Carter C J, Pycock C J
Pharmacol Biochem Behav. 1979 Apr;10(4):475-80. doi: 10.1016/0091-3057(79)90220-x.
Apomorphine (0.12--2 mg/kg, SC) and d-amphetamine (1--8 mg/kg, IP) were each able, at certain doses, to potentiate the cataleptic state produced by the neuroleptic agent, haloperidol (1 mg/kg, IP). In subsequent biochemical experiments, in which the effects of combinations of apomorphine or d-amphetamine and haloperidol on brain monoamine levels were studied, this behavioural observation was seen to be related to an enhanced utilisation of 5-hydroxytryptamine (5-HT) in certain brain regions. The results suggest not only the possible involvement of 5-HT in the production of catalepsy, but also that the effects of these 'classical' dopamine agonists on other central transmitter systems should be considered when interpreting their various behavioural responses.
阿扑吗啡(0.12 - 2毫克/千克,皮下注射)和右旋苯丙胺(1 - 8毫克/千克,腹腔注射)在某些剂量下,均能够增强由抗精神病药物氟哌啶醇(1毫克/千克,腹腔注射)所产生的僵住状态。在随后的生化实验中,研究了阿扑吗啡或右旋苯丙胺与氟哌啶醇联合使用对脑单胺水平的影响,发现这种行为学观察结果与某些脑区中5-羟色胺(5-HT)利用率的提高有关。结果表明,5-HT不仅可能参与僵住症的产生,而且在解释这些“经典”多巴胺激动剂的各种行为反应时,应考虑它们对其他中枢递质系统的影响。