Stroke, Vol 18, 512-518, Copyright © 1987 by American Heart Association
M Yokota, E Tani, Y Maeda and K Kokubu
Experimental delayed cerebral vasospasm was produced in canine basilar
arteries by 2 successive injections, 2 days apart, of fresh autogenous
arterial blood into the cisterna magna. When angiographic evidence of
delayed vasospasm was confirmed 7 days after the initial intracisternal
blood injection, a selective inhibitor of 5-lipoxygenase, 2-(12-
hydroxydodeca-5,10-diynyl)-3,5,6-trimethyl-1,4-benzoqu inone (AA-861), was
infused intravenously at 6.5 X 10(-4) mg/kg/min for 2 hours. However,
angiographic evidence of delayed vasospasm was not reversed, and mean
regional cerebral blood flow was not significantly increased. In other
studies, oral doses of AA-861 at 100 mg/kg/day were given twice a day for 7
days after the initial intracisternal blood injection. In the treated
group, angiographic evidence of delayed vasospasm was significantly
reduced, and the contractile property of excised basilar arteries in
response to vasoconstrictor agents was significantly improved. It is
suggested that leukotrienes, 5- lipoxygenase products of arachidonic acid,
might be important etiologic factors responsible for the development of
delayed vasospasm and that AA-861 would have a therapeutic effect not on
the reduction of delayed vasospasm once developed but on the prevention of
the development of delayed vasospasm.
ARTICLES
Effect of 5-lipoxygenase inhibitor on experimental delayed cerebral vasospasm
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