The Leslie and Susan Gonda Interdisciplinary Brain Research Center, Bar Ilan University, 52900, Ramat Gan, Israel.
The Mina and Everard Goodman Faculty of Life Sciences, Bar Ilan University, 52900, Ramat Gan, Israel.
Brain Struct Funct. 2018 Jul;223(6):2673-2684. doi: 10.1007/s00429-018-1657-6. Epub 2018 Mar 22.
Dopamine is critical for the normal functioning of the basal ganglia, modulating both input and output nuclei of this system. The distribution and function of each of the five dopamine receptor subtypes have been studied extensively in the striatum. However, the role of extrastriatal dopamine receptors in basal ganglia information processing is less clear. Here, we studied the anatomical distribution of dopamine receptors in one of the output nuclei of the rodent basal ganglia, the entopeduncular nucleus (EP). The presence of all dopamine receptor subtypes was verified in the EP using immunostaining. We detected co-localization of dopamine receptors with VGAT, which suggests presynaptic expression on GABAergic terminals. D1R and D2R were strongly colocalized with VGAT, whereas DR3-5 showed only sparse co-localization. We further labeled striatal or pallidal neurons with GFP and showed that only D1 receptors were co-localized with striatal terminals, while only D2R and D3R were co-localized with pallidal terminals. Dopamine receptors were also strongly co-localized with MAP2, indicating postsynaptic expression. Overall, these findings suggest that the dopaminergic system modulates activity in the EP both directly via postsynaptic receptors, and indirectly via GABAergic synapses stemming from the direct and indirect pathways.
多巴胺对于基底神经节的正常功能至关重要,调节着该系统的输入和输出核团。在纹状体中,已经广泛研究了五种多巴胺受体亚型中的每一种的分布和功能。然而,纹状体以外的多巴胺受体在基底神经节信息处理中的作用尚不清楚。在这里,我们研究了多巴胺受体在啮齿动物基底神经节的一个输出核团——红核脚间核(EP)中的解剖分布。使用免疫染色法证实了 EP 中存在所有五种多巴胺受体亚型。我们检测到多巴胺受体与 VGAT 的共定位,这表明它们在 GABA 能末梢上有突触前表达。D1R 和 D2R 与 VGAT 强烈共定位,而 DR3-5 仅显示稀疏的共定位。我们进一步用 GFP 标记纹状体或苍白球神经元,并表明只有 D1 受体与纹状体末梢共定位,而只有 D2R 和 D3R 与苍白球末梢共定位。多巴胺受体也与 MAP2 强烈共定位,表明其具有突触后表达。总的来说,这些发现表明,多巴胺能系统通过突触后受体直接调节 EP 的活动,并且通过来自直接和间接通路的 GABA 能突触间接调节 EP 的活动。