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Parabacteroides distasonis ameliorates insulin resistance via activation of intestinal GPR109a

Gut microbiota plays a key role in insulin resistance (IR). Here we perform a case-control study of Chinese adults (ChiCTR2200065715) and identify that Parabacteroides distasonis is inversely correlated with IR. Treatment with P. distasonis improves IR, strengthens intestinal integrity, and reduces...

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Autores principales: Sun, Yonggan, Nie, Qixing, Zhang, Shanshan, He, Huijun, Zuo, Sheng, Chen, Chunhua, Yang, Jingrui, Chen, Haihong, Hu, Jielun, Li, Song, Cheng, Jiaobo, Zhang, Baojie, Zheng, Zhitian, Pan, Shijie, Huang, Ping, Lian, Lu, Nie, Shaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676405/
https://www.ncbi.nlm.nih.gov/pubmed/38007572
http://dx.doi.org/10.1038/s41467-023-43622-3
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author Sun, Yonggan
Nie, Qixing
Zhang, Shanshan
He, Huijun
Zuo, Sheng
Chen, Chunhua
Yang, Jingrui
Chen, Haihong
Hu, Jielun
Li, Song
Cheng, Jiaobo
Zhang, Baojie
Zheng, Zhitian
Pan, Shijie
Huang, Ping
Lian, Lu
Nie, Shaoping
author_facet Sun, Yonggan
Nie, Qixing
Zhang, Shanshan
He, Huijun
Zuo, Sheng
Chen, Chunhua
Yang, Jingrui
Chen, Haihong
Hu, Jielun
Li, Song
Cheng, Jiaobo
Zhang, Baojie
Zheng, Zhitian
Pan, Shijie
Huang, Ping
Lian, Lu
Nie, Shaoping
author_sort Sun, Yonggan
collection PubMed
description Gut microbiota plays a key role in insulin resistance (IR). Here we perform a case-control study of Chinese adults (ChiCTR2200065715) and identify that Parabacteroides distasonis is inversely correlated with IR. Treatment with P. distasonis improves IR, strengthens intestinal integrity, and reduces systemic inflammation in mice. We further demonstrate that P. distasonis-derived nicotinic acid (NA) is a vital bioactive molecule that fortifies intestinal barrier function via activating intestinal G-protein-coupled receptor 109a (GPR109a), leading to ameliorating IR. We also conduct a bioactive dietary fiber screening to induce P. distasonis growth. Dendrobium officinale polysaccharide (DOP) shows favorable growth-promoting effects on P. distasonis and protects against IR in mice simultaneously. Finally, the reduced P. distasonis and NA levels were also validated in another human type 2 diabetes mellitus cohort. These findings reveal the unique mechanisms of P. distasonis on IR and provide viable strategies for the treatment and prevention of IR by bioactive dietary fiber.
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spelling pubmed-106764052023-11-25 Parabacteroides distasonis ameliorates insulin resistance via activation of intestinal GPR109a Sun, Yonggan Nie, Qixing Zhang, Shanshan He, Huijun Zuo, Sheng Chen, Chunhua Yang, Jingrui Chen, Haihong Hu, Jielun Li, Song Cheng, Jiaobo Zhang, Baojie Zheng, Zhitian Pan, Shijie Huang, Ping Lian, Lu Nie, Shaoping Nat Commun Article Gut microbiota plays a key role in insulin resistance (IR). Here we perform a case-control study of Chinese adults (ChiCTR2200065715) and identify that Parabacteroides distasonis is inversely correlated with IR. Treatment with P. distasonis improves IR, strengthens intestinal integrity, and reduces systemic inflammation in mice. We further demonstrate that P. distasonis-derived nicotinic acid (NA) is a vital bioactive molecule that fortifies intestinal barrier function via activating intestinal G-protein-coupled receptor 109a (GPR109a), leading to ameliorating IR. We also conduct a bioactive dietary fiber screening to induce P. distasonis growth. Dendrobium officinale polysaccharide (DOP) shows favorable growth-promoting effects on P. distasonis and protects against IR in mice simultaneously. Finally, the reduced P. distasonis and NA levels were also validated in another human type 2 diabetes mellitus cohort. These findings reveal the unique mechanisms of P. distasonis on IR and provide viable strategies for the treatment and prevention of IR by bioactive dietary fiber. Nature Publishing Group UK 2023-11-25 /pmc/articles/PMC10676405/ /pubmed/38007572 http://dx.doi.org/10.1038/s41467-023-43622-3 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sun, Yonggan
Nie, Qixing
Zhang, Shanshan
He, Huijun
Zuo, Sheng
Chen, Chunhua
Yang, Jingrui
Chen, Haihong
Hu, Jielun
Li, Song
Cheng, Jiaobo
Zhang, Baojie
Zheng, Zhitian
Pan, Shijie
Huang, Ping
Lian, Lu
Nie, Shaoping
Parabacteroides distasonis ameliorates insulin resistance via activation of intestinal GPR109a
title Parabacteroides distasonis ameliorates insulin resistance via activation of intestinal GPR109a
title_full Parabacteroides distasonis ameliorates insulin resistance via activation of intestinal GPR109a
title_fullStr Parabacteroides distasonis ameliorates insulin resistance via activation of intestinal GPR109a
title_full_unstemmed Parabacteroides distasonis ameliorates insulin resistance via activation of intestinal GPR109a
title_short Parabacteroides distasonis ameliorates insulin resistance via activation of intestinal GPR109a
title_sort parabacteroides distasonis ameliorates insulin resistance via activation of intestinal gpr109a
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676405/
https://www.ncbi.nlm.nih.gov/pubmed/38007572
http://dx.doi.org/10.1038/s41467-023-43622-3
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