Circulation, Vol 66, 338-341, Copyright © 1982 by American Heart Association
LI Bonchek, LE Boerboom, GN Olinger, JR Pepper, J Munns, L Hutchinson and AH Kissebah
The ameliorative effect of antiplatelet therapy on atherogenesis of vein
grafts was assessed in autologous cephalic veins grafted into femoral
arteries of 16 normolipemic and 11 hyperlipemic stump-tailed macaque
monkeys. Before grafting, one half of each vein was distended at high
pressure (700 mm Hg) and the other half at low pressure (350 mm Hg). Eight
normolipemic monkeys were treated with aspirin, 80 mg/day, and
dipyridamole, 50 mg/day, and eight were controls. When grafts were
harvested at 12 weeks, tissue cholesterol and beta-apoprotein content in
grafts from untreated monkeys were significantly higher than in ungrafted,
uninjured veins. Antiplatelet therapy eliminated the increase in lipid
content of vein segments distended at low pressure, and significantly
lowered lipid content of segments distended at high pressure, though not to
be control levels of ungrafted veins. Seven of the 11 hyperlipemic monkeys
received antiplatelet drugs and four did not. The lipid content of all
graft segments was significantly higher than in grafted or ungrafted veins
from normolipemic monkeys. Antiplatelet therapy again significantly reduced
the lipid content in vein segments distended at both levels of pressure,
and also reduced the elevated cholesterol content in ungrafted veins.
Although this animal preparation differs in many ways from human coronary
bypass operations, these observations may be pertinent to the prevention of
atherosclerosis in human vein bypass grafts.
ARTICLES
Prevention of lipid accumulation in experimental vein bypass grafts by antiplatelet therapy
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