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D2 dopamine receptors modulate neuronal resonance in subthalamic nucleus and cortical high-voltage spindles through HCN channels

机译:D2多巴胺受体通过HCN通道调节亚粒细胞核中的神经元共振和皮质高压锭子

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The high-voltage spindles (HVSs), one of the characteristic oscillations that include theta frequencies in the basal ganglia (BG)-cortical system, are involved in immobile behavior and show increasing power in Parkinson's disease (PD). Our previous results suggested that the D2 dopamine receptor might be involved in HVSs modulations in a rat model of PD. Membrane resonance is one of the cellular mechanisms of network oscillation; therefore, we investigated how dopamine modulates the theta frequency membrane resonance of neurons in the subthalamic nucleus (STN), a central pacemaker of BG, and whether such changes in STN neurons subsequently alter HVSs in the BG-cortical system. In particular, we tested whether dopamine modulates HVSs through hyperpolarization-activated cyclic nucleotide gated (HCN) channels-dependent membrane resonance in STN neurons. We found that an antagonist of D2 receptors, but not of D1 receptors, inhibited membrane resonance and HCN currents of STN neurons through a G-protein activity in acute brain slices. Our further in vivo experiments using local injection of a D2 receptor antagonist or an HCN blocker in STNS of free-moving rats showed an increase in HVSs power and correlation in the BG-cortical system. Local injection of lamotrigine, an HCN agonist, counteracted the effect induced by the D2 antagonist. Taken together, our results revealed a potential cellular mechanism underlying HVSs activity modulation in the BG-cortical system, i.e. tuning HCN activities in STN neurons through dopamine D2 receptors. Our findings might lead to a new direction in PD treatment by providing promising new drug targets for HVSs activity modulation. (C) 2016 Elsevier Ltd. All rights reserved.
机译:高压主轴(HVSS)是基础神经节(BG)-Coric系统中的频率的特征振荡之一,涉及固定行为,并显示出帕金森病(PD)的增加的力量。我们以前的结果表明D2多巴胺受体可能参与PD大鼠模型中的HVSS调制。膜共振是网络振荡的蜂窝机制之一;因此,我们研究了多巴胺如何调节亚粒细胞核(STN),BG的中央起搏器中神经元的θ频率膜共振,以及STN神经元的这种变化随后在BG-皮质系统中改变HVSS。特别是,我们测试多巴胺是否通过在STN神经元中通过超极化激活的循环核苷酸所依赖于超极化活化的循环核苷酸所依赖的膜共振调节HVS。我们发现D2受体的拮抗剂,但不是D1受体,通过急性脑切片中的G蛋白活性抑制STN神经元的膜共振和HCN电流。我们在自由移动大鼠STN中使用局部注射D2受体拮抗剂或HCN阻断剂​​的体内实验表明,BG-皮质系统中的HVSS功率和相关性增加。局部注射乳草甲酰胺,HCN激动剂,抵消D2拮抗剂诱导的效果。我们的结果揭示了BG-皮质系统中HVSS活性调节的潜在细胞机制,即通过多巴胺D2受体调节STN神经元中的HCN活性。我们的发现可能通过为HVSS活性调制提供有希望的新药物目标来导致PD治疗中的新方向。 (c)2016 Elsevier Ltd.保留所有权利。

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