Literature DB >> 25690590

FXR agonists as therapeutic agents for non-alcoholic fatty liver disease.

Rotonya M Carr1, Andrea E Reid.   

Abstract

Non-alcoholic fatty liver disease (NAFLD) is the hepatic manifestation of the metabolic syndrome and a risk factor for both cardiovascular and hepatic related morbidity and mortality. The increasing prevalence of this disease requires novel therapeutic approaches to prevent disease progression. Farnesoid X receptors are bile acid receptors with roles in lipid, glucose, and energy homeostasis. Synthetic farnesoid X receptor (FXR) agonists have been developed to specifically target these receptors for therapeutic use in NAFLD patients. Here, we present a review of bile acid physiology and how agonism of FXR receptors has been examined in pre-clinical and clinical NAFLD. Early evidence suggests a potential role for synthetic FXR agonists in the management of NAFLD; however, additional studies are needed to clarify their effects on lipid and glucose parameters in humans.

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Year:  2015        PMID: 25690590     DOI: 10.1007/s11883-015-0500-2

Source DB:  PubMed          Journal:  Curr Atheroscler Rep        ISSN: 1523-3804            Impact factor:   5.113


  105 in total

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3.  The TGR5 receptor mediates bile acid-induced itch and analgesia.

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Review 5.  Regulation of bile acid metabolism-related signaling pathways by gut microbiota in diseases.

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9.  FXR-Dependent Modulation of the Human Small Intestinal Microbiome by the Bile Acid Derivative Obeticholic Acid.

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Journal:  Gastroenterology       Date:  2018-08-23       Impact factor: 22.682

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