Department of Neurodegeneration and Restorative Research, Center for Neurological Medicine, Göttingen, Germany.
J Neurochem. 2010 Jul;114(2):587-96. doi: 10.1111/j.1471-4159.2010.06788.x. Epub 2010 Apr 29.
The dopamine transporter (DAT) mediates dopamine uptake in many brain areas and has been suggested to underlie dopamine release in the substantia nigra pars reticulata. This release modulates basal ganglia output and motor performance. It is triggered by glutamatergic subthalamic afferents. We show here that activation of (G(q)-coupled) group I metabotropic glutamate receptors are sufficient to induce dopamine release in rat substantia nigra pars reticulata slices. Release was measured by amperometry and inhibited by a DAT antagonist. In a DAT-expressing cell line, dopamine release could be induced by activation of G(q)-coupled muscarinic receptors. Release was measured by HPLC and inhibited by a DAT antagonist. In both paradigms, activation of protein kinase C (PKC) was necessary and sufficient for dopamine release, suggesting that G(q)-coupled receptors can induce DAT-mediated dopamine release through PKC, and providing a physiological role for the known regulation of DAT-mediated release by PKC. Activation of muscarinic receptors and PKC also induced release from a cell line expressing the norepinephrine transporter, suggesting that transport-mediated release might be relevant in further brain areas.
多巴胺转运体(DAT)介导许多脑区的多巴胺摄取,并被认为是黑质网状部多巴胺释放的基础。这种释放调节基底神经节的输出和运动表现。它是由谷氨酸能丘脑下传入纤维触发的。我们在这里表明,(G(q) 偶联)第一组代谢型谷氨酸受体的激活足以诱导大鼠黑质网状部切片中的多巴胺释放。通过电流测定法测量释放,并被 DAT 拮抗剂抑制。在表达 DAT 的细胞系中,G(q) 偶联毒蕈碱受体的激活可以诱导多巴胺释放。通过 HPLC 测量释放,并被 DAT 拮抗剂抑制。在这两种模式中,蛋白激酶 C(PKC)的激活是多巴胺释放所必需且充分的,这表明 G(q) 偶联受体可以通过 PKC 诱导 DAT 介导的多巴胺释放,并为 PKC 对 DAT 介导的释放的已知调节提供生理作用。毒蕈碱受体和 PKC 的激活也诱导表达去甲肾上腺素转运体的细胞系释放,这表明转运体介导的释放可能与进一步的脑区有关。