Stroke, Vol 20, 501-506, Copyright © 1989 by American Heart Association
T Ueda, YL Yamamoto and M Diksic
We report on the effect of calcium channel blocker verapamil administered
into the inferior cerebral vein in rats 1 hour after occlusion of the
middle cerebral artery. Twenty-four rats were divided into four groups of
six rats each. Group A rats received no medication. The other three groups
received 0.1 mg verapamil/kg/2 hr. Group B rats received verapamil
intravenously. Group C and D rats received verapamil and autologous
arterial blood by transvenous perfusion of the brain, Group C rats at 100
mm Hg perfusion pressure and Group D rats at 150 mm Hg perfusion pressure.
The administration of verapamil started 1 hour after middle cerebral artery
occlusion and lasted for 2 hours. Three hours after occlusion, we used
double- or single-tracer autoradiography with 4-[18F]fluoroantipyrine or
[14C]iodoantipyrine and [14C]alpha- aminoisobutyric acid as tracers to
study the brains for local cerebral blood flow and blood-brain barrier
permeability changes. Group C showed a significant increase of local
cerebral blood flow in the parietal cortex (89%, p less than 0.01) and
sensorimotor cortex (64%, p less than 0.05) compared with Group A. Group D
showed an extensive and striking increase in local cerebral blood flow of
the ischemic cortical and subcortical areas (57-100%, p less than 0.05).
Group B showed no significant changes but exhibited further reduction of
local cerebral blood flow in the ischemic cerebral hemisphere associated
with slightly increased local cerebral blood flow in the nonischemic
cerebral hemisphere compared with Group A. There was no change of
blood-brain barrier permeability in any group.(ABSTRACT TRUNCATED AT 250
WORDS)
ARTICLES
Transvenous perfusion of the brain with verapamil during focal cerebral ischemia in rats
Cone Neurosurgical Research Laboratory, Montreal Neurological Institute, McGill University, Canada.
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