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多巴胺能神经元对一种非苯丙胺类中枢神经系统兴奋剂的反应。

Dopaminergic neuronal responses to a non-amphetamine CNS stimulant.

作者信息

German D C, Harden H, Sanghera M K, Mann D, Kiser R S, Miller H H, Shore P A

出版信息

J Neural Transm. 1979;44(1-2):39-49. doi: 10.1007/BF01252700.

Abstract

The present study compares the effects of d-amphetamine (d-AMP) and the potent non-amphetamine CNS stimulant, amfonelic acid (AFA), on the firing rate of single midbrain dopaminergic (DA) neurons and on neostriatal DA metabolism (dihydroxyphenylacetic acid--DOPAC). The results indicate that AFA, like d-AMP, reduces the firing rate of DA neurons, although unlike d-AMP, AFA does not cause a decrease in neostriatal DOPAC content and, in fact, enhances that produced by haloperidol (HALO). The AFA-induced decrease in firing rate, like d-AMP, is reversed by the DA receptor blocker HALO, but again unlike d-AMP, the decrease in firing rate is not prevented by catecholamine synthesis inhibition with alpha-methyl-para-tyrosine. Thus, both amphetamine and amfonelic acid have identical electrophysiological effects on DA neurons but act by different mechanisms.

摘要

本研究比较了右旋苯丙胺(d-AMP)和强效非苯丙胺类中枢神经系统兴奋剂安福芬酸(AFA)对单个中脑多巴胺能(DA)神经元放电率以及对新纹状体DA代谢(二羟基苯乙酸——DOPAC)的影响。结果表明,AFA与d-AMP一样,会降低DA神经元的放电率,不过与d-AMP不同的是,AFA不会导致新纹状体DOPAC含量下降,实际上,它还会增强氟哌啶醇(HALO)所产生的DOPAC含量。AFA引起的放电率下降,与d-AMP一样,会被DA受体阻断剂HALO逆转,但同样与d-AMP不同的是,用α-甲基-对-酪氨酸抑制儿茶酚胺合成并不能阻止放电率的下降。因此,苯丙胺和安福芬酸对DA神经元具有相同的电生理效应,但作用机制不同。

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