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Toward whole-brain dopamine movies: a critical review of PET imaging of dopamine transmission in the striatum and cortex

机译:走向全脑多巴胺电影:对纹状体和皮层中多巴胺传播的PET成像的批判性评论

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摘要

The mesocorticolimbic dopamine (DA) circuit, comprising the mesolimbic and mesocortical DA pathways, plays a crucial role in reward, cognitive control, and motivation. The positron emission tomography (PET) radiotracer, [C-11]raclopride, has been used widely to image DA receptors and DA changes in the mesolimbic pathway before and after pharmacological and behavioral challenges. In certain circumstances, properties of traditional kinetic models—used to analyze dynamic PET data—are not well-suited to describing the effects of stimulus-induced DA release. To combat model shortcomings, the authors have advanced a suite of models that characterizes PET data in the presence of time-varying DA release. We review select [C-11]raclopride studies of the striatum during cigarette smoking to illustrate the advantages of such models. DA receptors occur in lower density in the cortex than the striatum. This, as well as higher relative background signal, poses a serious challenge to quantitative PET of DA changes in the mesocortical system. Novel high affinity radioligands [F-18]fallypride and [C-11]FLB457 have been used to image mesocortical DA transmission. Models with time-varying terms may also hold the key to optimizing sensitivity to changes in mesocortical DA. As an illustration, we compare recent PET studies of the effect of stress on cortical DA release. Finally, we consider some challenges and strategies for further optimization of sensitivity of PET to stimulus-induced DA changes throughout the whole brain.Electronic supplementary materialThe online version of this article (10.1007/s11682-017-9779-7) contains supplementary material, which is available to authorized users.
机译:中脑皮质多巴胺(DA)回路包括中脑边缘和中脑DA通路,在奖励,认知控制和动机中起着至关重要的作用。正电子发射断层扫描(PET)放射性示踪剂[C-11] raclopride,已广泛用于对药理学和行为挑战前后的DA受体和中脑边缘途径中的DA变化进行成像。在某些情况下,用于分析动态PET数据的传统动力学模型的属性不适用于描述刺激性DA释放的影响。为了克服模型缺陷,作者开发了一套模型,该模型可在存在随时间变化的DA发布的情况下表征PET数据。我们回顾了吸烟过程中纹状体的精选[C-11] raclopride研究,以说明此类模型的优势。 DA受体在皮质中的密度低于纹状体。这以及较高的相对本底信号对中皮层系统中DA变化的定量PET提出了严峻的挑战。新型高亲和力放射性配体[F-18]氟利昂和[C-11] FLB457已用于成像中皮层DA传输。具有时变项的模型也可能是优化对中皮层DA变化敏感性的关键。作为说明,我们比较了最近PET对应激对皮质DA释放的影响的研究。最后,我们考虑了进一步优化PET对全脑刺激引起的DA变化敏感性的挑战和策略。电子补充材料本文的在线版本(10.1007 / s11682-017-9779-7)包含补充材料,其中适用于授权用户。

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