Chow H L, Beck C H
Eur J Pharmacol. 1984 Jul 13;102(2):297-304. doi: 10.1016/0014-2999(84)90261-9.
Following an initial rise in locomotor activity, apomorphine in large doses causes a concurrent rise in brain serotonin levels, locomotor akinesia, and stereotypic gnawing. However, reports to date have failed to observe any effect of pretreatment with serotonin depletors parachlorophenylalanine (pCPA) or parachloroamphetamine (pCA) on apomorphine-induced stereotypy. In the present study the effects of pCPA (250 or 400 mg/kg i.p., 3 days) and pCA (6.4 or 10.4 mg/kg i.p., 3 days) pretreatment on apomorphine-induced (5.0 mg/kg s.c., 5 min) behavior of male rats in the open-field were compared. For half of the trials in the 78 min session, the rats were alone and for half of the trials they were paired with an untreated male rat. pCA pretreatment increased the frequency of line-crossing and of jumping, whereas pCPA pretreatment increased the duration of bouts of locomotion and gnawing. These behavioral differences may be related to the interaction of pCA and pCPA with dopaminergic subsystems in the brain.
在最初的运动活动增加之后,大剂量的阿扑吗啡会导致脑血清素水平同时升高、运动不能以及刻板啃咬行为。然而,迄今为止的报告未能观察到用血清素耗竭剂对氯苯丙氨酸(pCPA)或对氯苯丙胺(pCA)进行预处理对阿扑吗啡诱导的刻板行为有任何影响。在本研究中,比较了pCPA(250或400毫克/千克腹腔注射,3天)和pCA(6.4或10.4毫克/千克腹腔注射,3天)预处理对阿扑吗啡诱导的(5.0毫克/千克皮下注射,5分钟)雄性大鼠在旷场中的行为的影响。在78分钟的实验过程中,一半的实验大鼠单独放置,另一半与未处理的雄性大鼠配对。pCA预处理增加了穿越线条和跳跃的频率,而pCPA预处理增加了运动和啃咬发作的持续时间。这些行为差异可能与pCA和pCPA与脑中多巴胺能子系统的相互作用有关。