Schaefer G J, Michael R P
Neuropharmacology. 1984 Aug;23(8):909-14. doi: 10.1016/0028-3908(84)90004-2.
The locomotor activity of female rats was recorded during 10-min sessions in a circular open-field apparatus after the administration of vehicle or drug. Dose-response curves were obtained for seven neuroleptic drugs both alone (spontaneous activity) and in combination with 1.0 mg/kg of d-amphetamine. Haloperidol, pimozide, loxapine, thiothixene, molindone and chlorpromazine all produced graded decreases in spontaneous locomotor activity. Haloperidol, pimozide, loxapine, thiothixene and molindone also produced graded reversals of the hyperactivity produced by d-amphetamine, while chlorpromazine did not. Clozapine neither altered spontaneous activity nor reversed the hyperactivity produced by d-amphetamine. The data indicate that measures of locomotor activity provide important additional information about the actions of neuroleptics and do not necessarily mirror the actions of these drugs on other measures of performance such as lever-pressing for brain stimulation.
在给予赋形剂或药物后,在圆形旷场装置中对雌性大鼠进行10分钟的运动活动记录。获得了七种抗精神病药物单独使用(自发活动)以及与1.0mg/kg的d-苯丙胺联合使用时的剂量-反应曲线。氟哌啶醇、匹莫齐特、洛沙平、硫利达嗪、莫林酮和氯丙嗪均使自发运动活动产生分级下降。氟哌啶醇、匹莫齐特、洛沙平、硫利达嗪和莫林酮也使d-苯丙胺引起的多动产生分级逆转,而氯丙嗪则没有。氯氮平既不改变自发活动,也不逆转d-苯丙胺引起的多动。数据表明,运动活动测量为抗精神病药物的作用提供了重要的额外信息,且不一定反映这些药物对其他行为测量指标(如为脑刺激而按压杠杆)的作用。