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双侧6-羟基多巴胺损伤大鼠中,分别刺激多巴胺D-1和D-2受体所诱发的多动行为

Hyperactivity induced by stimulation of separate dopamine D-1 and D-2 receptors in rats with bilateral 6-OHDA lesions.

作者信息

Arnt J

出版信息

Life Sci. 1985 Aug 26;37(8):717-23. doi: 10.1016/0024-3205(85)90541-7.

Abstract

The effects of DA agonists and antagonists with different dopamine (DA) D-1 and D-2 receptor selectivity have been studied in rats with bilateral 6-OHDA lesions. The D-1 agonist SK & F 38393, the D-2 agonist pergolide and the mixed agonist apomorphine all induced marked hyperactivity in lesioned rats in doses which were without stimulant effect in sham-operated animals. The hyperactivity induced by SK & F 38393 was blocked by the DA D-1 antagonist SCH 23390, but unaffected by the D-2 antagonists spiroperidol or clebopride. Pergolide-induced hyperactivity showed the reverse selectivity. The mixed D-1/D-2 antagonists, cis(Z)-flupentixol and cis(Z)-clopenthixol, however blocked the effect of both agonists. Apomorphine-induced hyperactivity was neither blocked by selective D-1 nor D-2 antagonists, but was dose-dependently inhibited by cis(Z)-flupentixol and cis(Z)-clopenthixol. Potent blockade was also obtained by combined treatment with SCH 23390 and spiroperidol, indicating the need of blocking both D-1 and D-2 receptors simultaneously. The results indicate that D-1 and D-2 receptor function can be independently manipulated in denervated rats and they confirm similar results obtained in rats with unilateral 6-OHDA lesions using circling behaviour.

摘要

在双侧6-羟基多巴胺(6-OHDA)损伤的大鼠中,研究了具有不同多巴胺(DA)D-1和D-2受体选择性的DA激动剂和拮抗剂的作用。D-1激动剂SK&F 38393、D-2激动剂培高利特和混合激动剂阿扑吗啡,在假手术动物中无刺激作用的剂量下,均能诱导损伤大鼠出现明显的多动。SK&F 38393诱导的多动被DA D-1拮抗剂SCH 23390阻断,但不受D-2拮抗剂螺哌啶醇或氯氮平的影响。培高利特诱导的多动表现出相反的选择性。然而,混合的D-1/D-2拮抗剂顺式(Z)-氟哌噻吨和顺式(Z)-氯噻吨可阻断两种激动剂的作用。阿扑吗啡诱导的多动既不被选择性D-1拮抗剂也不被D-2拮抗剂阻断,但被顺式(Z)-氟哌噻吨和顺式(Z)-氯噻吨剂量依赖性抑制。联合使用SCH 23390和螺哌啶醇也可获得强效阻断作用,表明需要同时阻断D-1和D-2受体。结果表明,在去神经大鼠中,D-1和D-2受体功能可被独立调控,并且证实了在单侧6-OHDA损伤大鼠中利用转圈行为所获得的类似结果。

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