Song H K, Hamada K, Yagi K, Seino M
National Epilepsy Center, Shizuoka Hospital, Japan.
Epilepsy Res. 1997 May;27(2):81-7. doi: 10.1016/s0920-1211(96)01012-1.
In this study, we assessed the anti-convulsive effects of sulthiame (SUL) in amygdaloid (AM) kindled rats. Electrodes were implanted into the left AM of adult male Wistar rats. The animals were kindled at the after-discharge (AD) threshold. Upon completion of kindling, a generalized seizure triggering threshold was determined. The drugs were administered intraperitoneally in rats which reproducibly exhibited generalized convulsions at the near-threshold stimulation. Single administration of SUL (25-200 mg; n = 7-9) reduced the forelimb clonus (FCL) duration, but only the highest dose significantly regressed the secondarily generalized convulsion. During repeated administration of SUL, 50 mg/kg for 8 days, FCL duration was significantly alleviated until the fifth treatment day. With the dose of 200 mg/kg, significant suppression of secondary generalization was noted only until the second test day. On the other hand, significant reductions of FCL and AD duration were preserved afterwards. The anti-convulsive effects of SUL indicated in this study were not comparable to those of other standard anti-epileptic drugs reported from our laboratory.
在本研究中,我们评估了舒噻美(SUL)对杏仁核(AM)点燃大鼠的抗惊厥作用。将电极植入成年雄性Wistar大鼠的左侧杏仁核。在放电后(AD)阈值处对动物进行点燃。点燃完成后,确定全身性癫痫发作触发阈值。在接近阈值刺激时可重复性地表现出全身性惊厥的大鼠中腹腔注射药物。单次给予SUL(25 - 200毫克;n = 7 - 9)可缩短前肢阵挛(FCL)持续时间,但只有最高剂量能显著减轻继发性全身性惊厥。在重复给予SUL(50毫克/千克,持续8天)期间,FCL持续时间在第五次治疗日之前显著减轻。使用200毫克/千克的剂量时,仅在第二次测试日之前观察到对继发性泛化的显著抑制。另一方面,之后FCL和AD持续时间仍显著缩短。本研究中显示的SUL的抗惊厥作用与我们实验室报道的其他标准抗癫痫药物的作用不可比。