Rosecrans J A, Glennon R A
Department of Pharmacology, Medical College of Virginia, Virginia Commonwealth University, Richmond, 23298.
Pharmacol Biochem Behav. 1987 Sep;28(1):39-42. doi: 10.1016/0091-3057(87)90008-6.
The behaviorally disruptive effects of the optical isomers of 1-(3,4-methylenedioxyphenyl-2-aminopropane) (MDA) and its N-methyl derivative (MDMA) were evaluated in 27 mice trained to bar-press for a liquid food reinforcement. In addition, a second study was conducted in which mice were pretreated with either saline or the 5-HT-2 antagonist, pirenpirone, prior to the administration of either MDMA or MDA using the same behavioral procedure. The results indicated that the behaviorally disruptive effects produced only by R(-)-MDA, but not those of S(+)-MDA, R(-)-MDA, nor of S(+)-MDMA, were significantly attenuated by pirenpirone. These findings support previous research findings which indicate that this isomer may be producing its behaviorally disruptive effects via an action on 5-HT-2 receptors.
在27只经训练通过按压杠杆获取液体食物强化物的小鼠中,评估了1-(3,4-亚甲二氧基苯基)-2-氨基丙烷(MDA)及其N-甲基衍生物(MDMA)的旋光异构体对行为的干扰作用。此外,还进行了第二项研究,采用相同的行为程序,在给予MDMA或MDA之前,用生理盐水或5-HT-2拮抗剂匹仑哌隆对小鼠进行预处理。结果表明,仅R(-)-MDA产生的行为干扰作用,而不是S(+)-MDA、R(-)-MDMA或S(+)-MDMA的行为干扰作用,被匹仑哌隆显著减弱。这些发现支持了先前的研究结果,即该异构体可能通过作用于5-HT-2受体产生其行为干扰作用。