Abstract

Very low density lipoprotein (VLDL) and low density lipoprotein (LDL) apoprotein (apo)-B turnover rates were measured simultaneously by injecting 131I-labeled VLDL and 125I-labeled LDL into fasting baboons (Papio sp.) selectively bred for high serum cholesterol levels and having either low or high LDL levels. The radioactivities in VLDL, intermediate density lipoprotein (IDL), LDL apoB, and urine were measured at intervals between 5 min and 6 days. Kinetic parameters for apoB were calculated in each baboon fed a chow diet or a high cholesterol, high fat diet (HCHF). VLDL apoB residence times were similar in the two groups of animals fed chow; they were increased by HCHF feeding in high LDL animals, but not in low LDL animals. Production rates of VLDL apoB were decreased by the HCHF diet in both high and low LDL animals. Most of the radioactivity from VLDL apoB was transferred to IDL. However, a greater proportion of radioactivity was removed directly from IDL apoB in low LDL animals than in high LDL animals, and only about one-third appeared in LDL. In high LDL animals, a greater proportion of this radioactivity was converted to LDL (61.4 +/- 7.2% in chow-fed animals and 49.2 +/- 10.9% in animals fed the HCHF diet; mean +/- SEM, n = 5). Production rates for LDL apoB were higher in high LDL animals than those in low LDL animals on both diets. The HCHF diet increased residence times of LDL apoB without changing production rates in both groups. VLDL apoB production was not sufficient to account for LDL apoB production in high LDL animals, a finding that suggested that a large amount of LDL apoB was derived from a source other than VLDL apoB in these animals.

Highlights

  • Very low density lipoprotein(VLDL)and low density lipoprotein (LDL) apoprotein-B turnover rates were measured simultaneouslyby injecting 1311-labeledVLDL and Iz5Ilabeled LDL into fasting baboons (Pupio sp.) selectively bred for high serum cholesterol levels and having either low or high LDL levels

  • very low density lipoproteins (VLDL) apolipoprotein B (apoB) production was not sufficient to account for LDL apoB production in high LDL animals, a finding that suggested that a large amount of LDL apoB was derived from a source other than VLDL apoB in these animals. -KKushwaha, R

  • Supplementary key words lipoproteins atherosclerosis lipoprotein metabolism Epidemiologic data from humans and experimental evidence from animal models have suggested that an elevated low density lipoprotein (LDL) concentration in plasma is a major cause of atherosclerosis [1,2,3,4,5]

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Summary

Introduction

Very low density lipoprotein(VLDL)and low density lipoprotein (LDL) apoprotein (apo)-B turnover rates were measured simultaneouslyby injecting 1311-labeledVLDL and Iz5Ilabeled LDL into fasting baboons (Pupio sp.) selectively bred for high serum cholesterol levels and having either low or high LDL levels. Supplementary key words lipoproteins atherosclerosis lipoprotein metabolism Epidemiologic data from humans and experimental evidence from animal models have suggested that an elevated low density lipoprotein (LDL) concentration in plasma is a major cause of atherosclerosis [1,2,3,4,5] Levels of these lipoproteins in the plasma vary considerably among humans and among experimental animals, even while they are consuming identical diets. The present studies were conducted to determine whether production, or catabolism, or both, of either VLDL or LDL apoB are responsible for the contrasting high and low plasma concentrations of LDL in selectively bred pedigreed baboons

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