THE EFFECT OF A PLATELET-ACTIVATING-FACTOR ANTAGONIST (BN-52021) ON NEUROLOGIC OUTCOME AND HISTOPATHOLOGY IN A CANINE MODEL OF COMPLETE CEREBRAL-ISCHEMIA
Re. Hofer et al., THE EFFECT OF A PLATELET-ACTIVATING-FACTOR ANTAGONIST (BN-52021) ON NEUROLOGIC OUTCOME AND HISTOPATHOLOGY IN A CANINE MODEL OF COMPLETE CEREBRAL-ISCHEMIA, Anesthesiology, 79(2), 1993, pp. 347-353
Background. Research has demonstrated that platelet activating factor
may modulate, in part, the severity of postischemic neurologic injury.
The proposed mechanism involves a platelet activating factor-mediated
release of cerebral cellular lipids and free fatty acids, resulting i
n increased cerebral edema and cell injury. The present study tested t
he hypothesis that a specific platelet activating factor antagonist, B
N 52021, would improve neurologic outcome after 12 min of complete glo
bal cerebral ischemia in a canine model. Methods: Using an established
canine model of complete cerebral ischemia, dogs were assigned random
ly to receive, in a blinded fashion, either 20 mg/kg BN 52021 intraven
ously (N = 8) or placebo (N = 7) 5 min before cerebral ischemia. After
cerebral ischemia and recovery, neurologic assessment was performed b
y a blinded observer for 72 h. Immediately thereafter, the brains were
harvested and later were evaluated histologically by a neuropathologi
st blinded to the treatment groups. Results: Dogs were well matched fo
r systemic physiologic variables during all portions of the study. One
placebo-treated dog and one BN 52021-treated dog were not included in
the statistical analysis because of failure to meet preestablished pr
otocol criteria. BN 52021, when compared to placebo, affected neither
neurologic functional recovery nor overall histopathology scores. Regi
onal histopathology was improved in BN 52021-treated dogs in only 1 of
18 brain regions studied (i.e., the parietal cortex). When both treat
ment groups were combined, there was a significant correlation between
neurologic function rank and histopathology rank. Conclusions. The pr
esent data demonstrate that the platelet activating factor antagonist
BN 52021, at a dose of 20 mg/kg intravenously given 5 min before cereb
ral ischemia, did not protect the brain from injury in this canine mod
el of complete global ischemia.