Ashton C, Anlezark G, Meldrum B
Eur J Pharmacol. 1976 Oct;39(2):399-401. doi: 10.1016/0014-2999(76)90151-5.
In baboons, Papio papio, spontaneously showing photosensitive epilepsy, myoclonic responses to intermittent photic stimulation were reduced or abolished for up to four hours by (+/-)-N-n-propylnorapomorphine (NPA) 0.05-0.2 mg/kg body weight, given i.v. In animals pretreated with allyglycine, 200 mg/kg, a transient abolition of myoclonic responses followed NPA, 0.2 mg/kg. In DBA/2 mice, seizures following auditory stimulation were attenuated or abolished by NPA 0.025-0.1 mg/kg given intraperitoneally (ED50 for abolition of clonic phase = 0.032 mg/kg). The ED50 for pentylenetetrazol seizures in MF 1 mice was not altered by NPA 0.25 mg/kg.
在自然发生光敏性癫痫的豚尾狒狒(Papio papio)中,静脉注射体重0.05 - 0.2 mg/kg的(±)-N-正丙基去甲阿朴吗啡(NPA)可使对间歇性光刺激的肌阵挛反应减少或消失长达4小时。在用200 mg/kg的烯丙甘氨酸预处理的动物中,注射0.2 mg/kg的NPA后,肌阵挛反应会短暂消失。在DBA/2小鼠中,腹腔注射0.025 - 0.1 mg/kg的NPA可减轻或消除听觉刺激后的癫痫发作(消除阵挛期的半数有效量 = 0.032 mg/kg)。0.25 mg/kg的NPA不会改变MF 1小鼠戊四氮癫痫发作的半数有效量。