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Gut microbial carbohydrate metabolism contributes to insulin resistance
Insulin resistance is the primary pathophysiology underlying metabolic syndrome and type 2 diabetes(1,2). Previous metagenomic studies have described the characteristics of gut microbiota and their roles in metabolizing major nutrients in insulin resistance(3–9). In particular, carbohydrate metaboli...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499599/ https://www.ncbi.nlm.nih.gov/pubmed/37648852 http://dx.doi.org/10.1038/s41586-023-06466-x |
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author | Takeuchi, Tadashi Kubota, Tetsuya Nakanishi, Yumiko Tsugawa, Hiroshi Suda, Wataru Kwon, Andrew Tae-Jun Yazaki, Junshi Ikeda, Kazutaka Nemoto, Shino Mochizuki, Yoshiki Kitami, Toshimori Yugi, Katsuyuki Mizuno, Yoshiko Yamamichi, Nobutake Yamazaki, Tsutomu Takamoto, Iseki Kubota, Naoto Kadowaki, Takashi Arner, Erik Carninci, Piero Ohara, Osamu Arita, Makoto Hattori, Masahira Koyasu, Shigeo Ohno, Hiroshi |
author_facet | Takeuchi, Tadashi Kubota, Tetsuya Nakanishi, Yumiko Tsugawa, Hiroshi Suda, Wataru Kwon, Andrew Tae-Jun Yazaki, Junshi Ikeda, Kazutaka Nemoto, Shino Mochizuki, Yoshiki Kitami, Toshimori Yugi, Katsuyuki Mizuno, Yoshiko Yamamichi, Nobutake Yamazaki, Tsutomu Takamoto, Iseki Kubota, Naoto Kadowaki, Takashi Arner, Erik Carninci, Piero Ohara, Osamu Arita, Makoto Hattori, Masahira Koyasu, Shigeo Ohno, Hiroshi |
author_sort | Takeuchi, Tadashi |
collection | PubMed |
description | Insulin resistance is the primary pathophysiology underlying metabolic syndrome and type 2 diabetes(1,2). Previous metagenomic studies have described the characteristics of gut microbiota and their roles in metabolizing major nutrients in insulin resistance(3–9). In particular, carbohydrate metabolism of commensals has been proposed to contribute up to 10% of the host’s overall energy extraction(10), thereby playing a role in the pathogenesis of obesity and prediabetes(3,4,6). Nevertheless, the underlying mechanism remains unclear. Here we investigate this relationship using a comprehensive multi-omics strategy in humans. We combine unbiased faecal metabolomics with metagenomics, host metabolomics and transcriptomics data to profile the involvement of the microbiome in insulin resistance. These data reveal that faecal carbohydrates, particularly host-accessible monosaccharides, are increased in individuals with insulin resistance and are associated with microbial carbohydrate metabolisms and host inflammatory cytokines. We identify gut bacteria associated with insulin resistance and insulin sensitivity that show a distinct pattern of carbohydrate metabolism, and demonstrate that insulin-sensitivity-associated bacteria ameliorate host phenotypes of insulin resistance in a mouse model. Our study, which provides a comprehensive view of the host–microorganism relationships in insulin resistance, reveals the impact of carbohydrate metabolism by microbiota, suggesting a potential therapeutic target for ameliorating insulin resistance. |
format | Online Article Text |
id | pubmed-10499599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104995992023-09-15 Gut microbial carbohydrate metabolism contributes to insulin resistance Takeuchi, Tadashi Kubota, Tetsuya Nakanishi, Yumiko Tsugawa, Hiroshi Suda, Wataru Kwon, Andrew Tae-Jun Yazaki, Junshi Ikeda, Kazutaka Nemoto, Shino Mochizuki, Yoshiki Kitami, Toshimori Yugi, Katsuyuki Mizuno, Yoshiko Yamamichi, Nobutake Yamazaki, Tsutomu Takamoto, Iseki Kubota, Naoto Kadowaki, Takashi Arner, Erik Carninci, Piero Ohara, Osamu Arita, Makoto Hattori, Masahira Koyasu, Shigeo Ohno, Hiroshi Nature Article Insulin resistance is the primary pathophysiology underlying metabolic syndrome and type 2 diabetes(1,2). Previous metagenomic studies have described the characteristics of gut microbiota and their roles in metabolizing major nutrients in insulin resistance(3–9). In particular, carbohydrate metabolism of commensals has been proposed to contribute up to 10% of the host’s overall energy extraction(10), thereby playing a role in the pathogenesis of obesity and prediabetes(3,4,6). Nevertheless, the underlying mechanism remains unclear. Here we investigate this relationship using a comprehensive multi-omics strategy in humans. We combine unbiased faecal metabolomics with metagenomics, host metabolomics and transcriptomics data to profile the involvement of the microbiome in insulin resistance. These data reveal that faecal carbohydrates, particularly host-accessible monosaccharides, are increased in individuals with insulin resistance and are associated with microbial carbohydrate metabolisms and host inflammatory cytokines. We identify gut bacteria associated with insulin resistance and insulin sensitivity that show a distinct pattern of carbohydrate metabolism, and demonstrate that insulin-sensitivity-associated bacteria ameliorate host phenotypes of insulin resistance in a mouse model. Our study, which provides a comprehensive view of the host–microorganism relationships in insulin resistance, reveals the impact of carbohydrate metabolism by microbiota, suggesting a potential therapeutic target for ameliorating insulin resistance. Nature Publishing Group UK 2023-08-30 2023 /pmc/articles/PMC10499599/ /pubmed/37648852 http://dx.doi.org/10.1038/s41586-023-06466-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Takeuchi, Tadashi Kubota, Tetsuya Nakanishi, Yumiko Tsugawa, Hiroshi Suda, Wataru Kwon, Andrew Tae-Jun Yazaki, Junshi Ikeda, Kazutaka Nemoto, Shino Mochizuki, Yoshiki Kitami, Toshimori Yugi, Katsuyuki Mizuno, Yoshiko Yamamichi, Nobutake Yamazaki, Tsutomu Takamoto, Iseki Kubota, Naoto Kadowaki, Takashi Arner, Erik Carninci, Piero Ohara, Osamu Arita, Makoto Hattori, Masahira Koyasu, Shigeo Ohno, Hiroshi Gut microbial carbohydrate metabolism contributes to insulin resistance |
title | Gut microbial carbohydrate metabolism contributes to insulin resistance |
title_full | Gut microbial carbohydrate metabolism contributes to insulin resistance |
title_fullStr | Gut microbial carbohydrate metabolism contributes to insulin resistance |
title_full_unstemmed | Gut microbial carbohydrate metabolism contributes to insulin resistance |
title_short | Gut microbial carbohydrate metabolism contributes to insulin resistance |
title_sort | gut microbial carbohydrate metabolism contributes to insulin resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499599/ https://www.ncbi.nlm.nih.gov/pubmed/37648852 http://dx.doi.org/10.1038/s41586-023-06466-x |
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