Mares P, Mirvaldová H, Bĕlská M
Institute of Physiology, Czechoslovak Academy of Sciences, Prague.
Physiol Bohemoslov. 1990;39(3):199-205.
The anticonvulsant action of a new antiepileptic drug ORG 6370 (Organon International B.V.) was studied in 217 male albino rats aged 7, 12, 18, 25 and 90 days. Epileptic phenomena induced by a subcutaneous injection of a 100 mg/kg dose of metrazol (isolated myoclonic jerk, minimal metrazol seizures and major, generalized tonic-clonic metrazol seizures) were used as a model. ORG 6370 did not influence myoclonic jerks or minimal metrazol seizures in those age groups where they were regularly elicited. In 12-day-old rats pretreatment with ORG 6370 led to the appearance of minimal metrazol seizures, a phenomenon rarely seen under control conditions. Major seizures were suppressed only in adult rats with a 20 mg/kg dose; on the other hand, ORG 6370 exhibited a selective action against the tonic phase of major seizures at all stages of development. The profile of action of ORG 6370 is almost the same as that of phenytoin.
对一种新型抗癫痫药物ORG 6370(欧加农国际有限公司)的抗惊厥作用进行了研究,实验对象为217只7日龄、12日龄、18日龄、25日龄和90日龄的雄性白化大鼠。皮下注射100mg/kg剂量的戊四氮所诱发的癫痫现象(孤立性肌阵挛抽搐、轻度戊四氮惊厥和严重的全身性强直阵挛性戊四氮惊厥)被用作模型。ORG 6370对那些经常引发肌阵挛抽搐或轻度戊四氮惊厥的年龄组没有影响。在12日龄大鼠中,用ORG 6370预处理会导致轻度戊四氮惊厥的出现,这一现象在对照条件下很少见。仅在成年大鼠中,20mg/kg的剂量才能抑制严重惊厥;另一方面,ORG 6370在发育的各个阶段都对严重惊厥的强直期表现出选择性作用。ORG 6370的作用模式与苯妥英几乎相同。