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High-cholesterol diet does not alter gut microbiota composition in mice

INTRODUCTION: Western diet containing both saturated fat and cholesterol impairs cardio-metabolic health partly by modulating diversity and function of the microbiota. While diet containing only high fat has comparable effects, it is unclear how diets only enriched in cholesterol impact the microbio...

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Autores principales: Dimova, Lidiya G., Zlatkov, Nikola, Verkade, Henkjan J., Uhlin, Bernt Eric, Tietge, Uwe J. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314487/
https://www.ncbi.nlm.nih.gov/pubmed/28239402
http://dx.doi.org/10.1186/s12986-017-0170-x
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author Dimova, Lidiya G.
Zlatkov, Nikola
Verkade, Henkjan J.
Uhlin, Bernt Eric
Tietge, Uwe J. F.
author_facet Dimova, Lidiya G.
Zlatkov, Nikola
Verkade, Henkjan J.
Uhlin, Bernt Eric
Tietge, Uwe J. F.
author_sort Dimova, Lidiya G.
collection PubMed
description INTRODUCTION: Western diet containing both saturated fat and cholesterol impairs cardio-metabolic health partly by modulating diversity and function of the microbiota. While diet containing only high fat has comparable effects, it is unclear how diets only enriched in cholesterol impact the microbiota. Therefore, we aimed to characterize the response of host and microbiota to a high cholesterol (HC) diet in mice susceptible to cardio-metabolic disease. METHODS: LDLR knockout mice received either 1.25% HC or no cholesterol containing control diet (NC) for 12 weeks before characterizing host cholesterol metabolism and intestinal microbiota composition (next generation sequencing). RESULTS: HC diet substantially increased plasma (1.6-fold) and liver cholesterol levels (21-fold), biliary cholesterol secretion (4.5-fold) and fecal neutral sterol excretion (68-fold, each p < 0.001) but not fecal bile acid excretion. Interestingly, despite the profound changes in intestinal cholesterol homeostasis no differences in microbial composition between control and HC-fed mice were detected. In both groups the main phyla were Bacteroidetes (55%), Firmicutes (27%) and Verrucomicrobia (14%). CONCLUSION: Our results demonstrate that in mice HC diet alone does not alter the microbiota composition despite inducing substantial adaptive changes in whole body cholesterol homeostasis. The impact of Western diet on intestinal microbiota thus appears to be mediated exclusively by its high fat content. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12986-017-0170-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-53144872017-02-24 High-cholesterol diet does not alter gut microbiota composition in mice Dimova, Lidiya G. Zlatkov, Nikola Verkade, Henkjan J. Uhlin, Bernt Eric Tietge, Uwe J. F. Nutr Metab (Lond) Brief Communication INTRODUCTION: Western diet containing both saturated fat and cholesterol impairs cardio-metabolic health partly by modulating diversity and function of the microbiota. While diet containing only high fat has comparable effects, it is unclear how diets only enriched in cholesterol impact the microbiota. Therefore, we aimed to characterize the response of host and microbiota to a high cholesterol (HC) diet in mice susceptible to cardio-metabolic disease. METHODS: LDLR knockout mice received either 1.25% HC or no cholesterol containing control diet (NC) for 12 weeks before characterizing host cholesterol metabolism and intestinal microbiota composition (next generation sequencing). RESULTS: HC diet substantially increased plasma (1.6-fold) and liver cholesterol levels (21-fold), biliary cholesterol secretion (4.5-fold) and fecal neutral sterol excretion (68-fold, each p < 0.001) but not fecal bile acid excretion. Interestingly, despite the profound changes in intestinal cholesterol homeostasis no differences in microbial composition between control and HC-fed mice were detected. In both groups the main phyla were Bacteroidetes (55%), Firmicutes (27%) and Verrucomicrobia (14%). CONCLUSION: Our results demonstrate that in mice HC diet alone does not alter the microbiota composition despite inducing substantial adaptive changes in whole body cholesterol homeostasis. The impact of Western diet on intestinal microbiota thus appears to be mediated exclusively by its high fat content. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12986-017-0170-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-16 /pmc/articles/PMC5314487/ /pubmed/28239402 http://dx.doi.org/10.1186/s12986-017-0170-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Brief Communication
Dimova, Lidiya G.
Zlatkov, Nikola
Verkade, Henkjan J.
Uhlin, Bernt Eric
Tietge, Uwe J. F.
High-cholesterol diet does not alter gut microbiota composition in mice
title High-cholesterol diet does not alter gut microbiota composition in mice
title_full High-cholesterol diet does not alter gut microbiota composition in mice
title_fullStr High-cholesterol diet does not alter gut microbiota composition in mice
title_full_unstemmed High-cholesterol diet does not alter gut microbiota composition in mice
title_short High-cholesterol diet does not alter gut microbiota composition in mice
title_sort high-cholesterol diet does not alter gut microbiota composition in mice
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314487/
https://www.ncbi.nlm.nih.gov/pubmed/28239402
http://dx.doi.org/10.1186/s12986-017-0170-x
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