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Bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus
Type 2 diabetes mellitus (T2DM) occurs that cannot effectively use the insulin. Insulin Resistance (IR) is a significant characteristic of T2DM which is also an essential treatment target in blood glucose regulation to prevent T2DM and its complications. Bile acids (BAs) are one group of bioactive m...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640995/ https://www.ncbi.nlm.nih.gov/pubmed/36386219 http://dx.doi.org/10.3389/fphar.2022.1027212 |
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author | Gao, Ruolin Meng, Xiangjing Xue, Yili Mao, Min Liu, Yaru Tian, Xuewen Sui, Bo Li, Xun Zhang, Pengyi |
author_facet | Gao, Ruolin Meng, Xiangjing Xue, Yili Mao, Min Liu, Yaru Tian, Xuewen Sui, Bo Li, Xun Zhang, Pengyi |
author_sort | Gao, Ruolin |
collection | PubMed |
description | Type 2 diabetes mellitus (T2DM) occurs that cannot effectively use the insulin. Insulin Resistance (IR) is a significant characteristic of T2DM which is also an essential treatment target in blood glucose regulation to prevent T2DM and its complications. Bile acids (BAs) are one group of bioactive metabolites synthesized from cholesterol in liver. BAs play an important role in mutualistic symbiosis between host and gut microbiota. It is shown that T2DM is associated with altered bile acid metabolism which can be regulated by gut microbiota. Simultaneously, BAs also reshape gut microbiota and improve IR and T2DM in the bidirectional communications of the gut-liver axis. This article reviewed the findings on the interaction between BAs and gut microbiota in improving T2DM, which focused on gut microbiota and its debinding function and BAs regulated gut microbiota through FXR/TGR5. Meanwhile, BAs and their derivatives that are effective for improving T2DM and other treatments based on bile acid metabolism were also summarized. This review highlighted that BAs play a critical role in the glucose metabolism and may serve as therapeutic targets in T2DM, providing a reference for discovering and screening novel therapeutic drugs. |
format | Online Article Text |
id | pubmed-9640995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96409952022-11-15 Bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus Gao, Ruolin Meng, Xiangjing Xue, Yili Mao, Min Liu, Yaru Tian, Xuewen Sui, Bo Li, Xun Zhang, Pengyi Front Pharmacol Pharmacology Type 2 diabetes mellitus (T2DM) occurs that cannot effectively use the insulin. Insulin Resistance (IR) is a significant characteristic of T2DM which is also an essential treatment target in blood glucose regulation to prevent T2DM and its complications. Bile acids (BAs) are one group of bioactive metabolites synthesized from cholesterol in liver. BAs play an important role in mutualistic symbiosis between host and gut microbiota. It is shown that T2DM is associated with altered bile acid metabolism which can be regulated by gut microbiota. Simultaneously, BAs also reshape gut microbiota and improve IR and T2DM in the bidirectional communications of the gut-liver axis. This article reviewed the findings on the interaction between BAs and gut microbiota in improving T2DM, which focused on gut microbiota and its debinding function and BAs regulated gut microbiota through FXR/TGR5. Meanwhile, BAs and their derivatives that are effective for improving T2DM and other treatments based on bile acid metabolism were also summarized. This review highlighted that BAs play a critical role in the glucose metabolism and may serve as therapeutic targets in T2DM, providing a reference for discovering and screening novel therapeutic drugs. Frontiers Media S.A. 2022-10-25 /pmc/articles/PMC9640995/ /pubmed/36386219 http://dx.doi.org/10.3389/fphar.2022.1027212 Text en Copyright © 2022 Gao, Meng, Xue, Mao, Liu, Tian, Sui, Li and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Gao, Ruolin Meng, Xiangjing Xue, Yili Mao, Min Liu, Yaru Tian, Xuewen Sui, Bo Li, Xun Zhang, Pengyi Bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus |
title | Bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus |
title_full | Bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus |
title_fullStr | Bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus |
title_full_unstemmed | Bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus |
title_short | Bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus |
title_sort | bile acids-gut microbiota crosstalk contributes to the improvement of type 2 diabetes mellitus |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640995/ https://www.ncbi.nlm.nih.gov/pubmed/36386219 http://dx.doi.org/10.3389/fphar.2022.1027212 |
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