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采用脑透析法研究局部应用 D-1 和 D-2 受体激动剂及拮抗剂的作用。

Effects of locally applied D-1 and D-2 receptor agonists and antagonists studied with brain dialysis.

作者信息

Imperato A, Di Chiara G

机构信息

Institute of Experimental Pharmacology and Toxicology, University of Cagliari, Italy.

出版信息

Eur J Pharmacol. 1988 Nov 8;156(3):385-93. doi: 10.1016/0014-2999(88)90284-1.

Abstract

The effect on dopamine (DA) release of D-1 and D-2 receptor agonists and antagonists applied locally in the caudate through a trans-striatal dialysis probe was studied in freely moving rats. D-2 agonists (LY 171555 and BHT 920) reduced DA release in a concentration-dependent manner. The same local application of haloperidol abolished the effect of 10 microM LY 171555 and BHT 920. A specific D-1 agonist, the catechol benzazepine SKF 38393, reduced DA release and this effect was not modified by systemic or local administration of the D-1 antagonist, SCH 23390, nor by the D-2 antagonist, haloperidol. In contrast, the non-catechol D-1 agonist, CY 208243, failed to modify DA release. Local application of the D-1 antagonist, SCH 23390, or of the D-2 antagonist, (-)-sulpiride, stimulated DA release in a concentration-dependent manner. The D-1 agonist, CY 20843, reversed the stimulatory effect of SCH 23390 but not that of (-)-sulpiride. It is concluded that D-1 and D-2 receptors located in the caudate control DA release separately in this area.

摘要

在自由活动的大鼠中,通过经纹状体透析探针局部应用D-1和D-2受体激动剂及拮抗剂,研究其对尾状核中多巴胺(DA)释放的影响。D-2激动剂(LY 171555和BHT 920)以浓度依赖性方式降低DA释放。局部应用氟哌啶醇可消除10微摩尔/升LY 171555和BHT 920的作用。一种特异性D-1激动剂,儿茶酚苯并氮䓬SKF 38393,可降低DA释放,且这种作用不受D-1拮抗剂SCH 23390全身或局部给药的影响,也不受D-2拮抗剂氟哌啶醇的影响。相反,非儿茶酚D-1激动剂CY 208243未能改变DA释放。局部应用D-1拮抗剂SCH 23390或D-2拮抗剂(-)-舒必利,以浓度依赖性方式刺激DA释放。D-1激动剂CY 20843可逆转SCH 23390的刺激作用,但不能逆转(-)-舒必利的刺激作用。结论是,位于尾状核的D-1和D-2受体在该区域分别控制DA释放。

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