Ochiai C, Asano T, Takakura K, Fukuda T, Horizoe H, Morimoto Y
Stroke. 1982 Nov-Dec;13(6):788-96. doi: 10.1161/01.str.13.6.788.
The effects of delayed administration of pentobarbital and a novel imidazole derivative (Nizofenone or Y-9179) on the infarction size following the regional cerebral ischemia were studied using the permanent middle cerebral artery (MCA) occlusion model in cats. The courses of local cerebral blood flow (lCBF) before and after drug administration were also studied using the hydrogen clearance method. The extent of infarction one week after MCA occlusion was significantly smaller in the drug-treated groups than in the control group. Regarding the time-course of lCBF, there was no significant differences between the control and the Y-9179 groups. On the other hand, pentobarbital administration caused a significant lCBF increase in low-flow areas where the lCBF following MCA occlusion was below 40 ml/100g/min. In spite of this flow increase, the corresponding cortical areas underwent infarction. Histological examination of the state of vasogenic edema revealed that the perivascular exudation of plasma fluid in the infarcted area was definitely less in the Y-9179 treated group than in the other groups. Results indicate that redistribution of lCBF may not be involved in the mechanism of cerebral protection by pentobarbital or Y-9179.
采用猫永久性大脑中动脉(MCA)闭塞模型,研究了戊巴比妥和新型咪唑衍生物(尼唑苯酮或Y-9179)延迟给药对局部脑缺血后梗死面积的影响。还采用氢清除法研究了给药前后局部脑血流量(lCBF)的变化过程。MCA闭塞一周后,药物治疗组的梗死范围明显小于对照组。关于lCBF的时间进程,对照组和Y-9179组之间没有显著差异。另一方面,戊巴比妥给药使MCA闭塞后lCBF低于40 ml/100g/min的低血流区域的lCBF显著增加。尽管血流量增加,但相应的皮质区域仍发生梗死。对血管源性水肿状态的组织学检查显示,Y-9179治疗组梗死区域血管周围血浆液体的渗出明显少于其他组。结果表明,lCBF的重新分布可能不参与戊巴比妥或Y-9179的脑保护机制。