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(Arteriosclerosis, Thrombosis, and Vascular Biology. 2000;20:e26.)
© 2000 American Heart Association, Inc.

Atherosclerosis and Lipoproteins

Site-Specific Antiatherogenic Effect of Probucol in Apolipoprotein E–Deficient Mice

Paul K. Witting; Knut Pettersson; Jacinta Letters; Roland Stocker

From the Biochemistry Group (K.P., J.L., R.S.), The Heart Research Institute, Camperdown, Australia, and Cardiovascular Pharmacology (P.K.W.), AstraZeneca, Mölndal, Sweden. P.K.W. is presently at the Department of Biochemistry and Molecular Biology, University of Vancouver, Vancouver BC, Canada.

Correspondence to Roland Stocker, The Heart Research Institute, 145 Missenden Rd, Camperdown NSW 2050, Australia. E-mail r.stocker{at}hri.org.au

Abstract—The lipid-lowering antioxidant probucol can inhibit atherosclerosis in animals and restenosis in humans. However, probucol has been shown to promote atherosclerosis in the aortic root of apolipoprotein E–deficient (apoE-/-) mice. In the current study, we examined the effects of probucol on both lesion formation at 4 sites along the aorta and lipoprotein oxidation in the plasma and aortas of apoE-/- mice receiving a diet containing 21.2% (wt/wt) fat and 0.15% (wt/wt) cholesterol without or with 1% (wt/wt) probucol. After 6 months, controls had developed lesions at all sites investigated. Lesion development was strongly (P=0.0001) affected by probucol, but this effect was not uniform: lesion size was increased in the aortic root but significantly decreased in the arch, the descending thoracic aorta, and proximal abdominal aorta. Plasma and aortas of probucol-treated mice contained high concentrations of probucol and its metabolites (bisphenol and diphenoquinone); increased vitamin C; markedly decreased very low density lipoprotein (but not low density lipoprotein and high density lipoprotein); and decreased cholesterol, cholesteryl esters, triglycerides, vitamin E, and oxidized lipids compared with controls. Interestingly, probucol treatment did not decrease the proportion of aortic lipids that were oxidized. Plasma vitamin C and bisphenol, but not probucol, protected plasma lipids from ex vivo oxidation by peroxyl radicals. These results show that as in other species, probucol can inhibit lesion formation in most parts of the aorta of apoE-/- mice. This effect may involve lipid oxidation–independent mechanisms localized within the vessel wall as well as lipid lowering.

Key Words: ascorbate • atherogenesis • lipid peroxidation • lipoprotein oxidation • probucol

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