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The anti-cholesterolaemic effect of a consortium of probiotics: An acute study in C57BL/6J mice
Hypercholesterolaemia is a major risk factor for cardiovascular disease and it has been found that some probiotic bacteria possess cholesterol-lowering capabilities. In this study, the ability of the Lab4 probiotic consortium to hydrolyse bile salts, assimilate cholesterol and regulate cholesterol t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460276/ https://www.ncbi.nlm.nih.gov/pubmed/28588193 http://dx.doi.org/10.1038/s41598-017-02889-5 |
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author | Michael, D. R. Davies, T. S. Moss, J. W. E. Calvente, D. Lama Ramji, D. P. Marchesi, J. R. Pechlivanis, A. Plummer, S. F. Hughes, T. R. |
author_facet | Michael, D. R. Davies, T. S. Moss, J. W. E. Calvente, D. Lama Ramji, D. P. Marchesi, J. R. Pechlivanis, A. Plummer, S. F. Hughes, T. R. |
author_sort | Michael, D. R. |
collection | PubMed |
description | Hypercholesterolaemia is a major risk factor for cardiovascular disease and it has been found that some probiotic bacteria possess cholesterol-lowering capabilities. In this study, the ability of the Lab4 probiotic consortium to hydrolyse bile salts, assimilate cholesterol and regulate cholesterol transport by polarised Caco-2 enterocytes was demonstrated. Furthermore, in wild-type C57BL/6J mice fed a high fat diet, 2-weeks supplementation with Lab4 probiotic consortium plus Lactobacillus plantarum CUL66 resulted in significant reductions in plasma total cholesterol levels and suppression of diet-induced weight gain. No changes in plasma levels of very low-density lipoprotein/low-density lipoprotein, high-density lipoprotein, triglycerides, cytokines or bile acids were observed. Increased amounts of total and unconjugated bile acids in the faeces of the probiotic-fed mice, together with modulation of hepatic small heterodimer partner and cholesterol-7α-hydroxylase mRNA expression, implicates bile salt hydrolase activity as a potential mechanism of action. In summary, this study demonstrates the cholesterol-lowering efficacy of short-term feeding of the Lab4 probiotic consortium plus L. plantarum CUL66 in wild-type mice and supports further assessment in human trials. |
format | Online Article Text |
id | pubmed-5460276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54602762017-06-07 The anti-cholesterolaemic effect of a consortium of probiotics: An acute study in C57BL/6J mice Michael, D. R. Davies, T. S. Moss, J. W. E. Calvente, D. Lama Ramji, D. P. Marchesi, J. R. Pechlivanis, A. Plummer, S. F. Hughes, T. R. Sci Rep Article Hypercholesterolaemia is a major risk factor for cardiovascular disease and it has been found that some probiotic bacteria possess cholesterol-lowering capabilities. In this study, the ability of the Lab4 probiotic consortium to hydrolyse bile salts, assimilate cholesterol and regulate cholesterol transport by polarised Caco-2 enterocytes was demonstrated. Furthermore, in wild-type C57BL/6J mice fed a high fat diet, 2-weeks supplementation with Lab4 probiotic consortium plus Lactobacillus plantarum CUL66 resulted in significant reductions in plasma total cholesterol levels and suppression of diet-induced weight gain. No changes in plasma levels of very low-density lipoprotein/low-density lipoprotein, high-density lipoprotein, triglycerides, cytokines or bile acids were observed. Increased amounts of total and unconjugated bile acids in the faeces of the probiotic-fed mice, together with modulation of hepatic small heterodimer partner and cholesterol-7α-hydroxylase mRNA expression, implicates bile salt hydrolase activity as a potential mechanism of action. In summary, this study demonstrates the cholesterol-lowering efficacy of short-term feeding of the Lab4 probiotic consortium plus L. plantarum CUL66 in wild-type mice and supports further assessment in human trials. Nature Publishing Group UK 2017-06-06 /pmc/articles/PMC5460276/ /pubmed/28588193 http://dx.doi.org/10.1038/s41598-017-02889-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Michael, D. R. Davies, T. S. Moss, J. W. E. Calvente, D. Lama Ramji, D. P. Marchesi, J. R. Pechlivanis, A. Plummer, S. F. Hughes, T. R. The anti-cholesterolaemic effect of a consortium of probiotics: An acute study in C57BL/6J mice |
title | The anti-cholesterolaemic effect of a consortium of probiotics: An acute study in C57BL/6J mice |
title_full | The anti-cholesterolaemic effect of a consortium of probiotics: An acute study in C57BL/6J mice |
title_fullStr | The anti-cholesterolaemic effect of a consortium of probiotics: An acute study in C57BL/6J mice |
title_full_unstemmed | The anti-cholesterolaemic effect of a consortium of probiotics: An acute study in C57BL/6J mice |
title_short | The anti-cholesterolaemic effect of a consortium of probiotics: An acute study in C57BL/6J mice |
title_sort | anti-cholesterolaemic effect of a consortium of probiotics: an acute study in c57bl/6j mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460276/ https://www.ncbi.nlm.nih.gov/pubmed/28588193 http://dx.doi.org/10.1038/s41598-017-02889-5 |
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