Transcriptional Regulation of Metabolic Pathways via Lipid-Sensing Nuclear Receptors PPARs, FXR, and LXR in NASH

Cell Mol Gastroenterol Hepatol. 2021;11(5):1519-1539. doi: 10.1016/j.jcmgh.2021.01.012. Epub 2021 Feb 2.

Abstract

Nonalcoholic fatty liver disease comprises a wide spectrum of liver injuries from simple steatosis to steatohepatitis and cirrhosis. Nonalcoholic steatohepatitis (NASH) is defined when liver steatosis is associated with inflammation, hepatocyte damage, and fibrosis. A genetic predisposition and environmental insults (ie, dietary habits, obesity) are putatively responsible for NASH progression. Here, we present the impact of the lipid-sensing nuclear receptors in the pathogenesis and treatment of NASH. In detail, we discuss the pros and cons of the putative transcriptional action of the fatty acid sensors (peroxisome proliferator-activated receptors), the bile acid sensor (farnesoid X receptor), and the oxysterol sensor (liver X receptors) in the pathogenesis and bona fide treatment of NASH.

Keywords: Farnesoid X Receptor (FXR); Liver X Receptor (LXR); Nonalcoholic Steatohepatitis (NASH); Nuclear Receptors; Peroxisome Proliferator Activated Receptors (PPARs).

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Gene Expression Regulation*
  • Humans
  • Lipids / analysis*
  • Liver X Receptors / metabolism*
  • Metabolic Networks and Pathways*
  • Non-alcoholic Fatty Liver Disease / genetics
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Non-alcoholic Fatty Liver Disease / pathology*
  • Peroxisome Proliferator-Activated Receptors / metabolism*
  • Receptors, Cytoplasmic and Nuclear / metabolism*

Substances

  • Lipids
  • Liver X Receptors
  • Peroxisome Proliferator-Activated Receptors
  • Receptors, Cytoplasmic and Nuclear
  • farnesoid X-activated receptor