Abstract
Cholestatic liver diseases encompass a wide spectrum of disorders with different causes, resulting in impaired bile flow and accumulation of bile acids and other potentially hepatotoxic cholephils. The understanding of the molecular mechanisms of bile formation and cholestasis has recently improved significantly through new insights into nuclear receptor (patho)biology. Nuclear receptors are ligand-activated transcription factors, which act as central players in the regulation of genes responsible for elimination and detoxification of biliary constituents accumulating in cholestasis. They also control other pathophysiologic processes such as inflammation, fibrogenesis, and carcinogenesis involved in the pathogenesis and disease progression of cholestasis liver diseases.
Copyright © 2013 Elsevier Inc. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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Bile Acids and Salts / biosynthesis*
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Cholagogues and Choleretics / therapeutic use
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Cholestasis / drug therapy*
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Cholestasis / genetics
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Cholestasis / metabolism*
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Constitutive Androstane Receptor
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Homeostasis / drug effects
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Humans
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Ligands
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Peroxisome Proliferator-Activated Receptors / metabolism
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Pregnane X Receptor
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Receptors, Calcitriol / genetics
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Receptors, Calcitriol / metabolism
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Receptors, Cytoplasmic and Nuclear / agonists
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Receptors, Cytoplasmic and Nuclear / genetics
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Receptors, Cytoplasmic and Nuclear / metabolism*
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Receptors, Glucocorticoid / metabolism
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Receptors, Steroid / genetics
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Receptors, Steroid / metabolism
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Signal Transduction / drug effects*
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Signal Transduction / genetics
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Ursodeoxycholic Acid / therapeutic use
Substances
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Bile Acids and Salts
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Cholagogues and Choleretics
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Constitutive Androstane Receptor
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Ligands
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Peroxisome Proliferator-Activated Receptors
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Pregnane X Receptor
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Receptors, Calcitriol
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Receptors, Cytoplasmic and Nuclear
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Receptors, Glucocorticoid
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Receptors, Steroid
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farnesoid X-activated receptor
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Ursodeoxycholic Acid