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Regulation of reverse cholesterol transport and clinical implications.

Abstract
Plasma levels of high-density lipoprotein (HDL) cholesterol and its major protein, apolipoprotein A-I, are inversely correlated with the incidence of atherosclerotic cardiovascular disease. Low HDL cholesterol and apolipoprotein A-I levels often are found in association with other cardiovascular risk factors, including the metabolic syndrome, insulin resistance, and type 2 diabetes mellitus. However, overexpression of apolipoprotein A-I in animals has been shown to reduce progression and even induce regression of atherosclerosis, indicating that apolipoprotein A-I is directly protective against atherosclerosis. A major mechanism by which apolipoprotein A-I inhibits atherosclerosis may be by promoting cholesterol efflux from macrophages and returning it to the liver for excretion, a process termed reverse cholesterol transport. This article focuses on new developments in the regulation of reverse cholesterol transport and the clinical implications of those developments.
AuthorsDaniel J Rader
JournalThe American journal of cardiology (Am J Cardiol) Vol. 92 Issue 4A Pg. 42J-49J (Aug 18 2003) ISSN: 0002-9149 [Print] United States
PMID12957326 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • ATP Binding Cassette Transporter 1
  • ATP-Binding Cassette Transporters
  • Apolipoprotein A-I
  • CD36 Antigens
  • CETP protein, human
  • Carrier Proteins
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL
  • Glycoproteins
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Hypolipidemic Agents
  • Membrane Proteins
  • Phospholipid Transfer Proteins
  • Receptors, Immunologic
  • Receptors, Lipoprotein
  • Receptors, Scavenger
  • Scarb1 protein, mouse
  • Scavenger Receptors, Class B
  • Niacin
  • LIPG protein, human
  • Lipase
  • Lipg protein, mouse
  • Lipoprotein Lipase
Topics
  • ATP Binding Cassette Transporter 1
  • ATP-Binding Cassette Transporters (genetics)
  • Animals
  • Apolipoprotein A-I (genetics)
  • Biological Transport (genetics, physiology)
  • CD36 Antigens (genetics)
  • Cardiovascular Diseases (prevention & control)
  • Carrier Proteins (genetics)
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL (genetics, metabolism)
  • Glycoproteins
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors (therapeutic use)
  • Hypolipidemic Agents (therapeutic use)
  • Hypolipoproteinemias (drug therapy, genetics, metabolism)
  • Lipase (genetics)
  • Lipoprotein Lipase (genetics)
  • Membrane Proteins (genetics)
  • Mice
  • Niacin (therapeutic use)
  • Phospholipid Transfer Proteins
  • Receptors, Immunologic
  • Receptors, Lipoprotein
  • Receptors, Scavenger
  • Risk Factors
  • Scavenger Receptors, Class B

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