Dipartimento di Scienze Biomediche, Università di Sassari, Viale San Pietro 43/B, 07100, Sassari, Italy.
Psychopharmacology (Berl). 2013 Sep;229(2):357-66. doi: 10.1007/s00213-013-3110-0. Epub 2013 Apr 30.
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.
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).
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.
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.
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.
我们最近提出,多巴胺 D1 样受体参与了目标导向反应的激活,而反应激活的水平是基于涉及 D2 样受体评估“反应效能”的评估过程而“重新增强”的。支持这一假设的一个主要证据是,在大鼠舔食蔗糖时,多巴胺 D2 样受体阻断后舔食爆发的时间进程中观察到了“消退模拟”效应。
本研究的目的是确定在以不同奖励(0.9%NaCl)为奖励的情况下,观察到的舔食模式是否可以在舔食大鼠中重现。
我们研究了多巴胺 D1 样受体拮抗剂 SCH 23390(0.01-0.04mg/kg)和多巴胺 D2 样受体拮抗剂氯丙嗪(0.025-0.25mg/kg)对 12 小时水剥夺大鼠在 30 分钟内舔食 0.9%NaCl 溶液的微观结构的影响。
正如之前观察到的蔗糖作为奖励一样,氯丙嗪减少了舔食爆发的大小,并在爆发数量的时间进程中产生了“消退模拟”效应,而 SCH 23390 则通过减少爆发数量来减少舔食。
这些结果与提出的假设一致,并为使用舔食微观结构研究提供了支持,不仅可以作为研究摄食行为的机制,还可以作为研究行为激活及其相关评估过程的机制。