Cholesteryl ester transfer protein inhibition: effect on reverse cholesterol transport?

نویسندگان

  • Patrick C N Rensen
  • Louis M Havekes
چکیده

Statins, inhibitors of the key enzyme in the biosynthesis of cholesterol (ie, 3-hydroxy-3-methylglutaryl [HMG]coenzyme A [CoA] reductase), are widely used as the prevailing strategy to combat atherosclerosis through reducing LDL cholesterol levels. Large-scale clinical trials have shown that statins markedly reduce coronary events.1,2 A meta-analysis of 22 studies enrolling nearly 70 000 individuals indicated that an effective decrease of LDL cholesterol by 20% to 40% reduces non-fatal myocardial infarction or coronary heart disease mortality by 25%.3 Although of clear clinical benefit, lowering LDL cholesterol alone using statin monotherapy thus does not prevent 75% of all cardiovascular events, which has led to a considerable interest in targeting other lipid-related risk factors.

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The effect of cholesteryl ester transfer protein overexpression and inhibition on reverse cholesterol transport.

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OBJECTIVE Inhibitors of cholesteryl ester transfer protein (CETP) have been developed as potential anti-atherogenic agents. Theoretically, however, they may be pro-atherogenic by blocking one of the pathways for removing high-density lipoprotein (HDL) cholesteryl esters (CE) from plasma in the final step of reverse cholesterol transport. Here we describe how CETP inhibition in rabbits impacts o...

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Plasma lipid transfer proteins.

The plasma lipid transfer proteins mediate the transfer and exchange of phospholipids and neutral lipids between the plasma lipoproteins. The cholesteryl ester transfer protein (CETP) and the phospholipid transfer protein (PLTP) are members of the lipid transfer/lipopolysaccharide binding gene family. The CETP contains binding sites for cholesteryl ester and triglycerides and probably acts by a...

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عنوان ژورنال:
  • Arteriosclerosis, thrombosis, and vascular biology

دوره 26 4  شماره 

صفحات  -

تاریخ انتشار 2006