首页> 外文期刊>The Journal of Physiology >Excitability parameters and sensitivity to anemone toxin ATX-II in rat small diameter primary sensory neurones discriminated by Griffonia simplicifolia isolectin IB4.
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Excitability parameters and sensitivity to anemone toxin ATX-II in rat small diameter primary sensory neurones discriminated by Griffonia simplicifolia isolectin IB4.

机译:兴奋性参数和对海葵毒素ATX-II的大鼠小直径初级感觉神经元的敏感性由辛普森单叶叶isolectin IB4区分。

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摘要

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.
机译:感觉神经元亚型(<或= 25微米表观直径)表达各种Na(+)通道,其中表达与动作电位持续时间相关,并与差异性IB4-凝集素结合相关。我们假设对ATX-II的敏感性也可能区分神经元,并报告说1微米对IB4 + ve神经元的动作电位影响可忽略或很小,但在IB4 ve神经元中的动作电位持续时间显着增加。该毒素未对耐河豚毒素(TTX-r)的Na(V)1.8电流起作用。歧视是基于河豚毒素敏感(TTX-s)Na(+)通道表达。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 + ve和ve神经元中动作电流的影响。在100至20 mV范围内,IB4 + ve神经元在去极化时变得更具兴奋性,但是IB4 ve神经元在55 mV附近表现出峰值兴奋性,而在20 mV时则无兴奋性。在2 Hz时产生的动作电位升高,我们发现IB4 + ve神经元的内向动作电流峰值减小,而大多数IB4 ve神经元的电流幅度变化可忽略不计。我们的发现与相对毒素不敏感的通道(包括在IB4 + ve神经元中表达的Na(V)1.7)一致,而毒素敏感性表明IB4 ve神经元可能表达Na(V)1.1或Na(V)1.2,或两者都表达。在IB4 + ve神经元中Na(V)1.8的优先表达可以解释低膜电位下的兴奋性保留和对重复刺激的响应,而在重复刺激下IB4 + ve神经元中动作电流的减少支持了新颖的假说解释了Na(+)通道失活的积累导致C纤维中传导速度的减慢。

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