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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...

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Autores principales: Gao, Ruolin, Meng, Xiangjing, Xue, Yili, Mao, Min, Liu, Yaru, Tian, Xuewen, Sui, Bo, Li, Xun, Zhang, Pengyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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.
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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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