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多巴胺 D1 样和 D2 样受体在强迫游泳试验中行为激活和反应效能评价中的可能作用。

Possible role of dopamine D1-like and D2-like receptors in behavioural activation and evaluation of response efficacy in the forced swimming test.

机构信息

Dipartimento di Scienze del Farmaco, Università di Sassari, Sassari, Italy.

出版信息

Neuropharmacology. 2012 Mar;62(4):1717-29. doi: 10.1016/j.neuropharm.2011.11.018. Epub 2011 Dec 6.

Abstract

Based on the different effects of the dopamine D1-like and D2-like receptor antagonists SCH 23390 and raclopride on the measures of licking microstructure in rats ingesting a sucrose solution, we suggested that the behavioural activation of reward-associated responses depends on dopamine D1-like receptor stimulation, and its level is updated, or "reboosted", on the basis of a dopamine D2-like receptor-mediated evaluation process. The aim of this study was to test this hypothesis on the forced swimming test response. The effects of the dopamine D1-like and D2-like receptor antagonists SCH 23390 (0.01-0.04 mg/kg) and raclopride (0.025-0.25 mg/kg) administered before a 15-min exposure to forced swimming, and the response to a second session performed 24 h later, were examined. SCH 23390 dose-dependently reduced climbing scores in the first session and increased them in the second session, but the within-session decline of this measure was similar to that observed in the control group in both sessions. Raclopride-treated subjects showed a slightly reduced level of climbing scores at the beginning of the first session, but persisted in emitting this costly behavioural response up to the end of the session, while no effects were observed in the second session. These results, along with our results examining licking for sucrose, are consistent with the hypothesis that behavioural activation and response effort allocation are directly mediated by dopamine D1-like receptor stimulation, but the level of this activation is updated, or "reboosted", on the basis of a dopamine D2-like receptor-mediated mechanism of response efficacy evaluation.

摘要

基于多巴胺 D1 样和 D2 样受体拮抗剂 SCH 23390 和 raclopride 对摄入蔗糖溶液的大鼠舔舐微观结构测量的不同影响,我们认为与奖励相关的反应的行为激活取决于多巴胺 D1 样受体的刺激,并且其水平基于多巴胺 D2 样受体介导的评估过程进行更新或“重新增强”。本研究的目的是在强迫游泳试验反应中检验这一假设。多巴胺 D1 样和 D2 样受体拮抗剂 SCH 23390(0.01-0.04mg/kg)和 raclopride(0.025-0.25mg/kg)在 15 分钟强迫游泳暴露前给药,以及对 24 小时后进行的第二次试验的反应进行了检查。SCH 23390 剂量依赖性地降低了第一阶段的攀爬分数,并在第二阶段增加了攀爬分数,但该措施在两次试验中均类似于对照组的试验结果。接受 raclopride 治疗的对象在第一阶段开始时攀爬分数略有降低,但在整个阶段仍持续发出这种代价高昂的行为反应,而在第二阶段则没有观察到影响。这些结果与我们检查蔗糖舔舐的结果一致,表明行为激活和反应努力分配直接由多巴胺 D1 样受体刺激介导,但这种激活的水平基于多巴胺 D2 样受体介导的反应效能评估机制进行更新或“重新增强”。

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