Nuclear receptors and nonalcoholic fatty liver diseases

被引:269
作者
Cave, Matthew C. [1 ,2 ,3 ,4 ,5 ]
Clair, Heather B. [2 ]
Hardesty, Josiah E. [2 ]
Falkner, K. Cameron [1 ]
Feng, Wenke [1 ,3 ]
Clark, Barbara J. [2 ]
Sidey, Jennifer [2 ]
Shi, Hongxue [3 ]
Aqel, Bashar A. [6 ]
McClain, Craig J. [1 ,3 ,4 ,5 ]
Prough, Russell A. [2 ]
机构
[1] Univ Louisville, Div Gastroenterol Hepatol & Nutr, Dept Med, Sch Med, Louisville, KY 40202 USA
[2] Univ Louisville, Dept Biochem & Mol Genet, Sch Med, Louisville, KY 40202 USA
[3] Univ Louisville, Dept Pharmacol & Toxicol, Sch Med, Louisville, KY 40202 USA
[4] Robley Rex Vet Affairs Med Ctr, Louisville, KY 40206 USA
[5] KentuckyOne Hlth Jewish Hosp, Liver Transplant Program, Louisville, KY 40202 USA
[6] Mayo Clin, Dept Med, Coll Med, Div Gastroenterol & Hepatol, Scottsdale, AZ 85054 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2016年 / 1859卷 / 09期
关键词
NAFLD; NASH; TAFLD; TASH; PCBs; PXR; LXR; FXR; CAR; PPAR; CONSTITUTIVE ANDROSTANE RECEPTOR; PREGNANE-X-RECEPTOR; FIBROBLAST-GROWTH-FACTOR; NF-KAPPA-B; PROLIFERATOR-ACTIVATED RECEPTORS; PEROXISOMAL BETA-OXIDATION; RESPONSIVE ENHANCER MODULE; LXR INVERSE AGONIST; GENE-EXPRESSION; BILE-ACIDS;
D O I
10.1016/j.bbagrm.2016.03.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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 proliferatoractivated 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. Nonalcoholic 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. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:1083 / 1099
页数:17
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