Functional classification of different dopamine receptors.

U Ungerstedt, M Herrera-Marschitz, L Ståhle, U Tossman, T Zetterström
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引用次数: 11

Abstract

A series of experiments is described in which behavioral models and intracerebral dialysis were used to study neurotransmitter release and which illustrate the functional properties of different dopamine receptors. Evidence is presented for the existence of postsynaptic D-1 dopamine receptors, which are preferentially stimulated by apomorphine and inhibited by SCH 23390, and postsynaptic D-2 receptors, which are preferentially stimulated by pergolide and inhibited by sulpiride. On the basis of results obtained following systemic and local treatment with picrotoxin it seems probable that D-2 receptors are located on GABA interneurons in the striatum. Furthermore, lesion studies indicate that the D-1 and D-2 receptors are related to different neuronal pathways. In contrast to postsynaptic dopamine receptors, presynaptic autoreceptors, as studied by recording the decrease in exploratory behavior and dopamine release, seem not to differ in their response to apomorphine and pergolide. Sulpiride selectively inhibits dopamine autoreceptors and is equally potent in inhibiting apomorphine and pergolide autoreceptor-dependent responses. In summary, the data strongly support the existence of functionally important D-1 and D-2 receptors.

不同多巴胺受体的功能分类。
本文描述了一系列的实验,其中使用行为模型和脑内透析来研究神经递质释放,并说明了不同多巴胺受体的功能特性。有证据表明,突触后的D-1多巴胺受体优先受到阿波啡的刺激,并被SCH 23390抑制;突触后的D-2受体优先受到培高利特的刺激,并被舒必利抑制。根据在全身和局部使用微毒素治疗后获得的结果,D-2受体可能位于纹状体的GABA中间神经元上。此外,病变研究表明,D-1和D-2受体与不同的神经元通路有关。与突触后多巴胺受体相比,通过记录探索行为和多巴胺释放的减少,突触前自受体对阿波啡和培高利特的反应似乎没有区别。舒必利选择性地抑制多巴胺自身受体,同样有效地抑制阿波啡和培高利特自身受体依赖反应。总之,这些数据有力地支持了D-1和D-2受体的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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