Furmidge L, Tong Z Y, Petry N, Clark D
Department of Psychology, University of Reading, United Kingdom.
J Neural Transm Gen Sect. 1991;86(1):61-70. doi: 10.1007/BF01250376.
The ability of low doses of the dopamine (DA) agonists quinpirole and (+)-3-PPP to reduce the discriminative stimulus properties and locomotor hyperactivity produced by d-amphetamine (0.5 mg/kg) was assessed in two groups of rats. Quinpirole (0.0125-0.05 mg/kg) and (+)-3-PPP (1.0-2.0 mg/kg) completely antagonized d-amphetamine-induced locomotor hyperactivity. In contrast, only single doses of quinpirole (0.025 mg/kg) and (+)-3-PPP (2.0 mg/kg) were effective in the drug discrimination paradigm; the antagonisms were small (18-47%), but significant. The inhibitory effects of quinpirole and (+)-3-PPP in these behavioural models are probably due to their ability to selectively stimulate DA autoreceptors in the nucleus accumbens and reduce the increase in DA release produced by d-amphetamine. It is suggested that the much weaker effects of the drugs in the discrimination paradigm are due to changes produced by the long-term periodic administration of d-amphetamine to these animals, such as a down-regulation in the sensitivity of DA autoreceptors.
在两组大鼠中评估了低剂量多巴胺(DA)激动剂喹吡罗和(+)-3-PPP降低由d-苯丙胺(0.5mg/kg)产生的辨别刺激特性和运动性多动的能力。喹吡罗(0.0125 - 0.05mg/kg)和(+)-3-PPP(1.0 - 2.0mg/kg)完全拮抗d-苯丙胺诱导的运动性多动。相比之下,在药物辨别范式中只有单剂量的喹吡罗(0.025mg/kg)和(+)-3-PPP(2.0mg/kg)有效;拮抗作用较小(18 - 47%),但具有显著性。喹吡罗和(+)-3-PPP在这些行为模型中的抑制作用可能是由于它们能够选择性刺激伏隔核中的DA自身受体并减少d-苯丙胺引起的DA释放增加。提示药物在辨别范式中作用较弱是由于对这些动物长期周期性给予d-苯丙胺所产生的变化,如DA自身受体敏感性的下调。