Zabik J E, Levine R M, Maickel R P
Pharmacol Biochem Behav. 1978 Apr;8(4):429-35. doi: 10.1016/0091-3057(78)90081-3.
Administration of single IP doses of 1.0 or 4.0 mg/kg of d-amphetamine evoked an increase in mouse spontaneous motor activity (SMA); in contrast, 1.0 mg/kg of l-amphetamine had no significant effect, while 4.0 mg/kg caused a decreased SMA. Pretreatment with aMT or pargyline had little effect on the actions of the l-isomer, but reduced the magnitude and duration of the stimulatory effect of d-amphetamine. Pretreatment with p-chlorophenylalanine had little effect on the actions of d-amphetamine but completely abolished the depressant actions of the l-isomer. Reserpine pretreatment markedly reduced basal SMA levels; such pretreatment caused both d- and l-amphetamine to act as stimulants of SMA.
腹腔注射单剂量1.0或4.0毫克/千克的右旋苯丙胺可引起小鼠自发运动活动(SMA)增加;相比之下,1.0毫克/千克的左旋苯丙胺无显著影响,而4.0毫克/千克则导致SMA降低。用α-甲基酪氨酸(aMT)或帕吉林预处理对左旋异构体的作用影响不大,但可降低右旋苯丙胺刺激作用的强度和持续时间。用对氯苯丙氨酸预处理对右旋苯丙胺的作用影响不大,但完全消除了左旋异构体的抑制作用。利血平预处理显著降低基础SMA水平;这种预处理使右旋和左旋苯丙胺均表现为SMA的兴奋剂。