Dunn L A, Atwater G E, Kilts C D
Department of Psychiatry, Duke University Medical Center, Durham, NC 27710.
Psychopharmacology (Berl). 1993;112(2-3):315-23. doi: 10.1007/BF02244927.
Latent inhibition (LI) of a conditioned emotional response (CER) has been proposed as a quantitative measure of selective attention. We have assessed the parallels of the pharmacology of LI in rats with the clinical pharmacology of schizophrenia. Drug and vehicle treated rats were divided into groups and preexposed 20 times to cage illumination as a CS, or not preexposed. All groups were conditioned with 2 CS-footshock pairings. The following day CER, as measured by interruption of drinking in response to CS presentation, was recorded. LI was observed as a decreased CER in preexposed relative to non-preexposed animals. LI was enhanced by haloperidol 0.3 mg/kg after 7 or 14 daily treatments, but not after a single acute dose. Haloperidol doses of 0.3 and 0.03 mg/kg enhanced LI, while doses of 0.003 and 3.0 mg/kg had no effect. Haloperidol enhancement of LI was unaffected by the coadministration of the anticholinergic agent trihexyphenidyl. Enhancement of LI is exhibited by the antipsychotic drugs fluphenazine, chlorpromazine, thiothixene, thioridazine, mesoridazine, and metoclopramide but not clozapine. The non-antipsychotic drugs pentobarbital, imipramine, chlordiazepoxide, trihexyphenidyl, and promethazine failed to enhance LI. LI exhibits striking parallels to the clinical pharmacology of schizophrenia.
条件性情绪反应(CER)的潜伏抑制(LI)已被提议作为选择性注意的一种定量测量方法。我们评估了大鼠LI的药理学与精神分裂症临床药理学之间的相似性。将给予药物和赋形剂的大鼠分组,一组预先20次暴露于笼内光照作为条件刺激(CS),另一组不进行预先暴露。所有组均接受2次CS-足部电击配对。次日,记录通过对CS呈现做出反应时饮水中断来测量的CER。观察到LI表现为预先暴露的动物相对于未预先暴露的动物CER降低。在每日给药7次或14次后,0.3mg/kg的氟哌啶醇增强了LI,但单次急性给药后则无此效果。0.3mg/kg和0.03mg/kg的氟哌啶醇剂量增强了LI,而0.003mg/kg和3.0mg/kg的剂量则无作用。氟哌啶醇对LI的增强作用不受抗胆碱能药物三己芬迪的共同给药影响。抗精神病药物氟奋乃静、氯丙嗪、硫利达嗪、甲硫达嗪、美索达嗪和甲氧氯普胺表现出对LI的增强作用,但氯氮平没有。非抗精神病药物戊巴比妥、丙咪嗪、氯氮卓、三己芬迪和异丙嗪未能增强LI。LI与精神分裂症的临床药理学表现出显著的相似性。