuis, Mirjam A. M. Smidt, Hauke Verkade, Henkjan J. Tietge, Uwe J. F. Mol Nutr Food Res Research Articles SCOPE: The gut microbiota might critically modify metabolic disease development. Dietary fibers such as galacto‐oligosaccharides (GOS) presumably stimulate bacteria beneficial for metabolic health. This study assesses the impact of GOS on obesity, glucose, and lipid metabolism. METHODS AND RESULTS: Following Western‐type diet feeding (C57BL/6 mice) with or without β‐GOS (7% w/w, 15 weeks), body composition, glucose and insulin tolerance, lipid profiles, fat kinetics and microbiota composition are analyzed. GOS reduces body weight gain (p < 0.01), accumulation of epididymal (p < 0.05), perirenal (p < 0.01) fat, and insulin resistance (p < 0.01). GOS‐fed mice have lower plasma cholesterol (p < 0.05), mainly within low‐density lipoproteins, lower intestinal fat absorption (p < 0.01), more fecal neutral sterol excretion (p < 0.05) and higher intestinal GLP‐1 expression (p < 0.01). Fecal bile acid excretion is lower (p < 0.01) in GOS‐fed mice with significant compositional differences, namely decreased cholic, α‐muricholic, and deoxycholic acid excretion, whereas hyodeoxycholic acid increased. Substantial changes in microbiota composition, conceivably beneficial for metabolic health, occurred upon GOS feeding. CONCLUSION: GOS supplementation to a Western‐type diet improves body weight gain, dyslipidemia, and insulin sensitivity, supporting a therapeutic potential of GOS for individuals at risk of developing metabolic syndrome. John Wiley and Sons Inc. 2020-05-25 2020-06 /pmc/articles/PMC7379190/ /pubmed/32380577 http://dx.doi.org/10.1002/mnfr.201900922 Text en © 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Mistry, Rima H.
Liu, Fan
Borewicz, Klaudyna
Lohuis, Mirjam A. M.
Smidt, Hauke
Verkade, Henkjan J.
Tietge, Uwe J. F.
Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet
title Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet
title_full Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet
title_fullStr Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet
title_full_unstemmed Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet
title_short Long‐Term β‐galacto‐oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western‐Type Diet
title_sort long‐term β‐galacto‐oligosaccharides supplementation decreases the development of obesity and insulin resistance in mice fed a western‐type diet
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379190/
https://www.ncbi.nlm.nih.gov/pubmed/32380577
http://dx.doi.org/10.1002/mnfr.201900922
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