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首页> 外文期刊>Psychopharmacology >Dopamine on D2-like receptors 'reboosts' dopamine D1-like receptor-mediated behavioural activation in rats licking for a isotonic NaCl solution
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Dopamine on D2-like receptors 'reboosts' dopamine D1-like receptor-mediated behavioural activation in rats licking for a isotonic NaCl solution

机译:D2样受体上的多巴胺“增强”舔等渗NaCl溶液的大鼠中的多巴胺D1样受体介导的行为激活

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Rationale: We recently suggested that dopamine on D1-like receptors is involved in the activation of goal-directed responses and the level of response activation is "reboosted" on the basis of an evaluation process involving D2-like receptors assessing "response efficacy". A main piece of evidence in support of this hypothesis was the observation of an "extinction mimicry" effect in the time course of licking bursts after dopamine D2-like receptor blockade in rats licking for sucrose. Objectives: The aim of this study was to determine whether the pattern of licking observed with sucrose as a reward could be reproduced in rats licking for a different reward (0.9 % NaCl). Materials and methods: We investigated the effects of the dopamine D1-like receptor antagonist SCH 23390 (0.01-0.04 mg/kg) and of the dopamine D2-like receptor antagonist raclopride (0.025-0.25 mg/kg) on the microstructure of licking for a 0.9 % NaCl solution in 12-h water-deprived rats in 30-min sessions. Results: As previously observed with sucrose as a reward, raclopride reduced the size of licking bursts and produced on the burst number time course an "extinction mimicry" effect, while SCH 23390 reduced licking exclusively by reducing burst number. Conclusions: These results are consistent with the proposed hypothesis and provide support to the use of the study of licking microstructure as a valid model not only for the investigation of the mechanisms governing ingestive behaviour but also for the investigation of the mechanisms underlying behavioural activation and the related evaluation processes.
机译:原理:我们最近建议,D1样受体上的多巴胺参与目标导向反应的激活,并且在涉及D2样受体的评估“反应功效”的评估过程的基础上,“增强”了反应激活的水平。支持该假设的主要证据是,在舔食蔗糖的大鼠中,在多巴胺D2样受体阻滞后的舔食爆发过程中观察到了“消光模仿”效应。目的:本研究的目的是确定以蔗糖作为奖励观察到的舔pattern模式是否可以在舔食不同奖励(0.9%NaCl)的大鼠中重现。材料和方法:我们研究了多巴胺D1样受体拮抗剂SCH 23390(0.01-0.04 mg / kg)和多巴胺D2样受体拮抗剂雷氯必利(0.025-0.25 mg / kg)对舔食的微观结构的影响。在30分钟内向缺水的12小时大鼠中加入0.9%NaCl溶液。结果:如先前用蔗糖作为奖励所观察到的,雷氯必利降低了舔burst的大小,并在猝发数的时间过程中产生了“消光模仿”效果,而SCH 23390仅通过减少猝发数来减少舔ing。结论:这些结果与所提出的假设是一致的,并为舔micro微观结构研究作为有效模型的使用提供了支持,该研究不仅用于研究控制吞咽行为的机制,而且还用于研究行为激活和行为机制的机制。相关评估流程。

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