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Atherosclerosis and Lipoproteins |
From Royal Adelaide Hospital (P.K.), Adelaide, Australia; The Heart Research Institute (D.C., K.-A.R., P.J.B.), Sydney, Australia; University of Sydney (K.-A.R., P.J.B.), Australia; University of Melbourne (K.-A.R.), Australia; University of Western Australia (P.H.R.B.), Australia; Pfizer Global Research and Development (L.A.M.), Groton, Conn.
Correspondence to Philip Barter, The Heart Research Institute, 145 Missenden Road, Camperdown, New South Wales, Australia 2050. E-mail barterp{at}hri.org.au
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 on the kinetics of HDL CE transport in plasma.
Methods and Results Administration of a CETP inhibitor reduced CETP activity by 80% to 90% and doubled the HDL cholesteryl ester concentration. Multi-compartmental analysis was used to determine HDL CE kinetics in CETP-inhibited and control rabbits after injection of tracer amounts of both native and reconstituted HDL labeled with 3H in the CE moiety. In control rabbits, HDL CE was removed from plasma by both a direct pathway and an indirect pathway after transfer of HDL CE to the very-low-density lipoprotein/low-density lipoprotein fraction. In CETP-inhibited rabbits there was an almost complete block in removal via the indirect pathway. This did not compromise the overall removal of HDL CE from plasma, which was not different in control and inhibited animals.
Conclusion Inhibiting CETP in rabbits does not compromise the removal of HDL CE from plasma.
An 80% to 90% inhibition of plasma CETP activity in rabbits doubled the concentration of HDL CE by blocking its transfer to the VLDL/LDL fraction. However, this did not compromise the removal of HDL CE from plasma.
Key Words: cholesteryl esters high-density lipoprotein inhibitor kinetics reverse cholesterol transport
Related Article:
Arterioscler. Thromb. Vasc. Biol. 2006 26: 681-684.
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