NXY-059, a novel free radical trapping compound, reduces cortical infarction after permanent focal cerebral ischemia in the rat

被引:85
作者
Zhao, ZG
Cheng, MS
Maples, KR
Ma, JY
Buchan, AM
机构
[1] Univ Calgary, Alberta Stroke Program, Dept Clin Neurosci, Foothills Hosp, Calgary, AB T2N 2T9, Canada
[2] Centaur Pharmaceut Inc, Sunnyvale, CA 94085 USA
关键词
permanent focal ischemia; neuroprotection; free radical; rat; NXY-059;
D O I
10.1016/S0006-8993(01)02618-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Free radicals have gained wide acceptance as mediators of cerebral ischemic injury. It has previously been reported that a spin trap nitrone. alpha -phenyl-N-tert-butyl nitrone (PBN), can reduce infarct volumes in rats subjected to either permanent or transient focal cerebral ischemia. A recent study has demonstrated that NXY-059, a novel free radical trapping nitrone compound, has a neuroprotective effect against transient focal cerebral ischemia. This study was designed to determine the effect of NXY-059 in a rodent model of permanent focal cerebral ischemia. Male spontaneously hypertensive rats were subjected to permanent middle cerebral artery occlusion (MCAO) by placement of a microaneurysm clip on the middle cerebral artery (MCA). Animals were divided into three groups: (1) physiological saline given as a 1 ml/kg i.v. bolus administered 5 min post MCAO followed immediately by a continuous i.v. infusion of 0.5 ml/h of physiological saline for 24 h (n=10); (2) 30 mg/kg, 1 ml/kg, i.v. bolus of NXY-059 dissolved in physiological saline administered 5 min post MCAO followed immediately by a continuous i.v. infusion of 30 mg/kg/h, 0.5 ml/h, of NXY-059 for 24 h (n=9); (3) 60 mg/kg, 1 ml/kg, i.v. bolus of NXY-059 dissolved in physiological saline administered 5 min post MCAO followed immediately by a continuous i.v. infusion of 60 mg/kg/h, 0.5 ml/h, of NXY-059 for 24 h (n=12). Infarction was quantified after a survival period of 24 h. Differences in infarct volume were examined with one-way ANOVA following Dunnet's multiple comparison test. The percentage of cortical infarction in the saline control group was 22.6+/-6.8% (mean+/-S.D.) of contra-lateral hemisphere, and in the 30 mg/kg/h NXY-059-treated group was 17.4%+/-6.8% (NS). Plasma concentration (muM/l) of NXY-059 in the 30 mg/kg/h group was 80.2+/-52.2 (n=9), while in the 60 mg/kg/h group plasma concentration (muM/l) of NXY-059 was 391.0+/-207.0 (n=10). Infarction in the 60 mg/kg/h NXY-059-treated group was significantly reduced (P=0.009) to 14.5+/-5%. Our preliminary data demonstrate that administration of NXY-059 (60 mg/kg/h for 24 h) ameliorates cortical infarction in rats subjected to permanent focal cerebral ischemia with 24 h survival. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:46 / 50
页数:5
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