Stroke, Vol 13, 302-307, Copyright © 1982 by American Heart Association
JR Little, JP Latchaw Jr, RM Slugg, RP Lesser and NT Stowe
Propranolol has been found to have a protective effect in experimental
myocardial ischemia. Protection of ischemic kidneys was subsequently
demonstrated following treatment with propranolol and its weaker beta
blocking isomer, d-propranolol. The objective of the present investigation
was to study the effects of propranolol (i.e., racemic d,1 mixture) and
d-propranolol upon regional cerebral blood flow (rCBF) and early ischemic
changes following experimental middle cerebral artery (MCA) occlusion.
Thirty adult cats, lightly anesthetized with ketamine hydrochloride,
underwent 3 hours or right MCA occlusion. Ten cats were untreated. Ten cats
were given a continuous infusion of propranolol (1 mg/kg/hr) for 4 hours
beginning 1 hour before MCA occlusion and a 4 mg/kg bolus immediately
before occlusion. Ten cats were given a continuous infusion of
d-propranolol (0.5 mg/kg/hr) for 4 hours beginning 1 hour before MCA
occlusion and a 2 mg/kg bolus immediately before occlusion. The therapeutic
agents were injected directly into the right carotid artery. The rCBF in
the right Sylvian region was not significantly different in the 3 groups.
EEG changes also were similar. Carbon filling defects were found to be
smallest in the d-propranolol-treated group. Light microscopic studies
demonstrated a reduction in infarct size in the propranolol and
d-propranolol groups. The findings of the investigation indicated that
propranolol and d-propranolol do not have a deleterious effect on rCBF
after MCA occlusion and suggested that these agents have a protective
effect upon ischemic cerebral tissue.
ARTICLES
Treatment of acute focal cerebral ischemia with propranolol
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