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Recent advances in understanding bile acid homeostasis
Bile acids are derived from cholesterol to facilitate intestinal nutrient absorption and biliary secretion of cholesterol. Recent studies have identified bile acids as signaling molecules that activate nuclear farnesoid X receptor (FXR) and membrane G protein-coupled bile acid receptor-1 (Gpbar-1, a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000 Research Limited
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698910/ https://www.ncbi.nlm.nih.gov/pubmed/29188025 http://dx.doi.org/10.12688/f1000research.12449.1 |
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author | Chiang, John YL |
author_facet | Chiang, John YL |
author_sort | Chiang, John YL |
collection | PubMed |
description | Bile acids are derived from cholesterol to facilitate intestinal nutrient absorption and biliary secretion of cholesterol. Recent studies have identified bile acids as signaling molecules that activate nuclear farnesoid X receptor (FXR) and membrane G protein-coupled bile acid receptor-1 (Gpbar-1, also known as TGR5) to maintain metabolic homeostasis and protect liver and other tissues and cells from bile acid toxicity. Bile acid homeostasis is regulated by a complex mechanism of feedback and feedforward regulation that is not completely understood. This review will cover recent advances in bile acid signaling and emerging concepts about the classic and alternative bile acid synthesis pathway, bile acid composition and bile acid pool size, and intestinal bile acid signaling and gut microbiome in regulation of bile acid homeostasis. |
format | Online Article Text |
id | pubmed-5698910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-56989102017-11-28 Recent advances in understanding bile acid homeostasis Chiang, John YL F1000Res Review Bile acids are derived from cholesterol to facilitate intestinal nutrient absorption and biliary secretion of cholesterol. Recent studies have identified bile acids as signaling molecules that activate nuclear farnesoid X receptor (FXR) and membrane G protein-coupled bile acid receptor-1 (Gpbar-1, also known as TGR5) to maintain metabolic homeostasis and protect liver and other tissues and cells from bile acid toxicity. Bile acid homeostasis is regulated by a complex mechanism of feedback and feedforward regulation that is not completely understood. This review will cover recent advances in bile acid signaling and emerging concepts about the classic and alternative bile acid synthesis pathway, bile acid composition and bile acid pool size, and intestinal bile acid signaling and gut microbiome in regulation of bile acid homeostasis. F1000 Research Limited 2017-11-20 /pmc/articles/PMC5698910/ /pubmed/29188025 http://dx.doi.org/10.12688/f1000research.12449.1 Text en Copyright: © 2017 Chiang JY http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Chiang, John YL Recent advances in understanding bile acid homeostasis |
title | Recent advances in understanding bile acid homeostasis |
title_full | Recent advances in understanding bile acid homeostasis |
title_fullStr | Recent advances in understanding bile acid homeostasis |
title_full_unstemmed | Recent advances in understanding bile acid homeostasis |
title_short | Recent advances in understanding bile acid homeostasis |
title_sort | recent advances in understanding bile acid homeostasis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698910/ https://www.ncbi.nlm.nih.gov/pubmed/29188025 http://dx.doi.org/10.12688/f1000research.12449.1 |
work_keys_str_mv | AT chiangjohnyl recentadvancesinunderstandingbileacidhomeostasis |