Atherton Jeremy F, Wokosin David L, Ramanathan Sankari, Bevan Mark D
Department of Physiology, Feinberg School of Medicine, Northwestern University, 303 E. Chicago Avenue, Chicago, IL 60611, USA.
J Physiol. 2008 Dec 1;586(23):5679-700. doi: 10.1113/jphysiol.2008.155861. Epub 2008 Oct 2.
The activity of the subthalamic nucleus (STN) is intimately related to movement and is generated, in part, by voltage-dependent Na(+) (Na(v)) channels that drive autonomous firing. In order to determine the principles underlying the initiation and propagation of action potentials in STN neurons, 2-photon laser scanning microscopy was used to guide tight-seal whole-cell somatic and loose-seal cell-attached axonal/dendritic patch-clamp recordings and compartment-selective ion channel manipulation in rat brain slices. Action potentials were first detected in a region that corresponded most closely to the unmyelinated axon initial segment, as defined by Golgi and ankyrin G labelling. Following initiation, action potentials propagated reliably into axonal and somatodendritic compartments with conduction velocities of approximately 5 m s(-1) and approximately 0.7 m s(-1), respectively. Action potentials generated by neurons with axons truncated within or beyond the axon initial segment were not significantly different. However, axon initial segment and somatic but not dendritic or more distal axonal application of low [Na(+)] ACSF or the selective Na(v) channel blocker tetrodotoxin consistently depolarized action potential threshold. Finally, somatodendritic but not axonal application of GABA evoked large, rapid inhibitory currents in concordance with electron microscopic analyses, which revealed that the somatodendritic compartment was the principal target of putative inhibitory inputs. Together the data are consistent with the conclusions that in STN neurons the axon initial segment and soma express an excess of Na(v) channels for the generation of autonomous activity, while synaptic activation of somatodendritic GABA(A) receptors regulates the axonal initiation of action potentials.
丘脑底核(STN)的活动与运动密切相关,部分由驱动自主放电的电压依赖性钠(Na⁺)(Na(v))通道产生。为了确定STN神经元动作电位起始和传播的潜在机制,采用双光子激光扫描显微镜引导在大鼠脑片中进行紧密封全细胞体膜和松密封细胞贴附轴突/树突膜片钳记录以及隔室选择性离子通道操作。动作电位首先在与高尔基和锚蛋白G标记所定义的最接近无髓鞘轴突起始段的区域被检测到。起始后,动作电位分别以约5 m s⁻¹和约0.7 m s⁻¹的传导速度可靠地传播到轴突和体树突隔室。轴突在轴突起始段内或超出轴突起始段被截断的神经元产生的动作电位没有显著差异。然而,轴突起始段和胞体而非树突或更远端轴突施加低[Na⁺]的人工脑脊液(ACSF)或选择性Na(v)通道阻滞剂河豚毒素会持续使动作电位阈值去极化。最后,与电子显微镜分析一致,胞体树突而非轴突施加γ-氨基丁酸(GABA)会诱发大的、快速的抑制性电流,这表明胞体树突隔室是假定抑制性输入的主要靶点。这些数据共同支持以下结论:在STN神经元中,轴突起始段和胞体表达过量的Na(v)通道以产生自主活动,而胞体树突γ-氨基丁酸A(GABA(A))受体的突触激活调节动作电位的轴突起始。