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Therapeutic Roles of Bile Acid Signaling in Chronic Liver Diseases

Bile acids (BAs) are the major metabolic product of cholesterol, having detergent-like activities and being responsible for absorption of lipid and lipid-soluble vitamins. In addition, it has been increasingly recognized that BAs are important signaling molecules, regulating energy metabolism and im...

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Detalles Bibliográficos
Autores principales: Li, Yan, Lu, Lun-Gen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328738/
https://www.ncbi.nlm.nih.gov/pubmed/30637221
http://dx.doi.org/10.14218/JCTH.2018.00025
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author Li, Yan
Lu, Lun-Gen
author_facet Li, Yan
Lu, Lun-Gen
author_sort Li, Yan
collection PubMed
description Bile acids (BAs) are the major metabolic product of cholesterol, having detergent-like activities and being responsible for absorption of lipid and lipid-soluble vitamins. In addition, it has been increasingly recognized that BAs are important signaling molecules, regulating energy metabolism and immunity. Under physiological circumstances, synthesis and transport of BAs are precisely regulated to maintain bile acid homeostasis. Disruption of bile acid homeostasis results in pathological cholestasis and metabolic liver diseases. During the last decades, BAs have been gradually recognized as an important therapeutic target for novel treatment in chronic liver diseases. This review will provide an update on the current understanding of synthesis, transport and regulation of BAs, with a focus on the therapeutic roles of bile acid signaling in chronic liver diseases.
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spelling pubmed-63287382019-01-11 Therapeutic Roles of Bile Acid Signaling in Chronic Liver Diseases Li, Yan Lu, Lun-Gen J Clin Transl Hepatol Review Article Bile acids (BAs) are the major metabolic product of cholesterol, having detergent-like activities and being responsible for absorption of lipid and lipid-soluble vitamins. In addition, it has been increasingly recognized that BAs are important signaling molecules, regulating energy metabolism and immunity. Under physiological circumstances, synthesis and transport of BAs are precisely regulated to maintain bile acid homeostasis. Disruption of bile acid homeostasis results in pathological cholestasis and metabolic liver diseases. During the last decades, BAs have been gradually recognized as an important therapeutic target for novel treatment in chronic liver diseases. This review will provide an update on the current understanding of synthesis, transport and regulation of BAs, with a focus on the therapeutic roles of bile acid signaling in chronic liver diseases. XIA & HE Publishing Inc. 2018-10-25 2018-12-28 /pmc/articles/PMC6328738/ /pubmed/30637221 http://dx.doi.org/10.14218/JCTH.2018.00025 Text en © 2018 Authors. http://creativecommons.org/licenses/by-nc/4.0/ This article has been published under the terms of Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0), which permits noncommercial unrestricted use, distribution, and reproduction in any medium, provided that the following statement is provided. “This article has been published in Journal of Clinical and Translational Hepatology at DOI: 10.14218/JCTH.2018.00025 and can also be viewed on the Journal’s website at http://www.jcthnet.com”.
spellingShingle Review Article
Li, Yan
Lu, Lun-Gen
Therapeutic Roles of Bile Acid Signaling in Chronic Liver Diseases
title Therapeutic Roles of Bile Acid Signaling in Chronic Liver Diseases
title_full Therapeutic Roles of Bile Acid Signaling in Chronic Liver Diseases
title_fullStr Therapeutic Roles of Bile Acid Signaling in Chronic Liver Diseases
title_full_unstemmed Therapeutic Roles of Bile Acid Signaling in Chronic Liver Diseases
title_short Therapeutic Roles of Bile Acid Signaling in Chronic Liver Diseases
title_sort therapeutic roles of bile acid signaling in chronic liver diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328738/
https://www.ncbi.nlm.nih.gov/pubmed/30637221
http://dx.doi.org/10.14218/JCTH.2018.00025
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