Contribution of apoB-48 and apoB-100 triglyceride-rich lipoproteins (TRL) to postprandial increases in the plasma concentration of TRL triglycerides and retinyl esters.

JS Cohn, EJ Johnson, JS Millar, SD Cohn… - Journal of Lipid …, 1993 - Elsevier
JS Cohn, EJ Johnson, JS Millar, SD Cohn, RW Milne, YL Marcel, RM Russell, EJ Schaefer
Journal of Lipid Research, 1993Elsevier
After the ingestion of a fat-rich meal, there is a postprandial increase in the plasma
concentration of both apolipoprotein B-48-and apoB-100-containing triglyceride-rich
lipoproteins (apoB-48 and apoB-100 TRL). In order to determine the contribution of these
lipoproteins to postprandial lipemia, the concentration of triglycerides (TG) and retinyl esters
(RE) was measured in apoB-48 and apoB-100 TRL after an oral fat load. Six normolipidemic
male subjects were fed heavy cream (1 g fat per kg body weight) containing vitamin A (3000 …
After the ingestion of a fat-rich meal, there is a postprandial increase in the plasma concentration of both apolipoprotein B-48- and apoB-100-containing triglyceride-rich lipoproteins (apoB-48 and apoB-100 TRL). In order to determine the contribution of these lipoproteins to postprandial lipemia, the concentration of triglycerides (TG) and retinyl esters (RE) was measured in apoB-48 and apoB-100 TRL after an oral fat load. Six normolipidemic male subjects were fed heavy cream (1 g fat per kg body weight) containing vitamin A (3000 retinol equivalents). TRL were isolated by ultracentrifugation from plasma samples obtained at regular intervals after the meal, and apoB-100 TRL were separated from apoB-48 TRL by affinity chromatography using monoclonal antibodies. Postprandial increase in plasma TG concentration was due to an increase in TG in the TRL fraction, which in turn was predominantly (82 +/- 4%) due to an increase in TG in apoB-48 TRL. Contribution of apoB-100 TRL to postprandial increase in TRL TG was 3-27% in individual subjects. ApoB-100 TRL remained a significant carrier of total plasma triglyceride in the fed state, as reflected by similar apoB-100 and apoB-48 TRL TG concentrations at 2, 4, and 6 h after the fat meal. Retinyl esters were regularly detected in apoB-100 TRL. Seventy-five (+/- 9) percent of the increase in TRL-RE was due to RE in apoB-48 TRL and 25 +/- 9% was due to RE in apoB-100. These data suggest that RE in plasma are not always associated with apoB-48-containing lipoproteins. Furthermore, we conclude that apoB-100 TRL, as well as apoB-48 TRL, make a significant contribution to postprandial triglyceridemia.
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