Chermat R, Simon P, Boissier J R
Arzneimittelforschung. 1979;29(5):814-20.
2-Chloro-11-(piperazinyl)dibenz[b,f][1,4]-oxazepine (amoxapine) gives an unusual spectrum in psychopharmacological tests. Many of its effects are similar to those of neuroleptics: sedation, decrease in motor activity, catalepsy (which is, however, qualitatively different from that induced by classical neuroleptics), transitory suppression of avoidance reaction, antagonism of amphetamine induced toxicity in crowded mice and inhibition of stereotyped behavior induced by amphetamine in rats, and antagonism to various effects of apomorphine (stereotyped behaviour in rats, climbing behaviour, stereotyped behaviour and hypothermia in mice). At similar doses which produce the above mentioned effects, amoxapine also shows effects atypical for a neuroleptic, but which are relatively characteristic of antidepressants: antagonism of prochlorperazine-induced catalepsy in rats, inhibition of reserpine induced hypothermia in mice and enhancement of yohimbine toxicity in mice. The profile of this substance does not facilitate the anticipation of therapeutic effects in humans.
2-氯-11-(哌嗪基)二苯并[b,f][1,4] - 恶氮平(阿莫沙平)在精神药理学测试中呈现出不同寻常的谱图。它的许多作用与抗精神病药物相似:镇静、运动活性降低、僵住症(然而,其性质与经典抗精神病药物诱导的僵住症不同)、回避反应的短暂抑制、拥挤小鼠中苯丙胺诱导毒性的拮抗作用以及大鼠中苯丙胺诱导的刻板行为的抑制,以及对阿扑吗啡各种作用的拮抗作用(大鼠的刻板行为、小鼠的攀爬行为、刻板行为和体温过低)。在产生上述作用的相似剂量下,阿莫沙平还表现出抗精神病药物不典型但相对具有抗抑郁药特征的作用:拮抗大鼠中氯丙嗪诱导的僵住症、抑制小鼠中利血平诱导的体温过低以及增强小鼠中育亨宾的毒性。该物质的特性不利于预测其在人类中的治疗效果。