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多巴胺D1样受体激动剂对大鼠食物维持操作性行为的影响。

Effects of dopamine D1-like receptor agonists on food-maintained operant behavior in rats.

作者信息

Katz Jonathan L, Kopajtic Theresa A, Terry Philip

机构信息

Psychobiology Section, National Institute on Drug Abuse, Intramural Research Program, National Institutes of Health, Baltimore, Maryland 21224, USA.

出版信息

Behav Pharmacol. 2006 Jun;17(4):303-9. doi: 10.1097/01.fbp.0000205015.67079.f7.

Abstract

The effects on learned operant behavior of agonist actions at dopamine D1-like receptors have not been fully characterized. We compared three D1-like receptor agonists (SKF 38393, SKF 77434 and SKF 82958), both alone and in combination with the D1-like receptor antagonist, SCH 23390. Binding affinities for the agonists at dopamine D1 receptors from rat striatum membranes were determined and compared with effects on behavior. Lever pressing was maintained by food reinforcement under a fixed-ratio 30-response schedule (each 30th response produced reinforcement), and the effects of the three agonists were assessed by cumulative dosing. Each drug produced dose-related reductions in response rates, with an order of potency (SKF 82958>SKF 77434>SKF 38393) that agreed with rank order of binding affinities. Antagonism of these behavioral effects by SCH 23390 was only significant for SKF 82958; surprisingly, SCH 23390 enhanced the effects of SKF 38393. For SKF 82958, the antagonism was receptor subtype-specific, as the D2-like receptor antagonist spiperone was ineffective. The nonselective serotonergic antagonist metergoline produced a significant rightward shift of the SKF 38393 dose-response function, indicating effective antagonism, although the degree of antagonism was not dose-related. These results support the view that the behavioral effects of D1-like receptor agonists differ in their susceptibility to antagonism by D1-like receptor antagonists, and that some effects of SKF 38393 may be mediated by serotonergic activity rather than by activity at D1-like receptors.

摘要

多巴胺D1样受体激动剂对习得性操作行为的影响尚未完全明确。我们比较了三种D1样受体激动剂(SKF 38393、SKF 77434和SKF 82958)单独使用以及与D1样受体拮抗剂SCH 23390联合使用时的情况。测定了这些激动剂对大鼠纹状体膜多巴胺D1受体的结合亲和力,并将其与对行为的影响进行比较。在固定比率30次反应的强化程序下(每第30次反应产生强化)通过食物强化维持杠杆按压,通过累积给药评估三种激动剂的作用。每种药物均产生与剂量相关的反应率降低,其效价顺序(SKF 82958>SKF 77434>SKF 38393)与结合亲和力的排序一致。SCH 23390对这些行为效应的拮抗作用仅对SKF 82958有显著意义;令人惊讶的是,SCH 23390增强了SKF 38393的作用。对于SKF 82958,这种拮抗作用具有受体亚型特异性,因为D2样受体拮抗剂螺哌隆无效。非选择性5-羟色胺能拮抗剂麦角林使SKF 38393剂量-反应函数显著右移,表明有有效的拮抗作用,尽管拮抗程度与剂量无关。这些结果支持以下观点:D1样受体激动剂的行为效应在对D1样受体拮抗剂拮抗作用的敏感性方面存在差异,并且SKF 38393的某些效应可能是由5-羟色胺能活性介导的,而非D1样受体的活性。

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