Velísek L, Mikolásová R, Blanková-Vanková S, Mares P
Institute of Physiology, Czechoslovak Academy of Sciences, Prague.
Pharmacol Biochem Behav. 1989 Feb;32(2):405-10. doi: 10.1016/0091-3057(89)90170-6.
An anticonvulsant action of ketamine, a noncompetitive NMDA receptor antagonist (1-40 mg/kg IP), on the metrazol-induced seizures was assessed in male Wistar rats aged 7, 12, 18, 25 and 90 days. Ketamine alone caused ataxia even in the lowest dose used. As concerens its interaction with metrazol it exerted a clearcut anticonvulsant effect against generalized tonic-clonic seizures at all developmental stages. On the contrary, the effects on clonic (i.e., minimal) seizures were only moderate or absent. Higher efficacy of ketamine was observed in young animals. Our results suggest a role of excitatory amino acids in the generation of generalized tonic-clonic metrazol seizures, but their share on the induction of clonic (minimal) seizures seems to be very small.
在7、12、18、25和90日龄的雄性Wistar大鼠中,评估了非竞争性NMDA受体拮抗剂氯胺酮(腹腔注射剂量为1 - 40毫克/千克)对戊四氮诱发癫痫发作的抗惊厥作用。单独使用氯胺酮即使在最低剂量时也会引起共济失调。关于其与戊四氮的相互作用,在所有发育阶段,它对全身强直阵挛性发作均有明显的抗惊厥作用。相反,对阵挛性(即轻微)发作的作用仅为中等程度或无作用。在幼龄动物中观察到氯胺酮的疗效更高。我们的结果表明,兴奋性氨基酸在全身强直阵挛性戊四氮癫痫发作的产生中起作用,但它们在阵挛性(轻微)发作诱导中的作用似乎非常小。