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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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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. |
format | Online Article Text |
id | pubmed-5247348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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