Abstract

Inbred strains of mice with differing susceptibilities to atherosclerosis possess widely varying plasma HDL levels. Cholesterol absorption and lipoprotein formation were compared between atherosclerosis-susceptible, low-HDL C57BL6/J mice and atherosclerosis-resistant, high-HDL FVBN/J mice. [(3)H]cholesterol and triglyceride appeared in the plasma of FVB mice gavaged with cholesterol in olive oil at a much higher rate than in C57 mice. The plasma cholesterol was found almost entirely as HDL-cholesterol in both strains. Inhibition of lipoprotein catabolism with Tyloxapol revealed that the difference in the rate of [(3)H]cholesterol appearance in the plasma was due entirely to a greater rate of chylomicron secretion from the intestine of the FVB mice. Lipid absorption into the 2nd quarter of the small intestine is greater in the FVB mice and indicates that this region may contain the factors that give rise to the differences in absorption observed between the two mouse strains. Additionally, ad libitum feeding prior to cholesterol gavage accentuates the absorption rate differences compared with fasting. The resultant remodeling of the increased levels of chylomicron in the plasma may contribute to increased plasma HDL. Intestinal gene expression analysis reveals several genes that may play a role in these differences, including microsomal triglyceride transfer protein and ABCG8.

Highlights

  • Inbred strains of mice with differing susceptibilities to atherosclerosis possess widely varying plasma HDL levels

  • Several other strains of mice were tested, and the C57 mouse was found to have among the lowest rate of appearance of radiolabeled cholesterol in the plasma following gavage, whereas the FVB mouse was among the highest (Fig. 1C)

  • The existence of a variety of inbred mouse strains that possess a wide range of steady-state plasma cholesterol levels provides a useful tool in investigating the genetic causes

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Summary

Introduction

Inbred strains of mice with differing susceptibilities to atherosclerosis possess widely varying plasma HDL levels. We have recently studied the HDL levels, composition, and some properties of the particles derived from C57BL6 (C57) and FVB/N (FVB) mice [3] These strains differ in apoA-I (two amino acid differences) and apoA-II (three amino acid differences). The inbred mouse strains C57BL6 and FVB/N have been widely studied owing to their differing susceptibilities to atherosclerosis, the C57 being one of the most athero-susceptible mouse strains, whereas the FVB is highly resistant [4] These two mouse strains differ greatly in their plasma cholesterol levels, with wild-type FVB mice having HDL levels 2-fold higher than those of wild-type C57 mice. Crosses of mouse strains that vary in their cholesterol absorption efficiencies have shown that the genetic regulation is found at the enterocyte level [16, 17]. Other factors, including the rate of gastric emptying, have been shown to alter the rate of cholesterol absorption between inbred mouse strains [25]

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