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多巴胺“自身受体”:通过微离子电泳单细胞记录研究进行的药理学特性分析

Dopamine"autoreceptors": pharmacological characterization by microiontophoretic single cell recording studies.

作者信息

Aghajanian G K, Bunney B S

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1977 Mar;297(1):1-7. doi: 10.1007/BF00508803.

Abstract

The effects on the firing of single dopamine (DA) neurons in the substantia nigra (and adjacent ventral tegmental area) of a representative group of catecholamine agonists and antagonists were studied in rats using single cell recording and microiontophoretic techniques. Microiontophoretic application of DA or the DA agonist apomorphine depressed the firing of these cells; the DA antagonist trifluoperazine blocked this effect. However, the alpha-agonist clonidine had no depressant effect and the beta-agonist isoproteronol had only a weak depressant action on DA neurons. Furthermore, the alpha-antagonist piperoxane and the beta-antagonist sotolol were completely ineffective in blocking the depressant effects of DA. These results show that DA-sensitive receptors on the soma of DA neurons are pharmacologically distinct from alpha or beta adrenoreceptors. Because of their location and selective responsiveness to DA agonists, the catecholamine receptors on the soma of DA neurons appear best classified as DA "autoreceptors".

摘要

运用单细胞记录和微量离子电泳技术,在大鼠中研究了一组具有代表性的儿茶酚胺激动剂和拮抗剂对黑质(以及相邻的腹侧被盖区)中单个多巴胺(DA)神经元放电的影响。通过微量离子电泳施加DA或DA激动剂阿扑吗啡可抑制这些细胞的放电;DA拮抗剂三氟拉嗪可阻断此效应。然而,α激动剂可乐定无抑制作用,β激动剂异丙肾上腺素对DA神经元仅有微弱的抑制作用。此外,α拮抗剂哌罗克生和β拮抗剂索他洛尔在阻断DA的抑制作用方面完全无效。这些结果表明,DA神经元胞体上对DA敏感的受体在药理学上与α或β肾上腺素能受体不同。由于其位置以及对DA激动剂的选择性反应,DA神经元胞体上的儿茶酚胺受体似乎最好归类为DA“自身受体”。

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