The neuroprotective effect of chlormethiazole on ischaemic neuronal damage following permanent middle cerebral artery ischaemia in the rat

Simon G Sydserff, Alan J Cross, A.Richard Green
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引用次数: 68

Abstract

The ability of chloremethiazole to protect against ischaemic cell damage in a rat model of permanent focal ischaemia has been examined. Chlormethiazole (1 mmol/kg) was administered intraperitoneally either 1 or 3 h after occlusion of the middle cerebral artery with an intraluminal filament. Twenty four hours after the start of occlusion there was histological evidence for ischaemic damage in both cortex and striatum. The volume of ischaemic damage in control (saline injected) animals was 310 ± 25 mm3 (mean ± SEM; n = 6). Chlormethiazole administered 1 h after occlusion reduced this damage by 58% (128 ± 40 mm3; n = 6; P < 0.01), protection being observed in both brain regions. The drug was ineffective when given 3 h after occlusion (304 ± 25 mm3; n = 5). Chlormethiazole had no effect on body temperature, mean arterial blood pressure, blood pH, pO2 or pCO2, but did induce mild bradycardia. Chlormethiazole therefore appears to be an effective neuroprotective agent in this model of permanent ischaemia, complementing previous data on the efficacy of this drug in other focal and global models of cerebral ischaemia.

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氯甲唑对大鼠永久性大脑中动脉缺血后缺血性神经元损伤的神经保护作用
研究了氯甲咪唑对永久性局灶性缺血大鼠模型中缺血细胞损伤的保护作用。用腔内细丝封堵大脑中动脉后1或3小时,腹腔注射氯甲基唑(1 mmol/kg)。阻断开始24小时后,皮层和纹状体均有缺血损伤的组织学证据。对照组(注射生理盐水)动物缺血损伤体积为310±25 mm3(平均±SEM;n = 6)。闭塞后1小时给予氯甲唑可使该损伤减少58%(128±40 mm3;N = 6;P & lt;0.01),在两个脑区都观察到保护作用。闭塞后3 h给药无效(304±25 mm3;n = 5)。氯甲唑对体温、平均动脉血压、血液pH、pO2、pCO2均无影响,但可引起轻度心动过缓。因此,氯甲基唑在这种永久性缺血模型中似乎是一种有效的神经保护剂,补充了先前关于该药物在其他局灶性和全局性脑缺血模型中的疗效的数据。
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