Alves C R, Silva M T
Department of Experimental Psychology, Institute of Psychology, University of São Paulo, Avenida Professor Mello Moraes 1721, 05508-900, SP, São Paulo, Brazil.
Pharmacol Biochem Behav. 2001 Mar;68(3):503-6. doi: 10.1016/s0091-3057(01)00475-0.
The action of the atypical antipsychotic risperidone on latent inhibition (LI), an animal model of schizophrenia, was investigated. The parameters of the procedure were set at values insufficient to generate LI in control rats. On the first day, rats administered 0.5, 1.0, or 2.0 mg/kg ip risperidone or vehicle were preexposed (PE) to 10 tone presentations. On the second day, they were again injected with drug or vehicle and then submitted to two conditioned stimulus (CS; tone)-unconditioned stimulus (US; shock) pairings. On the third day, suppression of their drinking response under the CS was measured. Nonpreexposed (NPE) animals were submitted to the same procedure except for the tone preexposure. On the suppression test, LI was not observed in control rats as well as in animals given 0.5 mg/kg risperidone. Animals given 1.0 and 2.0 mg risperidone, however, displayed an LI effect. The facilitation of LI by risperidone gives additional support to the LI paradigm as an animal model of schizophrenia.
研究了非典型抗精神病药物利培酮对潜伏抑制(LI)这一精神分裂症动物模型的作用。实验程序的参数设定为在对照大鼠中不足以产生潜伏抑制的值。第一天,腹腔注射0.5、1.0或2.0mg/kg利培酮或赋形剂的大鼠接受10次纯音刺激的预暴露(PE)。第二天,再次给它们注射药物或赋形剂,然后进行两次条件刺激(CS;纯音)-非条件刺激(US;电击)配对。第三天,测量它们在条件刺激下饮水反应的抑制情况。除了没有纯音预暴露外,未预暴露(NPE)的动物接受相同的程序。在抑制试验中,对照大鼠以及给予0.5mg/kg利培酮的动物中未观察到潜伏抑制。然而,给予1.0和2.0mg利培酮的动物表现出潜伏抑制效应。利培酮对潜伏抑制的促进作用为潜伏抑制范式作为精神分裂症动物模型提供了额外的支持。