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中枢神经系统中对D1多巴胺受体刺激的功能性反应:抑制大鼠黑质中[3H] - 5-羟色胺的释放。

A functional response to D1 dopamine receptor stimulation in the central nervous system: inhibition of the release of [3H]-serotonin from the rat substantia nigra.

作者信息

Benkirane S, Arbilla S, Langer S Z

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1987 May;335(5):502-7. doi: 10.1007/BF00169115.

Abstract

The influence of dopamine receptor agonists on the calcium dependent electrically-evoked release of [3H]-serotonin was studied in the superfused rat substantia nigra. The electrically-evoked overflow of [3H]-serotonin was significantly inhibited by micromolar concentrations of exogenous dopamine and of the D1-selective dopamine receptor agonists, fenoldopam and SKF 38393. The inhibitory effects of dopamine and fenoldopam on [3H]-serotonin release were antagonized by the D1-selective dopamine receptor antagonist SCH 23390. S-sulpiride, an antagonist of D2 receptors failed to antagonize the inhibitory effects of dopamine on [3H]-serotonin release. Moreover, quinperol, the selective D2 receptor agonist did not modify the electrically evoked release of [3H]-serotonin. In the presence of nomifensine, SCH 23390 but not S-sulpiride enhanced in a concentration dependent manner the electrically-evoked release of [3H]-serotonin. Under similar experimental conditions, exposure to fenoldopam did not inhibit the electrically-evoked release of [3H]-serotonin from rat hippocampal or hypothalamic slices. These results indicate that, in rat substantia nigra, exogenous as well as endogenous dopamine causes inhibition of serotonin release by activation of dopamine receptors of the D1-subtype.

摘要

在灌流的大鼠黑质中研究了多巴胺受体激动剂对钙依赖性电诱发的[3H] - 5 - 羟色胺释放的影响。微摩尔浓度的外源性多巴胺以及D1选择性多巴胺受体激动剂非诺多泮和SKF 38393可显著抑制电诱发的[3H] - 5 - 羟色胺溢出。多巴胺和非诺多泮对[3H] - 5 - 羟色胺释放的抑制作用被D1选择性多巴胺受体拮抗剂SCH 23390拮抗。D2受体拮抗剂S - 舒必利未能拮抗多巴胺对[3H] - 5 - 羟色胺释放的抑制作用。此外,选择性D2受体激动剂喹吡罗未改变电诱发的[3H] - 5 - 羟色胺释放。在诺米芬辛存在的情况下,SCH 23390而非S - 舒必利以浓度依赖性方式增强电诱发的[3H] - 5 - 羟色胺释放。在类似的实验条件下,暴露于非诺多泮并未抑制大鼠海马或下丘脑切片中电诱发的[3H] - 5 - 羟色胺释放。这些结果表明,在大鼠黑质中,外源性和内源性多巴胺通过激活D1亚型多巴胺受体导致5 - 羟色胺释放受到抑制。

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