Plasma Kinetics of Cholesteryl Ester Transfer Protein in the Rabbit
- 1 January 1997
- journal article
- Published by Wolters Kluwer Health in Arteriosclerosis, Thrombosis, and Vascular Biology
- Vol. 17 (1) , 203-210
- https://doi.org/10.1161/01.atv.17.1.203
Abstract
The plasma kinetics of recombinant human cholesteryl ester transfer protein (rCETP) were studied in six rabbits before and after cholesterol feeding (0.5% wt/wt). The rCETP, labeled with the use of the Bolton Hunter reagent, was shown to retain neutral lipid transfer activity. After intravenous infusion, labeled rCETP associated with rabbit lipoproteins to an extent similar to endogenous rabbit CETP (62% to 64% HDL associated). The plasma kinetics of CETP, modeled with the use of SAAM-II, conformed to a two-pool model, likely representing free and loosely HDL-associated CETP (fast pool) and a tightly apo (apolipoprotein) AI–associated (slow pool) CETP. The plasma residency time (chow diet) of the fast pool averaged 7.1 hours and of the slow pool, 76.3 hours. The production rate (PR) into and the fractional catabolic rate (FCR) of the fast pool were 20 and 10 times the PR and FCR, respectively, of the slow pool. In response to cholesterol feeding, CETP PR, FCR, and plasma mass increased by 416%, 60%, and 230%, respectively. There was a strong correlation ( r =.95, P =.003) between the increase in rabbit plasma CETP and the modeled increase in CETP PR in response to cholesterol feeding, suggesting that labeled human rCETP is a satisfactory tracer for rabbit plasma CETP. CETP is catabolized by distinct pools, likely corresponding to an apo AI–associated (slow) pool and a free and/or loosely HDL-associated (fast) pool. Factors that alter the affinity of CETP for HDL would be predicted to result in altered CETP catabolism. The effect of dietary cholesterol on plasma CETP mass can be explained largely by the effects on CETP synthesis, consistent with the observed effects of cholesterol on tissue mRNA levels.Keywords
This publication has 21 references indexed in Scilit:
- Kinetics and Inhibition of Lipid Exchange Catalyzed by Plasma Cholesteryl Ester Transfer Protein (Lipid transfer protein)Biochemistry, 1995
- Decreased cholesteryl ester transfer protein (CETP) mRNA and protein and increased high density lipoprotein following lipopolysaccharide administration in human CETP transgenic mice.Journal of Clinical Investigation, 1995
- Human ApoA-II inhibits the hydrolysis of HDL triglyceride and the decrease of HDL size induced by hypertriglyceridemia and cholesteryl ester transfer protein in transgenic mice.Journal of Clinical Investigation, 1994
- Selective Transfer of Cholesteryl Ester over Triglyceride by Human Plasma Lipid Transfer Protein between Apolipoprotein-Activated Lipid MicroemulsionsBiochemistry, 1994
- Dietary cholesterol increases transcription of the human cholesteryl ester transfer protein gene in transgenic mice. Dependence on natural flanking sequences.Journal of Clinical Investigation, 1992
- Mouse Apolipoprotein AI. cDNA-Derived Primary Structure, Gene Organisation and Complete Nucleotide SequenceBiological Chemistry Hoppe-Seyler, 1992
- The regulation of hepatic lipase and cholesteryl ester transfer protein activity in the cholesterol fed rabbitBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1991
- Plasma lipid transfer protein as a determinant of the atherogenicity of monkey plasma lipoproteins.Journal of Clinical Investigation, 1991
- Evaluation of pathways for the cellular uptake of high density lipoprotein cholesterol esters in rabbits.Journal of Clinical Investigation, 1991
- The primary structure of apolipoprotein A‐I from rabbit high‐density lipoproteinEuropean Journal of Biochemistry, 1986