Department of Pharmacology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA; Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Department of Pharmacology, Columbia University, New York, NY 10032, USA.
Neuron. 2018 May 2;98(3):575-587.e4. doi: 10.1016/j.neuron.2018.03.038. Epub 2018 Apr 12.
Dopamine input to the dorsal and ventral striatum originates from separate populations of midbrain neurons. Despite differences in afferent inputs and behavioral output, little is known about how dopamine release is encoded by dopamine receptors on medium spiny neurons (MSNs) across striatal subregions. Here we examined the activation of D2 receptors following the synaptic release of dopamine in the dorsal striatum (DStr) and nucleus accumbens (NAc) shell. We found that D2 receptor-mediated synaptic currents were slower in the NAc and this difference occurred at the level of D2-receptor signaling. As a result of preferential coupling to Gαo, we also found that D2 receptors in MSNs demonstrated higher sensitivity for dopamine in the NAc. The higher sensitivity in the NAc was eliminated following cocaine exposure. These results identify differences in the sensitivity and timing of D2-receptor signaling across the striatum that influence how nigrostriatal and mesolimbic signals are encoded across these circuits.
多巴胺输入到背侧纹状体和腹侧纹状体起源于中脑神经元的不同群体。尽管传入输入和行为输出存在差异,但对于多巴胺受体在纹状体亚区的中型多棘神经元(MSNs)上如何编码多巴胺释放知之甚少。在这里,我们研究了背侧纹状体(DStr)和伏隔核壳(NAc)中多巴胺突触释放后 D2 受体的激活。我们发现,NAc 中的 D2 受体介导的突触电流较慢,这种差异发生在 D2 受体信号传递的水平上。由于优先与 Gαo 偶联,我们还发现 MSNs 中的 D2 受体对 NAc 中的多巴胺具有更高的敏感性。可卡因暴露后,NAc 中的这种高敏感性被消除。这些结果表明,纹状体中 D2 受体信号的敏感性和时间存在差异,这会影响黑质纹状体和中脑边缘信号在这些回路中的编码方式。