Lazarova M, Roussinov K
Acta Physiol Pharmacol Bulg. 1979;5(3):67-74.
Experiments with pentylenetetrazol convulsion model in albino mice--80 mg/kg subcutaneously--have revealed the following. The inhibitory effect of 5-HT, introduced intracerebroventricularly in a dose of 100 micrograms per mouse is eliminated by 500 mg/kg L-DOPA, 100 mg/kg amantadine, 5 mg/kg amphetamine and apomorphine, while for lower doses of the dopaminergic agent only a tendency towards antagonism is observed. The inhibitory effect of 50HTP in a dose of 200 mg/kg i. p. is eliminated by 500 mg/kg L-DOPA, 50 mg/kg amantadine and 5 mg/kg amphetamine, but it is not influenced by these drugs in doses of 250 mg/kg L-DOPA, 25 mg/kg amantadine and 5 mg/kg apomorphine, although when applied independently L-DOPA and amantadine in these lower doses potentiate convulsive reactions. The results obtained show that the dopaminergic and 5-HT-ergic systems have an antagonist effect on the convulsive reactivity in the case of pentylenetetrazol convulsion model. These results are in agreement with our views about the determining role of the balance between the various neurotransmitter systems in convulsive-seizure reactions.
对白化病小鼠进行的戊四氮惊厥模型实验(皮下注射80毫克/千克)显示了以下结果。每只小鼠脑室内注射100微克5-羟色胺的抑制作用可被500毫克/千克左旋多巴、100毫克/千克金刚烷胺、5毫克/千克苯丙胺和阿扑吗啡消除,而对于较低剂量的多巴胺能药物,仅观察到拮抗趋势。腹腔注射200毫克/千克5-羟色氨酸的抑制作用可被500毫克/千克左旋多巴、50毫克/千克金刚烷胺和5毫克/千克苯丙胺消除,但在250毫克/千克左旋多巴、25毫克/千克金刚烷胺和5毫克/千克阿扑吗啡剂量下不受这些药物影响,尽管单独使用这些较低剂量的左旋多巴和金刚烷胺会增强惊厥反应。所得结果表明,在戊四氮惊厥模型中,多巴胺能系统和5-羟色胺能系统对惊厥反应性具有拮抗作用。这些结果与我们关于各种神经递质系统之间平衡在惊厥发作反应中起决定性作用的观点一致。