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自由基捕获剂4-[(叔丁基亚氨基)甲基]苯-1,3-二磺酸钠N-氧化物(NXY-059)在大鼠出血性中风模型中的疗效

Efficacy of disodium 4-[(tert-butylimino)methyl]benzene-1,3-disulfonate N-oxide (NXY-059), a free radical trapping agent, in a rat model of hemorrhagic stroke.

作者信息

Peeling J, Del Bigio M R, Corbett D, Green A R, Jackson D M

机构信息

Department of Pharmacology and Therapeutics, The University of Manitoba, 770 Bannatyne Avenue, R3E 0W3, Winnipeg, MN, Canada.

出版信息

Neuropharmacology. 2001 Mar;40(3):433-9. doi: 10.1016/s0028-3908(00)00170-2.

DOI:10.1016/s0028-3908(00)00170-2
PMID:11166336
Abstract

Because free radical mechanisms may contribute to brain injury in hemorrhagic stroke, the effect of the free radical trapping agent disodium 4-[(tert-butylimino)methyl]benzene-1,3-disulfonate N-oxide (NXY-059) was investigated on outcome following intracerebral hemorrhage (ICH) in rat. ICH was induced in 20 adult rats by infusion of collagenase into the caudate-putamen. Thirty minutes later rats were treated with NXY-059 (50 mg/kg subcutaneous plus 8.8 mg/kg/h for 3 days subcutaneous delivered via implanted osmotic pumps) or saline (equivalent volumes). Magnetic resonance imaging 24 h after ICH confirmed that the hemorrhage was uniform in the two groups, and subsequent imaging at 7 and 42 days post-ICH showed that the hematoma resolved similarly in the two groups. Behavioral testing on days 1, 3, 7, 14, and 21 after ICH showed that rats treated with NXY-059 had significantly decreased neurological impairment at all times. Deficits in skilled forelimb use 4-5 weeks post-ICH, and in striatal function 6 weeks post-ICH, were not reduced by treatment with NXY-059. Treatment with NXY-059 significantly reduced the neutrophil infiltrate observed 48 h post-hemorrhage in the vicinity of the hematoma, and the number of TUNEL-positive cells 48 h post-hemorrhage at the hematoma margin. However, by 6 weeks there were no differences in neuronal densities in treated and control rats.

摘要

由于自由基机制可能导致出血性中风中的脑损伤,因此研究了自由基捕获剂4-[(叔丁基亚氨基)甲基]苯-1,3-二磺酸钠N-氧化物(NXY-059)对大鼠脑出血(ICH)后结局的影响。通过向尾状核-壳核注入胶原酶,在20只成年大鼠中诱导脑出血。30分钟后,用NXY-059(50mg/kg皮下注射加8.8mg/kg/h,通过植入的渗透泵皮下给药3天)或生理盐水(等体积)治疗大鼠。脑出血后24小时的磁共振成像证实两组出血均匀,脑出血后7天和42天的后续成像显示两组血肿消退情况相似。脑出血后第1、3、7、14和21天的行为测试表明,用NXY-059治疗的大鼠在所有时间点的神经功能缺损均显著降低。脑出血后4-5周熟练前肢使用的缺陷以及脑出血后6周纹状体功能的缺陷,并未因NXY-059治疗而减轻。NXY-059治疗显著减少了脑出血后48小时在血肿附近观察到的中性粒细胞浸润以及血肿边缘脑出血后48小时TUNEL阳性细胞的数量。然而,到6周时,治疗组和对照组大鼠的神经元密度没有差异。

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