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Neither antioxidants nor genistein inhibit the progression of established atherosclerotic lesions in older apoE deficient mice
- Publication Year :
- 2009
- Publisher :
- Elsevier Science Ireland Limited:PO Box 85, Limerick Ireland:011 353 61 709600, 011 353 61 61944, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 353 61 709114, 2009.
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Abstract
- Supplements and diets enriched in antioxidants and soy isoflavones are purported to reduce cardiovascular disease risk. Many experimental studies have demonstrated inhibitory effects of antioxidants and soy isoflavones on the development of fatty streaks in animal models. However, it is still unknown whether antioxidants and isoflavones have comparable inhibitory effects on the progression of advanced stages of atherosclerosis. This is an important question because clinical trials in humans have not supported a cardio-protective role for antioxidants or isoflavones. Thus, we examined the effects of antioxidants and genistein on the progression and composition of established, advanced atherosclerotic lesions in the innominate arteries (IA) of older apolipoprotein E-deficient (apoE(-/-)) mice. Thirty-week-old male apoE(-/-) mice were fed chow with or without genistein (0.27%, w/w) for 6, 12 and 24 weeks. Twenty-week-old male apoE(-/-) mice were fed chow with or without a cocktail of antioxidants (vitamin E 0.2%, w/w; vitamin C 0.05%, w/w; and beta carotene 0.5%, w/w) for 10, 16, and 22 weeks. There were no significant differences in total plasma cholesterol, body weight, average lesion or medial area, or changes in lesion composition with either treatment in comparison to control mice.
- Subjects :
- Apolipoprotein E
medicine.medical_specialty
Vitamin C
Apolipoprotein B
Cholesterol
Vitamin E
medicine.medical_treatment
Genistein
Biology
Isoflavones
Lesion
chemistry.chemical_compound
Endocrinology
chemistry
Internal medicine
medicine
biology.protein
medicine.symptom
Cardiology and Cardiovascular Medicine
Subjects
Details
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....21bd7a27a7d87a5366a62fd2b6c1ded2