Teixeira Hewerson Z, Almeida Antônio-Carlos G, Infantosi Antonio F C, Rodrigues Antônio M, Costa Natália L, Duarte Mário A
Laboratory of Experimental and Computational Neuroscience, Biomedical Engineering Department, Federal University of São João del-Rei, São João del-Rei-MG-36.301-160, Brazil.
Comput Biol Chem. 2008 Aug;32(4):273-81. doi: 10.1016/j.compbiolchem.2008.03.011. Epub 2008 Apr 1.
A mathematical description of the restoring ionic mechanisms in a compartmentalized electrochemical model of neuronal tissues was developed aiming at studying the essential conditions for refractoriness of Leão's spreading depression (SD). The model comprehends the representation of a plexiform layer, composed by synaptic terminals and glial process immersed in an extracellular space where the space-temporal variations of the ionic concentrations were described by electrodiffusion equations. The synaptic transmission was described by differential equations representing the corresponding chemical reactions associated with the neurotransmitter release, diffusion, binding to its receptor in the postsynaptic membrane and the uptake by the presynaptic terminals. The effect of the neurotransmitter binding to the receptor induces changes in the permeability of the postsynaptic membrane and the corresponding transmembrane fluxes were calculated. The fluxes promote changes in the external ionic concentrations, changing the ionic electrodiffusion through the extracellular space. The description of these mechanisms provides the reaction-diffusion structure of the model and allows simulating the wave propagation. The simulations of experimental maneuvers of application of two consecutive stimuli for inducing SD suggest: (i) the extracellular space acts coupling the postsynaptic terminals and glial cells recovery mechanisms in such a way that the extracellular ionic concentrations change only during the wave front; (ii) the potassium removed from the extracellular by the glial cells, originated from the depolarization of the synaptic terminals returns slowly limited by the glial release, contributing for the refractoriness of the tissue; (iii) critical points for sodium and potassium transmembrane fluxes could be identified, allowing proposing specific conditions for the interplay between channels and pumps fluxes for determining the absolute and relative refractory periods.
为了研究莱奥扩散性抑制(SD)不应期的基本条件,我们建立了一个神经元组织的分区电化学模型中恢复离子机制的数学描述。该模型包含了一个丛状层的表示,它由突触终末和浸入细胞外空间的神经胶质突起组成,其中离子浓度的时空变化由电扩散方程描述。突触传递由微分方程描述,这些方程表示与神经递质释放、扩散、与突触后膜上受体结合以及突触前终末摄取相关的化学反应。神经递质与受体结合的效应诱导突触后膜通透性的变化,并计算相应的跨膜通量。这些通量促进细胞外离子浓度的变化,改变通过细胞外空间的离子电扩散。对这些机制的描述提供了模型的反应扩散结构,并允许模拟波的传播。对施加两个连续刺激以诱导SD的实验操作的模拟表明:(i)细胞外空间以这样一种方式耦合突触后终末和神经胶质细胞的恢复机制,即细胞外离子浓度仅在波前期间发生变化;(ii)神经胶质细胞从细胞外去除的钾,源于突触终末的去极化,由于神经胶质释放的限制而缓慢返回,这有助于组织的不应期;(iii)可以确定钠和钾跨膜通量的临界点,从而提出通道和泵通量之间相互作用的特定条件,以确定绝对和相对不应期。