Article ID Journal Published Year Pages File Type
1967909 Clinica Chimica Acta 2007 7 Pages PDF
Abstract

BackgroundCholesteryl ester transfer protein (CETP) is suggested to be involved in the cholesterol level in remnant like lipoprotein particles (RLP), but there is no direct evidence that CETP increases cholesterol-rich RLP in plasma.MethodsHuman plasma was incubated with or without HDL containing [3H]-labeled cholesteryl ester ([3H]CE), recombinant CETP or CETP inhibitors at 37 °C in vitro.ResultsThe RLP–cholesterol (RLP–C) level increased time-dependently and the amount of RLP–C increase (ΔRLP–C) by the incubation was positively correlated with triglyceride (TG) level in plasma (r = 0.597, P = 0.0070). [3H]CE in HDL was transferred to RLP fraction under 37 °C incubation, and the amount of [3H]CE transferred to RLP correlated significantly with ΔRLP–C in plasma (r = 0.611, P = 0.0156). Human recombinant CETP enhanced the RLP–C increase, while CETP inhibitor JTT-705 and anti-human CETP monoclonal antibody inhibited both the RLP–C increase and [3H]CE transfer to RLP. On the other hand, an inhibition of lecithin: cholesterol acyltransferase (LCAT) did not affect the RLP–C increase. In triglyceride-rich lipoproteins (TRL) fraction, JTT-705 inhibited [3H]CE transfer to RLP more strongly than that to non-RLP.ConclusionsCETP promotes the formation of cholesterol-rich RLP through the transfer of CE from HDL to TRL and CETP inhibitors are useful to reduce RLP–C.

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