Czuczwar S J, Turski L, Turski W, Kleinrok Z
Epilepsia. 1981 Aug;22(4):407-14. doi: 10.1111/j.1528-1157.1981.tb06151.x.
Mice were injected with intracerebroventricular (i.c.v.) kainic acid (KA; 0.1 micrograms per animal) and the pentetrazol test was carried out on the fifth day after the administration of the amino acid. The following antiepileptic drugs were tested for anticonvulsant activity in mice lesioned with KA: diazepam (0.4 mg/kg), phenobarbital (12.5 and 25 mg/kg), trimethadione (200 and 400 mg/kg), depakine (200 and 400 mg/kg), carbamazepine (10 and 20 mg/kg), lefadol (bromophenylsuccinimide; 20 mg/kg), and acetazolamide (320 mg/kg). All drugs were given intraperitoneally, except for carbamazepine, which was also given orally in doses of 100 and 200 mg/kg. Pentetrazol was administered subcutaneously in a dose of 110 mg/kg, and the animals were subsequently observed for the occurrence of clonic and tonic convulsions within 30 min. The protective effects of diazepam and phenobarbital were significantly reduced in the KA-lesioned animals, while the actions of the remaining anticonvulsants were unaltered. Moreover, a substantial loss of pyramidal cells in the CA 3 field of the hippocampus was noted after i.c.v. injection of KA. It may therefore be concluded that the mechanism of the action of diazepam and phenobarbital are partially dependent on the intact functions of the hippocampal formation.
给小鼠脑室内注射(i.c.v.)海藻酸(KA;每只动物0.1微克),并在给予该氨基酸后的第五天进行戊四氮试验。测试了以下抗癫痫药物对KA损伤小鼠的抗惊厥活性:地西泮(0.4毫克/千克)、苯巴比妥(12.5和25毫克/千克)、三甲双酮(200和400毫克/千克)、丙戊酸(200和400毫克/千克)、卡马西平(10和20毫克/千克)、左法朵(溴苯基琥珀酰亚胺;20毫克/千克)和乙酰唑胺(320毫克/千克)。除卡马西平外,所有药物均腹腔注射,卡马西平还口服给药,剂量为100和200毫克/千克。皮下注射戊四氮,剂量为110毫克/千克,随后观察动物在30分钟内是否出现阵挛性和强直性惊厥。在KA损伤的动物中,地西泮和苯巴比妥的保护作用显著降低,而其余抗惊厥药物的作用未改变。此外,脑室内注射KA后,海马CA 3区的锥体细胞大量丢失。因此可以得出结论,地西泮和苯巴比妥的作用机制部分依赖于海马结构的完整功能。