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Nuclear receptors and nonalcoholic fatty liver disease
- Source :
- Biochimica et biophysica acta. 1859(9)
- Publication Year :
- 2015
-
Abstract
- Nuclear receptors are transcription factors which sense changing environmental or hormonal signals and effect transcriptional changes to regulate core life functions including growth, development, and reproduction. To support this function, following ligand-activation by xenobiotics, members of subfamily 1 nuclear receptors (NR1s) may heterodimerize with the retinoid X receptor (RXR) to regulate transcription of genes involved in energy and xenobiotic metabolism and inflammation. Several of these receptors including the peroxisome proliferator-activated receptors (PPARs), the pregnane and xenobiotic receptor (PXR), the constitutive androstane receptor (CAR), the liver X receptor (LXR) and the farnesoid X receptor (FXR) are key regulators of the gut:liver:adipose axis and serve to coordinate metabolic responses across organ systems between the fed and fasting states. Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease and may progress to cirrhosis and even hepatocellular carcinoma. NAFLD is associated with inappropriate nuclear receptor function and perturbations along the gut:liver:adipose axis including obesity, increased intestinal permeability with systemic inflammation, abnormal hepatic lipid metabolism, and insulin resistance. Environmental chemicals may compound the problem by directly interacting with nuclear receptors leading to metabolic confusion and the inability to differentiate fed from fasting conditions. This review focuses on the impact of nuclear receptors in the pathogenesis and treatment of NAFLD. Clinical trials including PIVENS and FLINT demonstrate that nuclear receptor targeted therapies may lead to the paradoxical dissociation of steatosis, inflammation, fibrosis, insulin resistance, dyslipidemia and obesity. Novel strategies currently under development (including tissue-specific ligands and dual receptor agonists) may be required to separate the beneficial effects of nuclear receptor activation from unwanted metabolic side effects. The impact of nuclear receptor crosstalk in NAFLD is likely to be profound, but requires further elucidation. This article is part of a Special Issue entitled: Xenobiotic nuclear receptors: New Tricks for An Old Dog, edited by Dr. Wen Xie.
- Subjects :
- 0301 basic medicine
medicine.medical_specialty
Receptors, Steroid
Peroxisome Proliferator-Activated Receptors
Biophysics
Receptors, Cytoplasmic and Nuclear
Biology
Retinoid X receptor
Biochemistry
Article
Xenobiotics
03 medical and health sciences
Structural Biology
Non-alcoholic Fatty Liver Disease
Internal medicine
Constitutive androstane receptor
Genetics
medicine
Animals
Humans
Liver X receptor
Molecular Biology
Constitutive Androstane Receptor
Liver X Receptors
Pregnane X receptor
Liver receptor homolog-1
Pregnane X Receptor
Drugs, Investigational
Receptor Cross-Talk
030104 developmental biology
Endocrinology
Nuclear receptor
Adipose Tissue
Gene Expression Regulation
Liver
Farnesoid X receptor
Peroxisome proliferator-activated receptor alpha
Energy Metabolism
Signal Transduction
Subjects
Details
- ISSN :
- 00063002
- Volume :
- 1859
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- Biochimica et biophysica acta
- Accession number :
- edsair.doi.dedup.....a7766eb122a434348b75f559704eba35