Inhibitors of acyl-coenzyme a: cholesterol acyltransferase

Curr Drug Targets Cardiovasc Haematol Disord. 2005 Dec;5(6):463-9. doi: 10.2174/156800605774962040.

Abstract

Acyl-coenzyme A: cholesterol acyltransferase (ACAT) is an intracellular enzyme that catalyzes the formation of cholesterol esters from cholesterol and fatty acyl-coenzyme A. Animal experiments showed that ACAT inhibitors reduce plasma cholesterol levels by suppressing absorption of dietary cholesterol and by suppressing the assembly and secretion of apolipoprotein B-containing lipoproteins such as very low density lipoprotein in liver and chylomicron in intestine. Moreover, ACAT inhibitors were shown to prevent formation of macrophage-derived foam cells in the arterial walls. However, a recent double-blind, placebo-controlled, randomized trial of a potent ACAT inhibitor, avasimibe, failed to show significant beneficial effects on coronary atherosclerosis assessed by intravascular ultrasound. For clinical application of ACAT inhibitors, development of more potent compounds and improvements of the methods to evaluate their clinical efficacy are strongly needed.

Publication types

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

MeSH terms

  • Acetamides
  • Acetates / pharmacology
  • Acetates / therapeutic use
  • Animals
  • Cholesterol / blood
  • Double-Blind Method
  • Enzyme Inhibitors / pharmacology*
  • Enzyme Inhibitors / therapeutic use
  • Humans
  • Randomized Controlled Trials as Topic
  • Sterol O-Acyltransferase / antagonists & inhibitors*
  • Sterol O-Acyltransferase / metabolism
  • Sulfonamides
  • Sulfonic Acids / pharmacology
  • Sulfonic Acids / therapeutic use
  • Treatment Failure

Substances

  • Acetamides
  • Acetates
  • Enzyme Inhibitors
  • Sulfonamides
  • Sulfonic Acids
  • avasimibe
  • Cholesterol
  • Sterol O-Acyltransferase