EXCITATORY AMINO-ACID ANTAGONISTS AND PENTYLENETETRAZOL-INDUCED SEIZURES DURING ONTOGENY .2. THE EFFECTS OF MK-801

被引:44
作者
VELISEK, L
VERESOVA, S
POBISOVA, H
MARES, P
机构
[1] Institute of Physiology, Czechoslovak Academy of Sciences, Prague 4, CS-142 20
关键词
PENTYLENETETRAZOL; MK-801; RAT; SEIZURE; ONTOGENY;
D O I
10.1007/BF02245658
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
MK-801 is a non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist with anticonvulsant and neuroprotective properties. The action of MK-801 (0.05-10 mg/kg IP) was assessed against pentylenetetrazol-induced seizures (PTZ; 100 mg/kg SC; 30 min after MK-801) in rats aged 7, 12, 18, 25, and 90 days (N = 263). We observed pronounced ataxia and hypermobility after MK-801 pretreatment during the whole ontogenesis, and the animals exhibited head-weaving and body-rolls. After the combination of MK-801 and PTZ "wet dog shakes" were detected in 18-, 25-, and 90-day-old rats (never seen in controls receiving PTZ only). MK-801 only insignificantly modified the latencies of minimal (clonic) seizures in 18-day-old and older rats where this seizure type is regularly elicited. In 12-day-old rats an increased incidence of minimal seizures was detected. MK-801 nearly completely blocked or strongly delayed major (generalized tonic-clonic) seizures and attenuated the seizure severity during ontogenesis in a dose-dependent manner. Present results suggest the important role of NMDA receptors in the genesis of generalized tonic-clonic seizures whilst the role of NMDA receptors in minimal seizures appears to be negligible during the whole ontogenetic development.
引用
收藏
页码:510 / 514
页数:5
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