Department of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Prog Brain Res. 2010;183:149-67. doi: 10.1016/S0079-6123(10)83008-0.
Dopamine (DA) is a key regulator of action selection and associative learning. The striatum has long been thought to be a major locus of DA action in this process. Although all striatal cell types express G protein-coupled receptors for DA, the effects of DA on principal medium spiny neurons (MSNs) understandably have received the most attention. In the two principal classes of MSN, DA receptor expression diverges, with striatonigral MSNs robustly expressing D(1) receptors and striatopallidal MSNs expressing D(2) receptors. In the last couple of years, our understanding of how these receptors and the intracellular signalling cascades that they couple to modulate dendritic physiology and synaptic plasticity has rapidly expanded, fuelled in large measure by the development of new optical and genetic tools. These tools also have enabled a rapid expansion of our understanding of the striatal adaptations in models of Parkinson's disease. This chapter highlights some of the major advances in these areas.
多巴胺(DA)是动作选择和联想学习的关键调节因子。纹状体长期以来一直被认为是该过程中 DA 作用的主要部位。尽管所有纹状体细胞类型都表达多巴胺 G 蛋白偶联受体,但多巴胺对主要中间神经元(MSN)的影响无疑受到了最多的关注。在两类主要的 MSN 中,DA 受体表达出现分歧,纹状体苍白球 MSN 强烈表达 D1 受体,而纹状体黑质 MSN 表达 D2 受体。在过去的几年中,我们对这些受体以及它们偶联的细胞内信号级联如何调节树突生理和突触可塑性的理解迅速扩展,在很大程度上得益于新的光学和遗传工具的发展。这些工具还使我们对帕金森病模型中纹状体适应性的理解迅速扩展。本章重点介绍了这些领域的一些重大进展。