Elchisak M A, Murrin L C, Roth R H, Maas J W
Psychopharmacol Commun. 1976;2(5-6):411-20.
Stimulation of the nigro-neostriatal dopamine pathway results in an accumulation of both free and conjugated dihydroxy-phenylacetic acid (DOPAC) in the rat neostriatum. Drugs which have previously been shown to alter impulse flow in central dopaminergic neurons also produce predictable changes in the levels of both free and conjugated DOPAC in both the neostriatum and, in most cases, in the frontal cortex. Drugs such as the antipsychotics which increase impulse flow in the nigro-neostriatal dopamine neurons increase both free and conjugated DOPAC levels in both the neostriatum and frontal cortex. Drugs which reduce impulse flow, such as d-amphetamine and apomorphine, cause a reduction in free DOPAC in both the neostriatum and frontal cortex but reduce DOPAC conjugate only in the neostriatum. Pargyline, a monoamine oxidase inhibitor, causes an extensive depletion of free and conjugated DOPAC in both the striatum and frontal cortex, indicating that these metabolites are rapidly cleared from both of these brain areas.
对黑质 - 新纹状体多巴胺通路的刺激会导致大鼠新纹状体内游离和结合型二羟基苯乙酸(DOPAC)的积累。先前已证明能改变中枢多巴胺能神经元冲动发放的药物,也会使新纹状体以及在大多数情况下额叶皮质中的游离和结合型DOPAC水平产生可预测的变化。诸如抗精神病药物等能增加黑质 - 新纹状体多巴胺神经元冲动发放的药物,会使新纹状体和额叶皮质中的游离和结合型DOPAC水平均升高。能减少冲动发放的药物,如d - 苯丙胺和阿扑吗啡,会使新纹状体和额叶皮质中的游离DOPAC减少,但仅使新纹状体中的DOPAC结合物减少。单胺氧化酶抑制剂帕吉林会导致纹状体和额叶皮质中游离和结合型DOPAC大量耗竭,这表明这些代谢产物会从这两个脑区迅速清除。