De Schutter E
Born-Bunge Foundation, University of Antwerp-UIA, B2610 Antwerp, Belgium.
J Neurophysiol. 1998 Aug;80(2):504-19. doi: 10.1152/jn.1998.80.2.504.
The dendrites of most neurons express several types of voltage and Ca2+-gated channels. These ionic channels can be activated by subthreshold synaptic input, but the functional role of such activations in vivo is unclear. The interaction between dendritic channels and synaptic background input as it occurs in vivo was studied in a realistic computer model of a cerebellar Purkinje cell. It previously was shown using this model that dendritic Ca2+ channels amplify the somatic response to synchronous excitatory inputs. In this study, it is shown that dendritic ion channels also increased the somatic membrane potential fluctuations generated by the background input. This amplification caused a highly variable somatic excitatory postsynaptic potential (EPSP) in response to a synchronous excitatory input. The variability scaled with the size of the response in the model with excitable dendrite, resulting in an almost constant coefficient of variation, whereas in a passive model the membrane potential fluctuations simply added onto the EPSP. Although the EPSP amplitude in the active dendrite model was quite variable for different patterns of background input, it was insensitive to changes in the timing of the synchronous input by a few milliseconds. This effect was explained by slow changes in dendritic excitability. This excitability was determined by how the background input affected the dendritic membrane potentials in the preceding 10-20 ms, causing changes in activation of voltage and Ca2+-gated channels. The most important model variables determining the excitability at the time of a synchronous input were the Ca2+-activation of K+ channels and the inhibitory synaptic conductance, although many other model variables could be influential for particular background patterns. Experimental evidence for the amplification of postsynaptic variability by active dendrites is discussed. The amplification of the variability of EPSPs has important functional consequences in general and for cerebellar Purkinje cells specifically. Subthreshold, background input has a much larger effect on the responses to coherent input of neurons with active dendrites compared with passive dendrites because it can change the effective threshold for firing. This gives neurons with dendritic calcium channels an increased information processing capacity and provides the Purkinje cell with a gating function.
大多数神经元的树突表达几种类型的电压门控通道和钙门控通道。这些离子通道可被阈下突触输入激活,但其在体内这种激活的功能作用尚不清楚。在一个逼真的小脑浦肯野细胞计算机模型中研究了树突通道与体内发生的突触背景输入之间的相互作用。此前使用该模型表明,树突钙通道可放大躯体对同步兴奋性输入的反应。在本研究中,结果表明树突离子通道也增加了由背景输入产生的躯体膜电位波动。这种放大导致在对同步兴奋性输入的反应中,躯体兴奋性突触后电位(EPSP)高度可变。在具有可兴奋树突的模型中,这种可变性与反应大小成比例,导致变异系数几乎恒定,而在被动模型中,膜电位波动只是简单地叠加在EPSP上。尽管在主动树突模型中,对于不同模式的背景输入,EPSP幅度变化很大,但它对同步输入时间几毫秒的变化不敏感。这种效应是由树突兴奋性的缓慢变化来解释的。这种兴奋性取决于背景输入在之前10 - 20毫秒内如何影响树突膜电位,从而导致电压门控通道和钙门控通道激活的变化。决定同步输入时兴奋性的最重要模型变量是钾通道的钙激活和抑制性突触电导,尽管许多其他模型变量可能对特定背景模式有影响。文中讨论了主动树突放大突触后可变性的实验证据。一般来说,尤其是对于小脑浦肯野细胞,EPSP可变性的放大具有重要的功能后果。与被动树突相比,阈下背景输入对具有主动树突的神经元对相干输入的反应影响要大得多,因为它可以改变放电的有效阈值。这赋予具有树突钙通道的神经元更大的信息处理能力,并为浦肯野细胞提供一种门控功能。