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Journal of Lipid Research, Vol. 47, 476-483, March 2006
Copyright © 2006 by American Society for Biochemistry and Molecular Biology



* Department of Pharmacology, Berlex Bioscience, Richmond, CA
Department of Internal Medicine, School of Medicine, University of California at Davis, Davis, CA
Department of Pathology, Microbiology, and Immunology, School of Veterinary Medicine, University of California at Davis, Davis, CA
Published, JLR Papers in Press, December 21, 2005.
1 To whom correspondence should be addressed. e-mail: valdeci_dacunha{at}yahoo.com
Two month old C57BL/6 mice were placed on three different diets: 1) normal diet (NC; 0.025% cholesterol), 2) hypercholesterolemic Western-type diet (HC-W; 0.2% cholesterol), and 3) hypercholesterolemic Paigen-type diet (HC-P; 1.25% cholesterol plus 0.5% cholic acid). At 6 months of age, the animals underwent ligation of the left carotid artery and were randomly assigned to vehicle (PBS, subcutaneous) or angiotensin II (Ang II; 1.4 mg/kg/day, subcutaneous) treatment for 4 weeks. Low density lipoprotein-cholesterol levels were similarly increased in both HC diets (NC, 4 ± 3 mg/dl; HC-W, 123 ± 17 mg/dl; HC-P, 160 ± 14 mg/dl). However, the levels of high density lipoprotein-cholesterol (HDL-C) were reduced only in animals fed the HC-P diet (NC, 82 ± 6 mg/dl; HC-W, 79 ± 7 mg/dl; HC-P, 58 ± 7 mg/dl). In Ang II-treated mice, carotid artery ligation induced intimal smooth muscle cell proliferation to a similar extent in NC- and HP-W-fed animals. However, a significantly larger intimal area developed in ligated vessels from Ang II-treated mice fed the HC-P diet (3.6-fold higher than in Ang II-treated NC mice). Together, these results show the accelerating effect of mild hypercholesterolemia, reduced HDL-C levels, and Ang II on intimal hyperplasia after carotid artery ligation in mice.
Supplementary key words high density lipoprotein smooth muscle cells vascular remodeling
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