Huang D, Wilson M C
Pharmacol Biochem Behav. 1986 Feb;24(2):205-10. doi: 10.1016/0091-3057(86)90339-4.
The discriminative stimulus properties of dl-cathinone (dl-CAT), d-amphetamine (d-A), and cocaine (COC) were compared and effects of haloperidol pretreatment on these properties were studied in rats. The ED50's of each drug were also determined. Stimulus generalization (i.e., greater than 75% of responses occurring on the drug lever) occurred with each of the three training drugs to all three test drugs. The degree of generalization was less between d-amphetamine and dl-cathinone than between d-amphetamine and cocaine or between cocaine and dl-cathinone. No significant differences were observed among the ED50's of each test drug obtained in all three training groups. Pretreatment with haloperidol failed to alter the stimulus properties of dl-cathinone. Haloperidol administration did partially antagonize the stimulus complex induced by d-amphetamine and cocaine. It is concluded that all three agents share somewhat similar but not identical, stimulus properties. The stimulus properties of the training dose of d-amphetamine may be somewhat different from those of dl-cathinone and may be more dependent on functional dopaminergic pathways.
比较了消旋去甲伪麻黄碱(dl-CAT)、右旋苯丙胺(d-A)和可卡因(COC)的辨别性刺激特性,并研究了氟哌啶醇预处理对大鼠这些特性的影响。还测定了每种药物的半数有效剂量(ED50)。三种训练药物中的每一种对所有三种测试药物都出现了刺激泛化(即,75%以上的反应发生在药物杆上)。右旋苯丙胺和消旋去甲伪麻黄碱之间的泛化程度低于右旋苯丙胺和可卡因之间或可卡因和消旋去甲伪麻黄碱之间。在所有三个训练组中获得的每种测试药物的ED50之间未观察到显著差异。氟哌啶醇预处理未能改变消旋去甲伪麻黄碱的刺激特性。给予氟哌啶醇确实部分拮抗了由右旋苯丙胺和可卡因诱导的刺激复合体。得出的结论是,所有三种药物具有一些相似但不完全相同的刺激特性。右旋苯丙胺训练剂量的刺激特性可能与消旋去甲伪麻黄碱的刺激特性有些不同,并且可能更依赖于功能性多巴胺能通路。