Stroke, Vol 25, 481-485, Copyright © 1994 by American Heart Association
K Takagi, MD Ginsberg, MY Globus, R Busto and WD Dietrich
BACKGROUND AND PURPOSE: In a previous study from our laboratory,
ritanserin, a specific 5-HT2 serotonin receptor antagonist, reduced
ischemic damage in the setting of transient global ischemia. In this study,
we examined the effect of ritanserin on ischemic cerebral blood flow,
systemic blood pressure, and infarct volume in the model of permanent focal
ischemia with brain temperature controlled at 35.0 degrees C to 36.0
degrees C. METHODS: Thirty-seven male Sprague-Dawley rats were used. The
right middle cerebral artery was permanently occluded. Ritanserin (8 mg/kg)
or vehicle was continuously administered intravenously for 90 minutes
starting 10 minutes after middle cerebral artery occlusion. Cerebral blood
flow was monitored by laser Doppler flowmetry in the ischemic cortex before
and for 2 hours after arterial occlusion. Brains were perfusion-fixed 3
days later, and infarct volumes were measured. RESULTS: Mean arterial blood
pressure was not affected by treatment. In the vehicle and ritanserin
groups, mean ischemic cerebral blood flow (percent of preischemic values)
was 34.6 +/- 14.7% (mean +/- SD) and 26.6 +/- 15.0%, respectively.
Hemispheric infarct volumes were 119.3 +/- 49.4 mm3 and 136.6 +/- 49.6 mm3,
respectively. No significant differences were recognized. CONCLUSIONS:
Intravenous administration of ritanserin did not affect mean arterial blood
pressure or cerebral blood flow in the ischemic region during the acute
phase of ischemia. No protective effect of ritanserin was apparent in the
setting of permanent focal ischemia when treatment was begun shortly after
the onset of ischemia.
ARTICLES
The effect of ritanserin, a 5-HT2 receptor antagonist, on ischemic cerebral blood flow and infarct volume in rat middle cerebral artery occlusion
Department of Neurology, University of Miami School of Medicine, FL 33101.
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