Zharkovskiĭ A M, Klassen N E, Zharkovskiĭ T A
Biull Eksp Biol Med. 1985 Jun;99(6):700-2.
It has been shown in experiments on mice and rats that unlike haloperidol and sulpiride, carbidine does not influence the intensity and even increases the duration of apomorphine stereotypy. However, similarly to haloperidol carbidine decreases head twitches in mice, induced by administration of 5-hydroxytryptophan. In radioligand-binding experiments in vitro and in vivo carbidine displaced 3H-spiperone but in the brain cortex without having any effect on the binding in the striatum. Carbidine did not affect the dopamine-sensitive adenylate cyclase in rat striatum. Based on these data it is suggested that in contrast to haloperidol and sulpiride, carbidine selectively inhibits serotonin receptors of the brain.
在对小鼠和大鼠的实验中已表明,与氟哌啶醇和舒必利不同,卡比定不影响阿扑吗啡刻板行为的强度,甚至会延长其持续时间。然而,与氟哌啶醇类似,卡比定可减少由5-羟色氨酸给药诱导的小鼠头部抽搐。在体外和体内的放射性配体结合实验中,卡比定可取代3H-螺哌隆,但在大脑皮层中起作用,而对纹状体中的结合没有任何影响。卡比定不影响大鼠纹状体中对多巴胺敏感的腺苷酸环化酶。基于这些数据,有人提出,与氟哌啶醇和舒必利相反,卡比定可选择性抑制大脑的5-羟色胺受体。