Moore K E
Biol Psychiatry. 1977 Jun;12(3):451-62.
The central stimulant actions of d-amphetamine are not altered in animals in which brain stores of catecholamines have been depleted with reserpine, but they are blocked by alpha-methyltyrosine, which inhibits catecholamine synthesis. The results of a variety of experiments suggest that the central actions of amphetamine result primarily from the ability of the drug to facilitate the release of newly synthesized dopamine from nerve terminals in the forebrain. The results of experiments in animals in which dopaminergic nerve terminals in various brain regions have been selectively destroyed by intracranial microinjection of 6-hydroxydopamine reveal that the locomotor stimulant actions of relatively low doses of amphetamine are dependent upon mesolimbic dopaminergic neurons, whereas the stereotyped behaviors induced by relatively larger doses of amphetamine are dependent upon nigrostriatal dopaminergic neurons. The central actions of amphetamine appear to be the primary result of interactions with dopamine neurons, but secondarily the drug also alters the dynamics of other putative neurotransmitters (e.g. acetylcholine, 5-hydroxytryptamine) in the brain.
在使用利血平使儿茶酚胺脑内储存耗竭的动物中,d-苯丙胺的中枢兴奋作用并未改变,但它们会被抑制儿茶酚胺合成的α-甲基酪氨酸所阻断。各种实验结果表明,苯丙胺的中枢作用主要源于该药物促进前脑神经末梢释放新合成多巴胺的能力。在通过颅内微量注射6-羟基多巴胺选择性破坏不同脑区多巴胺能神经末梢的动物实验中,结果显示相对低剂量苯丙胺的运动兴奋作用依赖于中脑边缘多巴胺能神经元,而相对高剂量苯丙胺诱导的刻板行为则依赖于黑质纹状体多巴胺能神经元。苯丙胺的中枢作用似乎主要是与多巴胺神经元相互作用的结果,但其次该药物也会改变脑内其他假定神经递质(如乙酰胆碱、5-羟色胺)的动态变化。