Sanger D J, Zivkovic B
Psychopharmacology (Berl). 1986;89(3):317-22. doi: 10.1007/BF00174367.
Zolpidem is a non-benzodiazepine hypnotic drug which displaces benzodiazepines from their binding sites in different brain structures. Previous work has demonstrated several differences between zolpidem and benzodiazepines, including differences between the stimulus properties of zolpidem and chlordiazepoxide. In the present study the discriminative stimulus properties of zolpidem were analysed by training rats to discriminate between this drug and saline. It was found that stimulus control developed readily with 2 mg/kg but not with 1 mg/kg zolpidem. The effect was dose-related, had a short duration of action and was antagonised by Ro 15-1788. Furthermore, stimulus control produced by zolpidem was associated with marked reductions in rates of responding. Injections of chlordiazepoxide, triazolam, lorazepam, zopiclone, CL 218,872 and pentobarbital produced dose-related responding on the zolpidem-associated lever but haloperidol did not. However, in general, the doses of those drugs which produced drug-lever responding also reduced response rates. It is possible that the above mentioned differences between the discriminative stimulus produced by zolpidem in rats and those produced by other sedatives may be due to a selective action of zolpidem on a sub-type of benzodiazepine binding site.
唑吡坦是一种非苯二氮䓬类催眠药物,它能将苯二氮䓬类药物从不同脑结构中的结合位点上置换出来。先前的研究已经证明了唑吡坦和苯二氮䓬类药物之间的一些差异,包括唑吡坦和氯氮䓬的刺激特性之间的差异。在本研究中,通过训练大鼠区分这种药物和生理盐水来分析唑吡坦的辨别刺激特性。发现2mg/kg的唑吡坦能很容易地建立刺激控制,而1mg/kg的唑吡坦则不能。这种效应与剂量相关,作用持续时间短,并且被Ro 15-1788拮抗。此外,唑吡坦产生的刺激控制与反应率的显著降低有关。注射氯氮䓬、三唑仑、劳拉西泮、佐匹克隆、CL 218,872和戊巴比妥在与唑吡坦相关的杠杆上产生剂量相关的反应,但氟哌啶醇则没有。然而,一般来说,那些产生药物杠杆反应的药物剂量也会降低反应率。大鼠中唑吡坦产生的辨别刺激与其他镇静剂产生的辨别刺激之间的上述差异可能是由于唑吡坦对苯二氮䓬结合位点亚型的选择性作用。