Stroke, Vol 22, 1562-1566, Copyright © 1991 by American Heart Association
T Hosaka, YL Yamamoto and M Diksic
BACKGROUND AND PURPOSE: For treatment of acute stroke, drug therapy
administered systemically has been unreliable due to inadequate delivery of
drug into ischemic tissue. We have developed a new method to deliver drugs
into the ischemic tissue by retrograde perfusion of the cerebral vein.
METHODS: We examined in rats the effectiveness of administering verapamil
into ischemic tissue by retrograde perfusion through the cerebral vein,
starting 3 hours after occlusion of the middle cerebral artery. Twenty-four
Fischer-344 rats with occlusion of the middle cerebral artery were divided
into four groups of six rats each. Group A rats had no treatment, group B
rats received verapamil intravenously, and groups C and D rats received
verapamil by transvenous perfusion of the brain with blood and with saline,
respectively. We studied local cerebral blood flow using the
autoradiographic method with carbon-14-labeled iodoantipyrine and examined
cerebral infarct volume with cresyl violet and Luxol fast blue staining.
RESULTS: As compared with group A rats, in groups C and D rats we found a
significant and extensive increase of cerebral blood flow in the ischemic
cortical and subcortical areas (55-119%, p less than 0.05) and a
significant reduction of cerebral infarct volume (31- 39%, p less than
0.05). We found no significant changes in group B rats. CONCLUSIONS: This
study shows that transvenous perfusion of the brain with verapamil starting
3 hours after occlusion of the middle cerebral artery produces a
significantly beneficial effect in rats.
ARTICLES
Efficacy of retrograde perfusion of the cerebral vein with verapamil after focal ischemia in rat brain
Cone Neurosurgical Research Laboratory, Montreal Neurological Institute, McGill University, Quebec, Canada.
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