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Updated: Jul 12, 2026

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Quantification of Atherosclerosis in Mice
Published on: June 12, 2019
Red wine does not reduce mature atherosclerosis in apolipoprotein E-deficient mice
J F Bentzon1, E Skovenborg, C Hansen
1Department of Cardiology and Institute of Experimental Clinical Research, Aarhus University Hospital, Denmark. jab@studmed.au.dk
Circulation
|March 29, 2001
Summary
Red wine polyphenols and ethanol did not reduce advanced atherosclerosis or alter plaque stability in mice. These findings suggest that moderate consumption may not protect against mature cardiovascular disease.
Area of Science:
- Cardiovascular Research
- Nutritional Science
- Pharmacology
Background:
- Red wine polyphenols and ethanol are known to reduce early atherosclerosis (fatty streaks) in animal models.
- This protective effect on early lesions supports epidemiological observations of reduced myocardial infarction in humans consuming alcoholic beverages.
- However, fatty streaks may not accurately represent advanced, clinically relevant atherosclerosis.
Purpose of the Study:
- To investigate the effects of red wine polyphenols and ethanol on mature atherosclerosis.
- To determine if these substances impact plaque stability in advanced atherosclerotic lesions.
Main Methods:
- Apolipoprotein E-deficient mice were used to model advanced atherosclerosis.
- Mice received water, red wine, ethanol, or red wine powder for 19 weeks.
- Atherosclerosis progression and plaque stability (collagen content) were assessed at study termination.
Main Results:
- HDL cholesterol levels were significantly increased by both red wine and ethanol consumption.
- No significant differences in the extent of mature atherosclerosis were observed in the aortic bulb or brachiocephalic trunk across all treatment groups.
- The collagen content within atherosclerotic plaques, an indicator of stability, did not differ among the groups.
Conclusions:
- Neither ethanol nor red wine polyphenols demonstrated a capacity to reduce mature atherosclerosis in this mouse model.
- These interventions did not alter the collagen content of atherosclerotic plaques, suggesting no effect on plaque stability.

