Simon R P, Chen J, Graham S H
Department of Neurology, University of California, San Francisco.
J Pharmacol Exp Ther. 1993 Apr;265(1):24-9.
The efficacy of GM1 ganglioside treatment in stroke was studied in a permanent middle cerebral artery occlusion model in the rat. A dose-dependent attenuation of infarct size at 24 hr was documented with the maximum effective dose halving the volume of the experimental stroke. Delayed administration at 5 min, but not 15 min, after vessel occlusion was as effective as preocclusion drug administration. Morphologic sparing was confined to the cortical penumbra; no protection in the ischemic core was found. Morphologically salvaged cortex was also metabolically preserved as demonstrated by quantitative measurement of glucose utilization. In vivo microdialysis demonstrated an attenuation of ischemic-induced glutamate release in the cortex with GM1 administration but no effect was found in the caudate. Hypotension did not occur even with doubling of the maximally effective dose of GM1. Accordingly, GM1 may be a safe and effective treatment for stroke.
在大鼠永久性大脑中动脉闭塞模型中研究了神经节苷脂GM1治疗中风的疗效。记录到在24小时时梗死面积呈剂量依赖性减小,最大有效剂量使实验性中风的体积减半。在血管闭塞后5分钟而非15分钟延迟给药与闭塞前给药效果相同。形态学上的挽救仅限于皮质半暗带;在缺血核心区未发现保护作用。通过葡萄糖利用的定量测量表明,形态学上挽救的皮质在代谢上也得以保留。体内微透析显示,给予GM1后皮质中缺血诱导的谷氨酸释放减少,但在尾状核中未发现影响。即使将GM1的最大有效剂量加倍也未出现低血压。因此,GM1可能是一种安全有效的中风治疗方法。