Somjen G G, Kager H, Wadman W J
Department of Cell Biology, Duke University Medical Center, Box 3011, Durham, NC 27710, USA.
J Comput Neurosci. 2009 Feb;26(1):139-47. doi: 10.1007/s10827-008-0103-9. Epub 2008 Jun 18.
As described by others, an extracellular calcium-sensitive non-selective cation channel (Ca(2+)-sensitive NSCC) of central neurons opens when extracellular calcium level decreases. An other non-selective current is activated by rising intracellular calcium (Ca(2+)). The Ca(2+)-sensitive NSCC is not dependent on voltage and while it is permeable by monovalent cations, it is blocked by divalent cations. We tested the hypothesis that activation of this channel can promote seizures and spreading depression (SD). We used a computer model of a neuron surrounded by interstitial space and enveloped in a glia-endothelial "buffer" system. Na(+), K(+), Ca(2+) and Cl(-) concentrations, ion fluxes and osmotically driven volume changes were computed. Conventional ion channels and the NSCC were incorporated in the neuron membrane. Activation of NSCC conductance caused the appearance of paroxysmal afterdischarges (ADs) at parameter settings that did not produce AD in the absence of NSCC. The duration of the AD depended on the amplitude of the NSCC. Similarly, NSCC also enabled the generation of SD. We conclude that NSCC can contribute to the generation of epileptiform events and to spreading depression.
正如其他人所描述的,中枢神经元的一种细胞外钙敏感非选择性阳离子通道(Ca(2+)敏感NSCC)在细胞外钙水平降低时开放。另一种非选择性电流由细胞内钙升高(Ca(2+))激活。Ca(2+)敏感NSCC不依赖电压,虽然它可通透单价阳离子,但被二价阳离子阻断。我们检验了该通道的激活可促进癫痫发作和扩散性抑制(SD)的假说。我们使用了一个被细胞间质包围并包裹在神经胶质-内皮“缓冲”系统中的神经元计算机模型。计算了Na(+)、K(+)、Ca(2+)和Cl(-)浓度、离子通量以及渗透驱动的体积变化。常规离子通道和NSCC被纳入神经元膜中。在没有NSCC时不会产生阵发性放电(AD)的参数设置下,NSCC电导的激活导致了阵发性后放电(AD)的出现。AD的持续时间取决于NSCC的幅度。同样,NSCC也能引发SD。我们得出结论,NSCC可促成癫痫样事件的产生和扩散性抑制。