The role of medial prefrontal cortical dopamine in spontaneous flexibility in the rat

M. Lanser, B. Ellenbroek, F. Zitman, D. Heeren, A. Cools
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引用次数: 17

Abstract

In rat studies, both lesions in the medial prefrontal cortex (mPFC) and alterations of the level of mPFC dopamine (DA) have been found to induce disturbances in behavioural flexibility, as measured with switching tasks. It is not clear whether mPFC DA is also involved in spontaneous flexibility. Therefore, the aim of the present study was to investigate the role of mPFC DA in spontaneous flexibility. As a measure for spontaneous flexibility, the diversity in spatial distribution of exploration on a large open field was used. The rats received local injections into the mPFC with a D 1 or D 2 antagonist, or the dopamimetic, amphetamine. The results showed that both DA antagonists reduced spontaneous flexibility, due to increased stimulus‐bound behaviour. Amphetamine had a similar effect to the DA antagonists. It is suggested that this is most likely due to an amphetamine‐induced increase in extracellular DA, leading to a suboptimal level of mPFC DA.
内侧前额叶皮层多巴胺在大鼠自发性柔韧性中的作用
在大鼠研究中,发现内侧前额叶皮层(mPFC)的损伤和mPFC多巴胺(DA)水平的改变都会引起行为灵活性的紊乱,这是通过切换任务来测量的。目前尚不清楚mPFC DA是否也参与自发柔韧性。因此,本研究的目的是探讨mPFC DA在自发柔韧性中的作用。作为一种自发灵活性的度量,在一个大的开放领域的勘探空间分布的多样性被使用。大鼠在mPFC局部注射d1或d2拮抗剂,或多巴胺类药物安非他明。结果表明,由于刺激结合行为增加,两种DA拮抗剂都降低了自发柔韧性。安非他明与DA拮抗剂的效果相似。这很可能是由于安非他明诱导的细胞外DA增加,导致mPFC DA低于最佳水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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