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多巴胺激动剂增加了持续的工具性反应,但不能恢复帕金森病大鼠模型中的习惯形成。

Dopamine agonists increase perseverative instrumental responses but do not restore habit formation in a rat model of Parkinsonism.

机构信息

CNRS, UMR 8195, Orsay, France.

出版信息

Neuroscience. 2010 Jun 30;168(2):477-86. doi: 10.1016/j.neuroscience.2010.03.047. Epub 2010 Apr 1.

Abstract

Dopamine (DA) deafferentation of the dorsolateral striatum has been shown to prevent habit development, leaving instrumental behavior under action-outcome control that is persistently sensitive to modification of the motivational value of the reward. The present experiment further explored the basis of this dysfunction by examining the ability of intrastriatal DA agonist injections (D1 SKF 38393 or D2/D3 Quinpirole) during overtraining of a signaled instrumental task to restore habit formation in rats subjected to bilateral 6-hydroxydopamine (6-OHDA) lesions of the nigrostriatal dopaminergic pathway. Overtraining was followed by a test of goal sensitivity by satiety-specific devaluation of the reward. The results confirmed the impaired shift in performance from action to habit in control lesioned rats. However, lesioned rats repeatedly injected with quinpirole D2/D3 agonist showed an increase in non-rewarded instrumental responses (intertrials periods) during overtraining, suggesting the development of perseverative behavior. Following the procedure of devaluation, quinpirole D2/D3 agonist treatment, and to a lesser extent SKF 38393 D1 agonist, caused the persistence of sensitivity to reward devaluation, indicating clear goal-directed behavior despite extended training. This absence of restoration of habit formation by DA agonist treatment is discussed in the light of DA agonist effects in Parkinson patients.

摘要

背外侧纹状体的多巴胺(DA)去传入已被证明可以防止习惯的形成,从而使工具性行为受到动作-结果控制,而这种控制仍然容易受到奖励动机价值改变的影响。本实验进一步通过检查在信号化工具任务过度训练期间向纹状体内注射多巴胺激动剂(D1 SKF 38393 或 D2/D3 Quinpirole)的能力,来探究这种功能障碍的基础,以恢复接受双侧 6-羟多巴胺(6-OHDA)黑质纹状体多巴胺能通路损伤的大鼠的习惯形成。过度训练后,通过奖励的饱腹感特异性贬值来测试目标敏感性。结果证实,在对照损伤的大鼠中,从动作到习惯的表现转变受损。然而,反复注射 Quinpirole D2/D3 激动剂的损伤大鼠在过度训练期间表现出非奖励性工具反应(试验间期)增加,表明出现了持续性行为。在贬值程序、Quinpirole D2/D3 激动剂治疗之后,以及在较小程度上 D1 激动剂 SKF 38393 之后,会导致对奖励贬值的敏感性持续存在,这表明尽管经过了长时间的训练,但仍存在明确的目标导向行为。尽管进行了多巴胺激动剂治疗,但仍未恢复习惯形成,这一现象与帕金森病患者中多巴胺激动剂的作用有关。

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