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Effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice
Dietary non-digestible carbohydrates are perceived to improve health via gut microbiota-dependent generation of products such as short-chain fatty acids (SCFA). In addition, SCFA are also precursors for lipid and cholesterol synthesis potentially resulting in unwanted effects on lipid metabolism. In...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125380/ https://www.ncbi.nlm.nih.gov/pubmed/30185894 http://dx.doi.org/10.1038/s41598-018-31698-7 |
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author | Mistry, Rima H. Gu, Fangjie Schols, Henk A. Verkade, Henkjan J. Tietge, Uwe J. F. |
author_facet | Mistry, Rima H. Gu, Fangjie Schols, Henk A. Verkade, Henkjan J. Tietge, Uwe J. F. |
author_sort | Mistry, Rima H. |
collection | PubMed |
description | Dietary non-digestible carbohydrates are perceived to improve health via gut microbiota-dependent generation of products such as short-chain fatty acids (SCFA). In addition, SCFA are also precursors for lipid and cholesterol synthesis potentially resulting in unwanted effects on lipid metabolism. Inulin is a widely used model prebiotic dietary fiber. Inconsistent reports on the effects of inulin on cholesterol homeostasis have emerged in humans and preclinical models. To clarify this issue, the present study aimed to provide an in-depth characterization of the effects of short-chain (sc)- and long-chain (lc)- inulin on cholesterol synthesis, absorption and elimination in mice. Feeding wildtype C57BL/6J mice diets supplemented with 10% (w/w) of either sc- or lc-inulin for two weeks resulted in approximately 2.5-fold higher fecal SCFA levels (P < 0.01) compared with controls, but had no significant effects on plasma and liver lipids. Subtle shifts in fecal and plasma bile acid species were detected with beta-muricholic acid increasing significantly in plasma of the inulin fed groups (1.7-fold, P < 0.05). However, neither sc-inulin nor lc-inulin affected intestinal cholesterol absorption, mass fecal cholesterol excretion or trans-intestinal cholesterol excretion (TICE). Combined, our data demonstrate that sc- and lc-inulin have no adverse effects on cholesterol metabolism in mice despite increased generation of SCFA. |
format | Online Article Text |
id | pubmed-6125380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61253802018-09-10 Effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice Mistry, Rima H. Gu, Fangjie Schols, Henk A. Verkade, Henkjan J. Tietge, Uwe J. F. Sci Rep Article Dietary non-digestible carbohydrates are perceived to improve health via gut microbiota-dependent generation of products such as short-chain fatty acids (SCFA). In addition, SCFA are also precursors for lipid and cholesterol synthesis potentially resulting in unwanted effects on lipid metabolism. Inulin is a widely used model prebiotic dietary fiber. Inconsistent reports on the effects of inulin on cholesterol homeostasis have emerged in humans and preclinical models. To clarify this issue, the present study aimed to provide an in-depth characterization of the effects of short-chain (sc)- and long-chain (lc)- inulin on cholesterol synthesis, absorption and elimination in mice. Feeding wildtype C57BL/6J mice diets supplemented with 10% (w/w) of either sc- or lc-inulin for two weeks resulted in approximately 2.5-fold higher fecal SCFA levels (P < 0.01) compared with controls, but had no significant effects on plasma and liver lipids. Subtle shifts in fecal and plasma bile acid species were detected with beta-muricholic acid increasing significantly in plasma of the inulin fed groups (1.7-fold, P < 0.05). However, neither sc-inulin nor lc-inulin affected intestinal cholesterol absorption, mass fecal cholesterol excretion or trans-intestinal cholesterol excretion (TICE). Combined, our data demonstrate that sc- and lc-inulin have no adverse effects on cholesterol metabolism in mice despite increased generation of SCFA. Nature Publishing Group UK 2018-09-05 /pmc/articles/PMC6125380/ /pubmed/30185894 http://dx.doi.org/10.1038/s41598-018-31698-7 Text en © The Author(s) 2018 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 Mistry, Rima H. Gu, Fangjie Schols, Henk A. Verkade, Henkjan J. Tietge, Uwe J. F. Effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice |
title | Effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice |
title_full | Effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice |
title_fullStr | Effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice |
title_full_unstemmed | Effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice |
title_short | Effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice |
title_sort | effect of the prebiotic fiber inulin on cholesterol metabolism in wildtype mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125380/ https://www.ncbi.nlm.nih.gov/pubmed/30185894 http://dx.doi.org/10.1038/s41598-018-31698-7 |
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