Cheal M
Psychopharmacology (Berl). 1984;84(2):268-73. doi: 10.1007/BF00427457.
Haloperidol (0, 0.1, 0.3, or 1.0 mg/kg), the typical butyrophenone neuroleptic, decreased investigation of novel objects by gerbils following systemic injections. When given prior to apomorphine (1 or 3 mg/kg), haloperidol blocked apomorphine-induced disruption of selective attention in a dose-dependent manner. Thus, haloperidol acts like pimozide in this paradigm. In contrast, clozapine (0, 0.03, 0.1, 0.3, 1.0, or 3.0 mg/kg), the atypical dibenzodiazepine neuroleptic, increased frequency of investigation both soon after injection and 24h later, suggesting interference with maintenance of attention. When given with apomorphine (1.0 mg/kg), clozapine did not block apomorphine effects on selective attention. The results are related to differential effects of these neuroleptics on other behaviors and to their individual pharmacological profiles.
典型的丁酰苯类抗精神病药物氟哌啶醇(0、0.1、0.3或1.0毫克/千克)经全身注射后,会减少沙鼠对新物体的探究行为。在给予阿扑吗啡(1或3毫克/千克)之前注射氟哌啶醇,它会以剂量依赖的方式阻断阿扑吗啡诱导的选择性注意力破坏。因此,在这个实验范式中,氟哌啶醇的作用与匹莫齐特相似。相比之下,非典型的二苯并二氮䓬类抗精神病药物氯氮平(0、0.03、0.1、0.3、1.0或3.0毫克/千克),在注射后不久及24小时后都会增加探究频率,这表明其对注意力维持存在干扰。当与阿扑吗啡(1.0毫克/千克)一起给予时,氯氮平不会阻断阿扑吗啡对选择性注意力的影响。这些结果与这些抗精神病药物对其他行为的不同作用及其各自的药理学特征有关。