Bile acid metabolism and signaling in liver disease and therapy

Bile acids play a critical role in the regulation of glucose, lipid, and energy metabolism through activation of the nuclear bile acid receptor farnesoid X receptor (FXR) and membrane G protein-coupled bile acid receptor-1 (Gpbar-1, aka TGR5). Agonist activation of FXR and TGR5 improves insulin and...

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Main Author: John Y.L. Chiang
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2017-06-01
Series:Liver Research
Online Access:http://www.sciencedirect.com/science/article/pii/S2542568417000071
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spelling doaj-d1541a2a6c024be88b87a27f79976b7a2021-03-02T10:37:01ZengKeAi Communications Co., Ltd.Liver Research2542-56842017-06-011139Bile acid metabolism and signaling in liver disease and therapyJohn Y.L. Chiang0Department of Integrative Medical Sciences, College of Medicine, Northeast Ohio Medical University, Rootstown, OH, USABile acids play a critical role in the regulation of glucose, lipid, and energy metabolism through activation of the nuclear bile acid receptor farnesoid X receptor (FXR) and membrane G protein-coupled bile acid receptor-1 (Gpbar-1, aka TGR5). Agonist activation of FXR and TGR5 improves insulin and glucose sensitivity and stimulates energy metabolism to prevent diabetes, obesity, and non-alcoholic fatty liver disease (NAFLD). Bile acids have both pro- and anti-inflammatory actions through FXR and TGR5 in the intestine and liver. In the intestine, bile acids activate FXR and TGR5 to stimulate fibroblast growth factor 15 and glucagon-like peptide-1 secretion. FXR and TGR5 agonists may have therapeutic potential for treating liver-related metabolic diseases, such as diabetes and NAFLD. Keywords: Bile acid metabolism, Cholestatic liver diseases, Metabolic diseaseshttp://www.sciencedirect.com/science/article/pii/S2542568417000071
collection DOAJ
language English
format Article
sources DOAJ
author John Y.L. Chiang
spellingShingle John Y.L. Chiang
Bile acid metabolism and signaling in liver disease and therapy
Liver Research
author_facet John Y.L. Chiang
author_sort John Y.L. Chiang
title Bile acid metabolism and signaling in liver disease and therapy
title_short Bile acid metabolism and signaling in liver disease and therapy
title_full Bile acid metabolism and signaling in liver disease and therapy
title_fullStr Bile acid metabolism and signaling in liver disease and therapy
title_full_unstemmed Bile acid metabolism and signaling in liver disease and therapy
title_sort bile acid metabolism and signaling in liver disease and therapy
publisher KeAi Communications Co., Ltd.
series Liver Research
issn 2542-5684
publishDate 2017-06-01
description Bile acids play a critical role in the regulation of glucose, lipid, and energy metabolism through activation of the nuclear bile acid receptor farnesoid X receptor (FXR) and membrane G protein-coupled bile acid receptor-1 (Gpbar-1, aka TGR5). Agonist activation of FXR and TGR5 improves insulin and glucose sensitivity and stimulates energy metabolism to prevent diabetes, obesity, and non-alcoholic fatty liver disease (NAFLD). Bile acids have both pro- and anti-inflammatory actions through FXR and TGR5 in the intestine and liver. In the intestine, bile acids activate FXR and TGR5 to stimulate fibroblast growth factor 15 and glucagon-like peptide-1 secretion. FXR and TGR5 agonists may have therapeutic potential for treating liver-related metabolic diseases, such as diabetes and NAFLD. Keywords: Bile acid metabolism, Cholestatic liver diseases, Metabolic diseases
url http://www.sciencedirect.com/science/article/pii/S2542568417000071
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