Department of Psychology, Institute of Psychiatry, De Crespigny Park, Denmark Hill, London SE5 8AF, UK.
J Psychopharmacol. 1993 Jan;7(1 Suppl):63-71. doi: 10.1177/026988119300700110.
When animals are exposed to a stimulus that has no consequences they are subsequently impaired in learning that this stimulus predicts an important event, such as footshock. This retarding effect of stimulus pre-exposure is called latent inhibition (LI) and is reliably disrupted by amphetamine, antipsychotics having an opposite effect. The present experiments investigated whether agents which affect serotonergic transmission also attenuate LI, using a conditioned suppression of drinking procedure. The results showed that the 5-HT(2) antagonist ritanserin (2.0 mg/kg), and the 5-HT(1b) agonist RU 24969 (0.5 and 10.0 mg/kg) attenuated LI by increasing learning in pre-exposed animals, whilst the effects of the 5-HT(1a) agonist 8-OH-DPAT (0.38 mg/kg), though in a similar direction, were not significant. These experiments provide partial support for the involvement of serotonin in LI. Since amphetamine-induced attenuation of LI has been proposed as a model for the attentional deficits found in acute schizophrenia, these results are discussed in terms of the possible involvement of reduced serotonergic function in schizophrenic attentional disorder.
当动物暴露于没有后果的刺激下时,它们随后在学习中受到损害,即这种刺激预测了一个重要事件,例如足部电击。这种刺激前暴露的延迟效应称为潜伏抑制(LI),并且被安非他命可靠地破坏,具有相反作用的抗精神病药也是如此。本实验研究了影响 5-羟色胺能传递的药物是否也会减弱 LI,使用条件抑制饮水程序。结果表明,5-HT2 拮抗剂利坦色林(2.0mg/kg)和 5-HT1b 激动剂 RU 24969(0.5 和 10.0mg/kg)通过增加预先暴露动物的学习来减弱 LI,而 5-HT1a 激动剂 8-OH-DPAT(0.38mg/kg)的作用虽然方向相似,但并不显著。这些实验为 5-羟色胺参与 LI 提供了部分支持。由于安非他命诱导的 LI 减弱已被提议作为急性精神分裂症中发现的注意力缺陷的模型,因此根据 5-羟色胺能功能降低在精神分裂症注意力障碍中的可能参与,对这些结果进行了讨论。