Atherosclerosis: lessons from LXR and the intestine

Trends Endocrinol Metab. 2013 Mar;24(3):120-8. doi: 10.1016/j.tem.2012.10.004. Epub 2012 Nov 15.

Abstract

Modulation of the cholesterol-sensing liver X receptors (LXRs) and their downstream targets has emerged as promising therapeutic avenues in atherosclerosis. The intestine is important for its unique capabilities to act as a gatekeeper for cholesterol absorption and to participate in the process of cholesterol elimination in the feces and reverse cholesterol transport (RCT). Pharmacological and genetic intestine-specific LXR activation have been shown to protect against atherosclerosis. In this review we discuss the LXR-targeted molecular players in the enterocytes as well as the intestine-driven pathways contributing to cholesterol homeostasis with therapeutic potential as targets in the prevention and treatment of atherosclerosis..

Publication types

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

MeSH terms

  • ATP Binding Cassette Transporter 1 / physiology
  • ATP Binding Cassette Transporter, Subfamily G, Member 5
  • ATP Binding Cassette Transporter, Subfamily G, Member 8
  • ATP-Binding Cassette Transporters / genetics
  • Animals
  • Atherosclerosis / drug therapy*
  • Atherosclerosis / prevention & control
  • Cholesterol / metabolism*
  • Homeostasis
  • Humans
  • Hypercholesterolemia / drug therapy
  • Intestinal Absorption / physiology
  • Intestinal Mucosa / metabolism*
  • Lipoproteins / genetics
  • Liver X Receptors
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology
  • Membrane Transport Proteins
  • Orphan Nuclear Receptors / physiology*
  • Sterol O-Acyltransferase / physiology
  • Sterol O-Acyltransferase 2

Substances

  • ABCG5 protein, human
  • ABCG8 protein, human
  • ATP Binding Cassette Transporter 1
  • ATP Binding Cassette Transporter, Subfamily G, Member 5
  • ATP Binding Cassette Transporter, Subfamily G, Member 8
  • ATP-Binding Cassette Transporters
  • Lipoproteins
  • Liver X Receptors
  • Membrane Proteins
  • Membrane Transport Proteins
  • NPC1L1 protein, human
  • Orphan Nuclear Receptors
  • Cholesterol
  • Sterol O-Acyltransferase