Effects of CETP inhibition on triglyceride-rich lipoprotein composition and apoB-48 metabolism

被引:12
作者
Diffenderfer, Margaret R. [1 ]
Brousseau, Margaret E. [1 ]
Millar, John S. [3 ]
Barrett, P. Hugh R. [5 ,6 ,7 ]
Nartsupha, Chorthip [1 ]
Schaefer, Peter M. [1 ]
Wolfe, Megan L. [4 ]
Dolnikowski, Gregory G. [2 ]
Rader, Daniel J. [4 ]
Schaefer, Ernst J. [1 ]
机构
[1] Tufts Univ, Jean Mayer USDA Human Nutr Res Ctr Aging, Lipid Metab Lab, Boston, MA 02111 USA
[2] Tufts Univ, Jean Mayer USDA Human Nutr Res Ctr Aging, Mass Spectrometry Lab, Boston, MA 02111 USA
[3] Univ Penn, Sch Med, Inst Translat Med & Therapeut, Dept Pharmacol, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Inst Translat Med & Therapeut, Dept Med, Philadelphia, PA 19104 USA
[5] Univ Western Australia, Sch Med, Perth, WA 6009, Australia
[6] Univ Western Australia, Sch Pharmacol, Perth, WA 6009, Australia
[7] Univ Western Australia, Fac Engn Comp & Math, Perth, WA 6009, Australia
基金
美国国家卫生研究院;
关键词
cholesteryl ester transfer protein; apolipoprotein; lipoprotein kinetics; postprandial metabolism; torcetrapib; ESTER TRANSFER PROTEIN; APO-A-I; B-CONTAINING LIPOPROTEINS; CORONARY-ARTERY-DISEASE; IIB HYPERLIPIDEMIA; APOLIPOPROTEIN-B; LOW-DENSITY; POSTPRANDIAL STATE; HDL-CHOLESTEROL; BLOOD-PRESSURE;
D O I
10.1194/jlr.M019570
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cholesteryl ester transfer protein (CETP) facilitates the transfer of HDL cholesteryl ester to triglyceride-rich lipoproteins (TRL). This study aimed to determine the effects of CETP inhibition with torcetrapib on TRL composition and apoB-48 metabolism. Study subjects with low HDL cholesterol (<40 mg/dl), either untreated (n = 9) or receiving atorvastatin 20 mg daily (n = 9), received placebo for 4 weeks, followed by torcetrapib 120 mg once daily for the next 4 weeks. A subset of the subjects not treated with atorvastatin participated in a third phase (n = 6), in which they received torcetrapib 120 mg twice daily for an additional 4 weeks. At the end of each phase, all subjects received a primed-constant infusion of [5,5,5-H-2(3)] L-leucine, while in the constantly fed state, to determine the kinetics of TRL apoB-48 and TRL composition. Relative to placebo, torcetrapib markedly reduced TRL CE levels in all groups (>=-69%; P < 0.005). ApoB-48 pool size (PS) and production rate (PR) decreased in the nonatorvastatin once daily (PS: -49%, P = 0.007; PR: -49%, P = 0.005) and twice daily (PS: -30%, P = 0.01; PR: -27%, P = 0.13) cohorts. In the atorvastatin cohort, apoB-48 PS and PR, which were already lowered by atorvastatin, did not change with torcetrapib. Our findings indicate that CETP inhibition reduced plasma apoB-48 concentrations by reducing apoB-48 production but did not have this effect in subjects already treated with atorvastatin.-Diffenderfer, M. R., M. E. Brousseau, J. S. Millar, P. H. R. Barrett, C. Nartsupha, P. M. Schaefer, M. L. Wolfe, G. G. Dolnikowski, D. J. Rader, and E. J. Schaefer. Effects of CETP inhibition on triglyceride-rich lipoprotein composition and apoB-48 metabolism. J. Lipid Res. 2012. 53: 1190-1199.
引用
收藏
页码:1190 / 1199
页数:10
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