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去髓鞘轴突传导要求的计算检验。

A computational test of the requirements for conduction in demyelinated axons.

机构信息

Department of Neurobiology, Duke University Medical Center, Durham, NC 27710 (U.S.A.).

出版信息

Restor Neurol Neurosci. 1991 Jan 1;3(2):81-93. doi: 10.3233/RNN-1991-3205.

Abstract

Conduction in demyelinated and remyelinating axons has been simulated with a computational model. The calculations made use of recent determinations of ionic channel densities in the internodal axolemma of Xenopus fibers. Several new morphological measurements reduced the number of parameters not directly obtained from experimental data. Action potentials and ionic currents were calculated for a wide range of fiber diameters and internodal lengths. The earliest stage of remyelination, characterized by Schwann cell attachment and extension of processes, was simulated by covering just a small percentage of the internode by a single cell layer. Conduction invariably failed if the internodal Na+ channel density was zero. The minimum density required for successful propagation agreed well with that measured in loose patch clamp experiments. Lateral diffusion of Na+ channels from nodes of Ranvier into the demyelinated internode did not restore conduction in blocked axons, and this was true regardless of the initial internodal Na+ channel density. Decreases in the internodal K+ channel density improved the safety factor for conduction, but this was significant only in the largest axons. Simulating minimal paranodal demyelination by eliminating the axo-glial junctional seals did not result in conduction block, but did produce large conduction delays.

摘要

脱髓鞘和髓鞘再生轴突的传导已经通过计算模型进行了模拟。这些计算利用了最近在非洲爪蟾纤维的节间轴突膜内离子通道密度的测定结果。几个新的形态学测量结果减少了不能直接从实验数据获得的参数数量。为广泛的纤维直径和节间长度范围计算了动作电位和离子电流。仅通过单层细胞覆盖节间的一小部分来模拟脱髓鞘的最早阶段,其特征是施旺细胞附着和过程延伸。如果节间 Na+通道密度为零,传导必然失败。成功传播所需的最小密度与在松散膜片钳实验中测量的密度非常吻合。来自郎飞结的 Na+通道从有髓鞘的节间向侧向扩散并没有恢复阻滞轴突的传导,无论初始节间 Na+通道密度如何,这都是正确的。节间 K+通道密度的降低提高了传导的安全系数,但仅在最大的轴突中才有意义。通过消除轴突-神经胶质连接密封来模拟最小的近郎飞结脱髓鞘并不会导致传导阻滞,但会导致较大的传导延迟。

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