Suppr超能文献

多巴胺D-1与D-2受体激动剂之间的协同相互作用:半横断大鼠的转圈行为

Synergistic interaction between dopamine D-1 and D-2 receptor agonists: circling behaviour of rats with hemitransection.

作者信息

Arnt J, Perregaard J

机构信息

Department of Pharmacology, H. Lundbeck A/S, Copenhagen, Denmark.

出版信息

Eur J Pharmacol. 1987 Nov 3;143(1):45-53. doi: 10.1016/0014-2999(87)90733-3.

Abstract

Circling behaviour induced by dopamine (DA) agonists with different D-1/D-2 receptor selectivity was studied in rats with hemitransection at a level caudal to the striatum. The mixed D-1/D-2 agonist apomorphine induced ipsilateral circling behaviour after administration of doses similar to those that induced stereotyped behaviour in unlesioned rats. The effect of apomorphine was not influenced by co-treatment with SK & F 38393 or quinpirole, indicating that apomorphine induces a comparable D-1 and D-2 receptor stimulation in vivo also. Three selective D-1 agonists, SK & F 38393, SK & F 75670 and Lu 24-040 had no effects alone, while the preferential D-2 agonists quinpirole, pergolide and (-)-N-propylnorapomorphine induced ipsilateral circling of weaker intensity than did apomorphine. After co-treatment with SK & F 38393 the effects of these compounds were markedly increased. Combination of SK & F 38393, SK & F 75670 or Lu 24-040 with quinpirole induced circling with intensities similar to those seen after apomorphine. Pretreatment with the D-1 antagonist SCH 23390 or the D-2 antagonist YM 09151-2 completely antagonized the ipsilateral circling induced by either apomorphine or quinpirole + SK & F 38393. A range of partial (autoreceptor) D-2 agonists, i.e. (-)-3-PPP, (+)-3-phenethyl-PP, terguride, EMD 23448 and B-HT 920 were all ineffective as was the alpha 2-adrenoceptor agonist clonidine. However, B-HT 920 induced strong ipsilateral circling after combination with SK & F 38393, whereas (-)-3-PPP was ineffective.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在纹状体尾侧水平进行半横断的大鼠中,研究了具有不同D-1/D-2受体选择性的多巴胺(DA)激动剂诱导的转圈行为。混合的D-1/D-2激动剂阿扑吗啡在给予与在未损伤大鼠中诱导刻板行为相似的剂量后,诱导同侧转圈行为。阿扑吗啡的作用不受与SK&F 38393或喹吡罗联合治疗的影响,这表明阿扑吗啡在体内也能诱导相当的D-1和D-2受体刺激。三种选择性D-1激动剂SK&F 38393、SK&F 75670和Lu 24-040单独使用均无作用,而优先的D-2激动剂喹吡罗、培高利特和(-)-N-丙基去甲阿扑吗啡诱导的同侧转圈强度比阿扑吗啡弱。与SK&F 38393联合治疗后,这些化合物的作用明显增强。SK&F 38393、SK&F 75670或Lu 24-040与喹吡罗联合诱导的转圈强度与阿扑吗啡后观察到的相似。用D-1拮抗剂SCH 23390或D-2拮抗剂YM 09151-2预处理可完全拮抗阿扑吗啡或喹吡罗+SK&F 38393诱导同侧转圈。一系列部分(自受体)D-2激动剂,即(-)-3-PPP、(+)-3-苯乙基-PP、特古瑞得、EMD 23448和B-HT 920均无效,α2-肾上腺素能受体激动剂可乐定也无效。然而,B-HT 920与SK&F 38393联合后诱导强烈的同侧转圈,而(-)-3-PPP无效。(摘要截断于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验