OPIOID RECEPTOR ANTAGONIST NALMEFENE STEREOSPECIFICALLY INHIBITS GLUTAMATE RELEASE DURING GLOBAL CEREBRAL-ISCHEMIA

被引:16
作者
GRAHAM, SH
SHIMIZU, H
NEWMAN, A
WEINSTEIN, P
FADEN, AI
机构
[1] GEORGETOWN UNIV,SCH MED,DEPT NEUROL,WASHINGTON,DC 20007
[2] GEORGETOWN UNIV,SCH MED,DEPT PHARMACOL,WASHINGTON,DC 20007
[3] UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94121
[4] UNIV CALIF SAN FRANCISCO,DEPT NEUROSURG,SAN FRANCISCO,CA 94121
[5] WALTER REED ARMY INST RES,DEPT APPL BIOCHEM,WASHINGTON,DC 20307
关键词
OPIOID ANTAGONIST; MICRODIALYSIS; STROKE; EXCITATORY AMINO ACID;
D O I
10.1016/0006-8993(93)91175-R
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The opioid receptor antagonist nalmefene improves cellular bioenergetics and attenuates the reduction in tissue glutamate levels after global cerebral ischemia/reperfusion. The latter finding suggests that nalmefene might inhibit glutamate release during ischemia. To test this hypothesis, we used microdialysis techniques to examine the effect of nalmefene pretreatment on extracellular excitatory amino acid levels during global cerebral ischemia in rats. Saline, (-)-nalmefene (20, 100 or 500 mu g/kg) or the inactive nalmefene enantiomer (+)-nalmefene (100 mu g/kg) were given 15 min prior to induction of ischemia using a multi-vessel occlusion model. Pretreatment with (-)-nalmefene decreased peak dialysate glutamate in a dose-dependent fashion as compared to saline-treated controls, whereas (+)-nalmefene had no effect. These results suggest that opioid receptors may modulate glutamate release during ischemia and that inhibition of excitatory amino acid release may contribute to the protective actions of opioid receptor antagonists in cerebral ischemia.
引用
收藏
页码:346 / 350
页数:5
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