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Bile acid nuclear receptor FXR and digestive system diseases

Bile acids (BAs) are not only digestive surfactants but also important cell signaling molecules, which stimulate several signaling pathways to regulate some important biological processes. The bile-acid-activated nuclear receptor, farnesoid X receptor (FXR), plays a pivotal role in regulating bile a...

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Detalles Bibliográficos
Autores principales: Ding, Lili, Yang, Li, Wang, Zhengtao, Huang, Wendong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629217/
https://www.ncbi.nlm.nih.gov/pubmed/26579439
http://dx.doi.org/10.1016/j.apsb.2015.01.004
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author Ding, Lili
Yang, Li
Wang, Zhengtao
Huang, Wendong
author_facet Ding, Lili
Yang, Li
Wang, Zhengtao
Huang, Wendong
author_sort Ding, Lili
collection PubMed
description Bile acids (BAs) are not only digestive surfactants but also important cell signaling molecules, which stimulate several signaling pathways to regulate some important biological processes. The bile-acid-activated nuclear receptor, farnesoid X receptor (FXR), plays a pivotal role in regulating bile acid, lipid and glucose homeostasis as well as in regulating the inflammatory responses, barrier function and prevention of bacterial translocation in the intestinal tract. As expected, FXR is involved in the pathophysiology of a wide range of diseases of gastrointestinal tract, including inflammatory bowel disease, colorectal cancer and type 2 diabetes. In this review, we discuss current knowledge of the roles of FXR in physiology of the digestive system and the related diseases. Better understanding of the roles of FXR in digestive system will accelerate the development of FXR ligands/modulators for the treatment of digestive system diseases.
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spelling pubmed-46292172015-11-17 Bile acid nuclear receptor FXR and digestive system diseases Ding, Lili Yang, Li Wang, Zhengtao Huang, Wendong Acta Pharm Sin B Review Bile acids (BAs) are not only digestive surfactants but also important cell signaling molecules, which stimulate several signaling pathways to regulate some important biological processes. The bile-acid-activated nuclear receptor, farnesoid X receptor (FXR), plays a pivotal role in regulating bile acid, lipid and glucose homeostasis as well as in regulating the inflammatory responses, barrier function and prevention of bacterial translocation in the intestinal tract. As expected, FXR is involved in the pathophysiology of a wide range of diseases of gastrointestinal tract, including inflammatory bowel disease, colorectal cancer and type 2 diabetes. In this review, we discuss current knowledge of the roles of FXR in physiology of the digestive system and the related diseases. Better understanding of the roles of FXR in digestive system will accelerate the development of FXR ligands/modulators for the treatment of digestive system diseases. Elsevier 2015-03 2015-02-25 /pmc/articles/PMC4629217/ /pubmed/26579439 http://dx.doi.org/10.1016/j.apsb.2015.01.004 Text en © 2015 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Ding, Lili
Yang, Li
Wang, Zhengtao
Huang, Wendong
Bile acid nuclear receptor FXR and digestive system diseases
title Bile acid nuclear receptor FXR and digestive system diseases
title_full Bile acid nuclear receptor FXR and digestive system diseases
title_fullStr Bile acid nuclear receptor FXR and digestive system diseases
title_full_unstemmed Bile acid nuclear receptor FXR and digestive system diseases
title_short Bile acid nuclear receptor FXR and digestive system diseases
title_sort bile acid nuclear receptor fxr and digestive system diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629217/
https://www.ncbi.nlm.nih.gov/pubmed/26579439
http://dx.doi.org/10.1016/j.apsb.2015.01.004
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