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The Farnesoid X Receptor: Good for BAD

Diarrhea is a feature of several chronic intestinal disorders that are associated with increased delivery of bile acids into the colon. Although the prevalence of bile acid diarrhea is high, affecting approximately 1% of the adult population, current therapies often are unsatisfactory. By virtue of...

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Detalles Bibliográficos
Autores principales: Keely, Stephen J., Walters, Julian R.F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5247348/
https://www.ncbi.nlm.nih.gov/pubmed/28174746
http://dx.doi.org/10.1016/j.jcmgh.2016.08.004
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author Keely, Stephen J.
Walters, Julian R.F.
author_facet Keely, Stephen J.
Walters, Julian R.F.
author_sort Keely, Stephen J.
collection PubMed
description Diarrhea is a feature of several chronic intestinal disorders that are associated with increased delivery of bile acids into the colon. Although the prevalence of bile acid diarrhea is high, affecting approximately 1% of the adult population, current therapies often are unsatisfactory. By virtue of its capacity to inhibit colonic epithelial fluid secretion and to down-regulate hepatic bile acid synthesis through induction of the ileal fibroblast growth factor 19 release, the nuclear bile acid receptor, farnesoid X receptor, represents a promising target for the development of new therapeutic approaches. Here, we review our current understanding of the pathophysiology of bile acid diarrhea and the current evidence supporting a role for farnesoid X receptor agonists in treatment of the disease.
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spelling pubmed-52473482017-02-07 The Farnesoid X Receptor: Good for BAD Keely, Stephen J. Walters, Julian R.F. Cell Mol Gastroenterol Hepatol Review Diarrhea is a feature of several chronic intestinal disorders that are associated with increased delivery of bile acids into the colon. Although the prevalence of bile acid diarrhea is high, affecting approximately 1% of the adult population, current therapies often are unsatisfactory. By virtue of its capacity to inhibit colonic epithelial fluid secretion and to down-regulate hepatic bile acid synthesis through induction of the ileal fibroblast growth factor 19 release, the nuclear bile acid receptor, farnesoid X receptor, represents a promising target for the development of new therapeutic approaches. Here, we review our current understanding of the pathophysiology of bile acid diarrhea and the current evidence supporting a role for farnesoid X receptor agonists in treatment of the disease. Elsevier 2016-08-29 /pmc/articles/PMC5247348/ /pubmed/28174746 http://dx.doi.org/10.1016/j.jcmgh.2016.08.004 Text en © 2016 The Authors 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
Keely, Stephen J.
Walters, Julian R.F.
The Farnesoid X Receptor: Good for BAD
title The Farnesoid X Receptor: Good for BAD
title_full The Farnesoid X Receptor: Good for BAD
title_fullStr The Farnesoid X Receptor: Good for BAD
title_full_unstemmed The Farnesoid X Receptor: Good for BAD
title_short The Farnesoid X Receptor: Good for BAD
title_sort farnesoid x receptor: good for bad
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5247348/
https://www.ncbi.nlm.nih.gov/pubmed/28174746
http://dx.doi.org/10.1016/j.jcmgh.2016.08.004
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