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Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes

Type 2 diabetes mellitus (T2DM), characterized by insulin resistance and unclear pathogenesis, is a serious menace to human health. Bile acids are the end products of cholesterol catabolism and play an important role in maintaining cholesterol homeostasis. Furthermore, increasing studies suggest tha...

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Detalles Bibliográficos
Autores principales: Wu, Yingjie, Zhou, An, Tang, Li, Lei, Yuanyuan, Tang, Bo, Zhang, Linjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383344/
https://www.ncbi.nlm.nih.gov/pubmed/32733968
http://dx.doi.org/10.1155/2020/6138438
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author Wu, Yingjie
Zhou, An
Tang, Li
Lei, Yuanyuan
Tang, Bo
Zhang, Linjing
author_facet Wu, Yingjie
Zhou, An
Tang, Li
Lei, Yuanyuan
Tang, Bo
Zhang, Linjing
author_sort Wu, Yingjie
collection PubMed
description Type 2 diabetes mellitus (T2DM), characterized by insulin resistance and unclear pathogenesis, is a serious menace to human health. Bile acids are the end products of cholesterol catabolism and play an important role in maintaining cholesterol homeostasis. Furthermore, increasing studies suggest that bile acids may regulate glucose tolerance, insulin sensitivity, and energy metabolism, suggesting that bile acids may represent a potential therapeutic target for T2DM. This study summarizes the metabolism of bile acids and, more importantly, changes in their concentrations, constitution, and receptors in diabetes. Furthermore, we provide an overview of the mechanisms underlying the role of bile acids in glucose and lipid metabolism, as well as the occurrence and development of T2DM. Bile acid-targeted therapy may represent a valid approach for T2DM treatment.
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spelling pubmed-73833442020-07-29 Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes Wu, Yingjie Zhou, An Tang, Li Lei, Yuanyuan Tang, Bo Zhang, Linjing J Diabetes Res Review Article Type 2 diabetes mellitus (T2DM), characterized by insulin resistance and unclear pathogenesis, is a serious menace to human health. Bile acids are the end products of cholesterol catabolism and play an important role in maintaining cholesterol homeostasis. Furthermore, increasing studies suggest that bile acids may regulate glucose tolerance, insulin sensitivity, and energy metabolism, suggesting that bile acids may represent a potential therapeutic target for T2DM. This study summarizes the metabolism of bile acids and, more importantly, changes in their concentrations, constitution, and receptors in diabetes. Furthermore, we provide an overview of the mechanisms underlying the role of bile acids in glucose and lipid metabolism, as well as the occurrence and development of T2DM. Bile acid-targeted therapy may represent a valid approach for T2DM treatment. Hindawi 2020-07-17 /pmc/articles/PMC7383344/ /pubmed/32733968 http://dx.doi.org/10.1155/2020/6138438 Text en Copyright © 2020 Yingjie Wu et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Wu, Yingjie
Zhou, An
Tang, Li
Lei, Yuanyuan
Tang, Bo
Zhang, Linjing
Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes
title Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes
title_full Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes
title_fullStr Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes
title_full_unstemmed Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes
title_short Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes
title_sort bile acids: key regulators and novel treatment targets for type 2 diabetes
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383344/
https://www.ncbi.nlm.nih.gov/pubmed/32733968
http://dx.doi.org/10.1155/2020/6138438
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