Glennon R A, Little P J, Rosecrans J A, Yousif M
Pharmacol Biochem Behav. 1987 Feb;26(2):425-6. doi: 10.1016/0091-3057(87)90141-9.
Eleven mice were trained to respond under an FR 20 schedule of reinforcement and, after learning the schedule, were administered doses of saline and the following phenylisopropylamines: (+/-)-MDMA, S(+)-MDMA, R(-)-MDMA and (+)-amphetamine. Each of the phenylisopropylamines decreased rates of operant responding in a dose-dependent manner. S(+)-MDMA (ED50 = 3.1 mg/kg) was nearly equipotent with racemic MDMA and four times more potent than R(-)-MDMA (ED50 = 4.1 and 11.6 mg/kg, respectively), but less potent than (+)-amphetamine (ED50 = 0.74 mg/kg). The present study constitutes the first enantiomeric behavioral-potency comparison for the optical isomers of MDMA.
11只小鼠接受训练,在固定比率为20的强化程序下做出反应。在学会该程序后,给它们注射生理盐水以及以下苯基异丙胺:(±)-摇头丸、S(+)-摇头丸、R(-)-摇头丸和(+)-苯丙胺。每种苯基异丙胺都以剂量依赖的方式降低了操作性反应的速率。S(+)-摇头丸(半数有效剂量[ED50]=3.1毫克/千克)与消旋摇头丸的效力几乎相当,比R(-)-摇头丸(ED50分别为4.1和11.6毫克/千克)强四倍,但比(+)-苯丙胺(ED50=0.74毫克/千克)效力弱。本研究是对摇头丸光学异构体进行的首次对映体行为效力比较。