Interaction of rabbit lipoproteins and red blood cells with liposomes of egg yolk phospholipids |
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Authors: | Armando J. Mendez Jin Lin He Hui Sheng Huang Shu Rong Wen S. L. Hsia |
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Affiliation: | (1) Lipid Profile Evaluation Laboratory, Department of Dermatology and Cutaneous Surgery, University of Miami School of Medicine, 33101 FL, Miami;(2) Department of Biochemistry and Molecular Biology, University of Miami School of Medicine, 33101 Miami, FL;(3) Present address: Division of Metabolism, Endocrinology and Nutrition, RG-26, University of Washington, 98195 Seattle, WA;(4) University of Miami School of Medicine, P.O. Box 016960, R-117, 33101 Miami, FL |
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Abstract: | After intravenous injection of liposomes prepared from egg yolk phospholipids into rabbits, the phospholipids were readily assimilated by the lipoproteins, and there were increases in the circulating levels of cholesterol and phospholipids. The increases in cholesterol level were mainly due to increases of free cholesterol. Gradient ultracentrifugation showed that the lipoproteins decreased in density, and gel filtration chromatography showed that they increased in particle size. Upon electrophoresis, they exhibited slower mobility. Liposomes recovered from rabbits 3 hr after the injection contained free cholesterol, apolipoproteins A-I, E and traces of C. The apolipoprotein may target the liposomes for uptake by hepatocytes. Incubation of the liposomes with rabbit red blood cell membranes in vitro caused a decrease in cholesterol content of the membranes. However, the cholesterol/phosphate ratio in red blood cells isolated from the rabbits after the injection of liposomes did not change significantly, suggesting rapid replenishment of red blood cell cholesterol in vivo, possibly by equilibration with lipoprotein cholesterol or tissue cholesterol. These results suggest that the injection of phospholipid liposomes may have an antiatherogenic effect by the removal of tissue cholesterol and enhancing hepatic disposal of cholesterol through the reverse cholesterol transport mechanism. |
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