Univ. de Bordeaux, Institut des Maladies Neurodegeneratives, UMR 5293, F-33000, Bordeaux, France.
CNRS, Institut des Maladies Neurodegeneratives, UMR 5293, F-33000, Bordeaux, France.
Sci Rep. 2018 Jun 11;8(1):8858. doi: 10.1038/s41598-018-27195-6.
Corticofugal fibers target the subthalamic nucleus (STN), a component nucleus of the basal ganglia, in addition to the striatum, their main input. The cortico-subthalamic, or hyperdirect, pathway, is thought to supplement the cortico-striatal pathways in order to interrupt/change planned actions. To explore the previously unknown properties of the neurons that project to the STN, retrograde and anterograde tools were used to specifically identify them in the motor cortex and selectively stimulate their synapses in the STN. The cortico-subthalamic neurons exhibited very little sag and fired an initial doublet followed by non-adapting action potentials. In the STN, AMPA/kainate synaptic currents had a voltage-dependent conductance, indicative of GluA2-lacking receptors and were partly inhibited by Naspm. AMPA transmission displayed short-term depression, with the exception of a limited bandpass in the 5 to 15 Hz range. AMPA synaptic currents were negatively controlled by dopamine D5 receptors. The reduction in synaptic strength was due to postsynaptic D5 receptors, mediated by a PKA-dependent pathway, but did not involve a modified rectification index. Our data indicated that dopamine, through post-synaptic D5 receptors, limited the cortical drive onto STN neurons in the normal brain.
皮质传出纤维除了其主要输入的纹状体外,还靶向基底神经节的组成核团丘脑下核(STN)。皮质-丘脑下核(或超直接)通路被认为补充了皮质-纹状体通路,以中断/改变计划中的动作。为了探索投射到 STN 的神经元的先前未知特性,使用逆行和顺行工具在运动皮层中特异性地识别它们,并选择性地刺激它们在 STN 中的突触。皮质-丘脑下核神经元的凹陷很小,并且发出初始双脉冲,随后是非适应的动作电位。在 STN 中,AMPA/KA 突触电流具有电压依赖性电导,表明存在缺乏 GluA2 的受体,并且部分被 Naspm 抑制。AMPA 传递显示出短期抑制,除了在 5 到 15 Hz 范围内的有限通带之外。AMPA 突触电流受到多巴胺 D5 受体的负调控。突触强度的降低归因于突触后 D5 受体,通过 PKA 依赖性途径介导,但不涉及修改后的整流指数。我们的数据表明,多巴胺通过突触后 D5 受体,在正常大脑中限制了皮质对 STN 神经元的驱动。