Quantitative assessment of aortic atherosclerosis in APOE*3 leiden transgenic mice and its relationship to serum cholesterol exposure

Pieter H.E. Groot*, Bart J.M. Van Vlijmen, G. Martin Benson, Marten H. Hofker, Raymond Schiffelers, Martin Vidgeon-Hart, Louis M. Havekes

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Transgenic mice overexpressing the human dysfunctional apolipoprotein E variant, APOE*3 Leiden, develop hyperlipidemia and are highly susceptible to diet-induced atherosclerosis. In the present study, we investigated the effects of diet composition and feeding period on serum cholesterol exposure and the amount of atherosclerosis in the aortic sinus in these mice, using quantitative image analysis. On each of the three diets tested-a low-fat diet, a high-saturated-fat/cholesterol diet, and a high saturated-fat/high- cholesterol/0.5%-cholate diet-transgenic animals showed a marked hyperlipidemia compared with nontransgenic littermates. Measurement of the atherosclerotic lesion areas in cross sections of the aortic sinus in animals exposed to these three diets for up to 6 months showed a 5 to 10 times greater lesion area in transgenic mice compared with nontransgenic controls. Highly significant positive correlations were found between the log-transformed data on lesion area and serum cholesterol exposure (r=.82 to .85 for the 1-, 2-, and 3-month treatment groups), indicating that the hyperlipidemia is likely to be a major determinant in lesion formation. On the basis of these findings, we suggest that the APOE*3 Leiden mouse represents a promising model for intervention studies with hypolipidemic and antiatherosclerotic drugs.

Original languageEnglish
Article numberdoi: 10.1161/01.atv.16.8.926
Pages (from-to)926-933
Number of pages8
JournalArteriosclerosis, Thrombosis and Vascular Biology
Volume16
Issue number8
DOIs
Publication statusPublished - 1996
Externally publishedYes

Keywords

  • animal model
  • apolipoprotein E
  • diet
  • familial dyslipoproteinemia
  • hyperlipidemia

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