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用 Griffonia simplicifolia isolectin IB4 区分大鼠小直径初级感觉神经元的兴奋性参数和对海葵毒素 ATX-II 的敏感性。

Excitability parameters and sensitivity to anemone toxin ATX-II in rat small diameter primary sensory neurones discriminated by Griffonia simplicifolia isolectin IB4.

机构信息

Queen Mary University of London, Barts and The London School of Medicine and Dentistry, Neuroscience and Trauma Centre, Blizard Institute of Cell and Molecular Science, London E1 2AT, UK.

出版信息

J Physiol. 2010 Jan 1;588(Pt 1):125-37. doi: 10.1113/jphysiol.2009.181107. Epub 2009 Nov 9.

DOI:10.1113/jphysiol.2009.181107
PMID:19900960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2821554/
Abstract

Sensory neurone subtypes (< or = 25 microm apparent diameter) express a variety of Na(+) channels, where expression is linked to action potential duration, and associated with differential IB4-lectin binding. We hypothesized that sensitivity to ATX-II might also discriminate neurones and report that 1 microm has negligible or small effects on action potentials in IB4 +ve, but dramatically increased action potential duration in IB4 ve, neurones. The toxin did not act on tetrodotoxin-resistant (TTX-r) Na(V)1.8 currents; discrimination was based on tetrodotoxin-sensitive (TTX-s) Na(+) channel expression. We also explored the effects of varying the holding potential on current threshold, and the effect of repetitive activation on action currents in IB4 +ve and ve neurones. IB4 +ve neurones became more excitable with depolarization over the range 100 to 20 mV, but IB4 ve neurones exhibited peak excitability near 55 mV, and were inexcitable at 20 mV. Eliciting action potentials at 2 Hz, we found that peak inward action current in IB4 +ve neurones was reduced, whereas changes in the current amplitude were negligible in most IB4 ve neurones. Our findings are consistent with relatively toxin-insensitive channels including Na(V)1.7 being expressed in IB4 +ve neurones, whereas toxin sensitivity indicates that IB4 ve neurones may express Na(V)1.1 or Na(V)1.2, or both. The retention of excitability at low membrane potentials, and the responses to repetitive stimulation are explained by the known preferential expression of Na(V)1.8 in IB4 +ve neurones, and the reduction in action current in IB4 +ve neurones with repetitive stimulation supports a novel hypothesis explaining the slowing of conduction velocity in C-fibres by the build-up of Na(+) channel inactivation.

摘要

感觉神经元亚型(<或=25 微米表观直径)表达多种钠离子通道,其表达与动作电位持续时间相关,并与 IB4- 凝集素结合的差异相关。我们假设 ATX-II 的敏感性也可能区分神经元,并报告 1 微米对 IB4+阳性神经元的动作电位几乎没有或有较小的影响,但对 IB4-阴性神经元的动作电位持续时间有显著增加。毒素对河豚毒素抗性(TTX-r)钠通道(Na(V)1.8 电流)没有作用;区分基于河豚毒素敏感(TTX-s)钠离子通道的表达。我们还探讨了改变保持电位对电流阈值的影响,以及重复激活对 IB4+阳性和阴性神经元动作电流的影响。IB4+阳性神经元在 100 至 20 mV 范围内去极化时兴奋性增加,但 IB4-阴性神经元的峰值兴奋性接近 55 mV,在 20 mV 时兴奋性消失。以 2 Hz 的频率引发动作电位,我们发现 IB4+阳性神经元的内向动作电流峰值减小,而大多数 IB4-阴性神经元的电流幅度变化可以忽略不计。我们的发现与相对不敏感的通道一致,包括 Na(V)1.7 在内的通道在 IB4+阳性神经元中表达,而毒素敏感性表明 IB4-阴性神经元可能表达 Na(V)1.1 或 Na(V)1.2,或两者兼有。低膜电位下的兴奋性保留和对重复刺激的反应可以通过已知的 Na(V)1.8 在 IB4+阳性神经元中的优先表达来解释,并且 IB4+阳性神经元在重复刺激时动作电流的减少支持了一种新的假说,即 Na(+)通道失活的积累可解释 C 纤维传导速度的减慢。

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