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Long term but not short term exposure to obesity related microbiota promotes host insulin resistance
The intestinal microbiota and insulin sensitivity are rapidly altered after ingestion of obesogenic diets. We find that changes in the composition of the fecal microbiota precede changes in glucose tolerance when mice are fed obesogenic, low fiber, high fat diets (HFDs). Antibiotics alter glycemia d...
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/PMC6224578/ https://www.ncbi.nlm.nih.gov/pubmed/30409977 http://dx.doi.org/10.1038/s41467-018-07146-5 |
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author | Foley, Kevin P. Zlitni, Soumaya Denou, Emmanuel Duggan, Brittany M. Chan, Rebecca W. Stearns, Jennifer C. Schertzer, Jonathan D. |
author_facet | Foley, Kevin P. Zlitni, Soumaya Denou, Emmanuel Duggan, Brittany M. Chan, Rebecca W. Stearns, Jennifer C. Schertzer, Jonathan D. |
author_sort | Foley, Kevin P. |
collection | PubMed |
description | The intestinal microbiota and insulin sensitivity are rapidly altered after ingestion of obesogenic diets. We find that changes in the composition of the fecal microbiota precede changes in glucose tolerance when mice are fed obesogenic, low fiber, high fat diets (HFDs). Antibiotics alter glycemia during the first week of certain HFDs, but antibiotics show a more robust improvement in glycemic control in mice with protracted obesity caused by long-term feeding of multiple HFDs. Microbiota transmissible dysglycemia and glucose intolerance only occur when germ-free mice are exposed to obesity-related microbes for more than 45 days. We find that sufficient host exposure time to microbiota derived from HFD-fed mice allows microbial factors to contribute to insulin resistance, independently from increased adiposity in mice. Our results are consistent with intestinal microbiota contributing to chronic insulin resistance and dysglycemia during prolonged obesity, despite rapid diet-induced changes in the taxonomic composition of the fecal microbiota. |
format | Online Article Text |
id | pubmed-6224578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62245782018-11-13 Long term but not short term exposure to obesity related microbiota promotes host insulin resistance Foley, Kevin P. Zlitni, Soumaya Denou, Emmanuel Duggan, Brittany M. Chan, Rebecca W. Stearns, Jennifer C. Schertzer, Jonathan D. Nat Commun Article The intestinal microbiota and insulin sensitivity are rapidly altered after ingestion of obesogenic diets. We find that changes in the composition of the fecal microbiota precede changes in glucose tolerance when mice are fed obesogenic, low fiber, high fat diets (HFDs). Antibiotics alter glycemia during the first week of certain HFDs, but antibiotics show a more robust improvement in glycemic control in mice with protracted obesity caused by long-term feeding of multiple HFDs. Microbiota transmissible dysglycemia and glucose intolerance only occur when germ-free mice are exposed to obesity-related microbes for more than 45 days. We find that sufficient host exposure time to microbiota derived from HFD-fed mice allows microbial factors to contribute to insulin resistance, independently from increased adiposity in mice. Our results are consistent with intestinal microbiota contributing to chronic insulin resistance and dysglycemia during prolonged obesity, despite rapid diet-induced changes in the taxonomic composition of the fecal microbiota. Nature Publishing Group UK 2018-11-08 /pmc/articles/PMC6224578/ /pubmed/30409977 http://dx.doi.org/10.1038/s41467-018-07146-5 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 Foley, Kevin P. Zlitni, Soumaya Denou, Emmanuel Duggan, Brittany M. Chan, Rebecca W. Stearns, Jennifer C. Schertzer, Jonathan D. Long term but not short term exposure to obesity related microbiota promotes host insulin resistance |
title | Long term but not short term exposure to obesity related microbiota promotes host insulin resistance |
title_full | Long term but not short term exposure to obesity related microbiota promotes host insulin resistance |
title_fullStr | Long term but not short term exposure to obesity related microbiota promotes host insulin resistance |
title_full_unstemmed | Long term but not short term exposure to obesity related microbiota promotes host insulin resistance |
title_short | Long term but not short term exposure to obesity related microbiota promotes host insulin resistance |
title_sort | long term but not short term exposure to obesity related microbiota promotes host insulin resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224578/ https://www.ncbi.nlm.nih.gov/pubmed/30409977 http://dx.doi.org/10.1038/s41467-018-07146-5 |
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