Stavchansky S, Riffee W, Geary R
Res Commun Chem Pathol Pharmacol. 1985 May;48(2):189-202.
Comparative studies were pursued to investigate the locomotor activity induced by phencyclidine hydrochloride in CD-1 male mice. Horizontal, vertical, and rotational activity counts were quantitated using an infrared beam animal activity monitor. Five doses (1.5, 2.5, 3.5, 5.0, and 10.0 mg/kg, i.p.) of phencyclidine were compared. At the 1.5 mg/kg dose, no locomotor activity changes were observed when compared to a saline control group. Increased activity was observed at the 2.5, 3.5, and 5.0 mg/kg doses. Decreased activity was observed at the 10.0 mg/kg dose when compared to the 5.0 mg/kg dose possibly due to ataxia. In addition, the locomotor activity produced by acute d-amphetamine and acute phencyclidine was compared at doses of 2.5 mg/kg and 5.0 mg/kg respectively. The overall locomotor activity levels produced by acute d-amphetamine and phencyclidine were not significantly different at p less than 0.05. The time to peak activities and peak level activities were also similar and occurred at 20-25 minutes and 1100-1300 inches respectively after i.p. administration. Administration of apomorphine after phencyclidine did not change overall locomotor activity. The data implies that phencyclidine may act primarily as a dopamine reuptake inhibitor rather than a dopamine release stimulator. Phencyclidine also affects other activity (unlike amphetamine) as seen by the severe depression of vertical activity.
开展了比较研究,以调查盐酸苯环己哌啶对CD-1雄性小鼠运动活性的影响。使用红外光束动物活动监测仪对水平、垂直和旋转活动计数进行定量分析。比较了苯环己哌啶的五个剂量(1.5、2.5、3.5、5.0和10.0毫克/千克,腹腔注射)。在1.5毫克/千克剂量下,与生理盐水对照组相比,未观察到运动活性变化。在2.5、3.5和5.0毫克/千克剂量下观察到活性增加。与5.0毫克/千克剂量相比,在10.0毫克/千克剂量下观察到活性降低,这可能是由于共济失调所致。此外,分别比较了急性右旋苯丙胺和急性苯环己哌啶在2.5毫克/千克和5.0毫克/千克剂量下产生的运动活性。急性右旋苯丙胺和苯环己哌啶产生的总体运动活性水平在p小于0.05时无显著差异。达到峰值活性的时间和峰值活性水平也相似,腹腔注射后分别在20 - 25分钟和1100 - 1300英寸时出现。苯环己哌啶给药后注射阿扑吗啡并未改变总体运动活性。数据表明,苯环己哌啶可能主要作为多巴胺再摄取抑制剂而非多巴胺释放刺激剂起作用。如垂直活性严重降低所示,苯环己哌啶还会影响其他活性(与苯丙胺不同)。