Wilson Charles J, Weyrick Angela, Terman David, Hallworth Nicholas E, Bevan Mark D
Department of Biology, University of Texas at San Antonio, San Antonio, Texas 78249, USA.
J Neurophysiol. 2004 May;91(5):1963-80. doi: 10.1152/jn.00924.2003. Epub 2003 Dec 31.
Subthalamic nucleus neurons exhibit reverse spike-frequency adaptation. This occurs only at firing rates of 20-50 spikes/s and higher. Over this same frequency range, there is an increase in the steady-state frequency-intensity (F-I) curve's slope (the secondary range). Specific blockade of high-voltage activated calcium currents reduced the F-I curve slope and reverse adaptation. Blockade of calcium-dependent potassium current enhanced secondary range firing. A simple model that exhibited these properties used spike-triggered conductances similar to those in subthalamic neurons. It showed: 1) Nonaccumulating spike afterhyperpolarizations produce positively accelerating F-I curves and spike-frequency adaptation that is complete after the second spike. 2) Combinations of accumulating aftercurrents result in a linear F-I curve, whose slope depends on the relative contributions of inward and outward currents. Spike-frequency adaptation can be gradual. 3) With both accumulating and nonaccumulating aftercurrents, primary and secondary ranges will be present in the F-I curve. The slope of the primary range is determined by the nonaccumulating conductance; the accumulating conductances govern the secondary range. The transition is determined by the relative strengths of accumulating and nonaccumulating currents. 4) Spike-threshold accommodation contributes to the secondary range, reducing its slope at high firing rates. Threshold accommodation can stabilize firing when inward aftercurrents exceed outward ones. 5) Steady-state reverse adaptation results when accumulated inward aftercurrents exceed outward ones. This requires spike-threshold accommodation. Transient speedup arises when inward currents are smaller than outward ones at steady state, but accumulate more rapidly. 6) The same mechanisms alter firing in response to irregular patterns of synaptic conductances, as cell excitability fluctuates with changes in firing rate.
丘脑底核神经元表现出反向的放电频率适应性。这种现象仅在20 - 50次/秒及更高的放电频率下出现。在相同的频率范围内,稳态频率 - 强度(F - I)曲线的斜率会增加(第二范围)。特异性阻断高电压激活的钙电流会降低F - I曲线的斜率和反向适应性。阻断钙依赖性钾电流会增强第二范围的放电。一个展示这些特性的简单模型使用了类似于丘脑底核神经元的锋电位触发电导。它表明:1)非累积性的锋电位后超极化产生正加速的F - I曲线和在第二个锋电位后完成的放电频率适应性。2)累积性后电流的组合导致线性F - I曲线,其斜率取决于内向和外向电流的相对贡献。放电频率适应性可以是渐进的。3)同时存在累积性和非累积性后电流时,F - I曲线中将出现初级范围和次级范围。初级范围的斜率由非累积性电导决定;累积性电导控制次级范围。转变由累积性和非累积性电流的相对强度决定。4)锋电位阈值适应性对次级范围有贡献,在高放电频率下降低其斜率。当内向后电流超过外向后电流时,阈值适应性可以稳定放电。5)当累积的内向后电流超过外向后电流时会产生稳态反向适应性。这需要锋电位阈值适应性。当稳态时内向电流小于外向电流,但累积更快时会出现瞬态加速。6)相同的机制会改变对不规则突触电导模式的放电,因为细胞兴奋性会随着放电频率的变化而波动。