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Arsenazo III transients and calcium current in a normally non-spiking neuronal soma of crayfish.

机译:小龙虾正常无突触神经元体中的Arsenazo III瞬态和钙电流。

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摘要

Arsenazo III was used to investigate Ca2+ transients in the normally non-excitable soma of the motor giant neurones of the crayfish Procambarus clarkii. Two kinds of regenerative potentials could be obtained depending on membrane potential conditioning: a fast spike after a pre-hyperpolarization to -90 mV and a slow action potential after a pre-depolarization to -50 mV. Only the second of these was accompanied by an Arsenazo III transient. In voltage-clamped, somata injected, with tetraethylammonium chloride, an absorbance change could be obtained by pulsing the membrane potential above -44 mV. The relationship between absorbance change and potential peaked between 0 and +10 mV then fell off to zero at ca. +150 mV. Changes in light absorbance studied using double-pulse protocols suggested that the inactivation of Ca2+ entry was predominantly mediated by the intracellular free Ca2+ concentration. External application of 1 mM-CdCl2 abolished both the absorbance changes and the (Ca2+) inward current. The voltage dependence of this current was similar to that of the absorbance change. For positive membrane potential the current-voltage relationship showed a voltage-dependent conductance property, the origin of which is discussed.
机译:Arsenazo III用于研究小龙虾Procambarus clarkii运动巨神经元正常非兴奋性体中的Ca2 +瞬变。根据膜电位的调节,可以获得两种再生电位:超极化前至-90 mV后的快速尖峰和去极化前至-50 mV后的慢的动作电位。其中只有第二个伴随着Arsenazo III瞬态。在用四乙基氯化铵注入电压钳制的体细胞中,通过将膜电位脉冲至-44 mV以上可以获得吸光度的变化。吸光度变化和电势之间的关系在0至+10 mV之间达到峰值,然后在大约0下降至零。 +150毫伏。使用双脉冲协议研究的吸光度变化表明,Ca2 +进入的失活主要是由细胞内游离Ca2 +浓度介导的。外部施加1 mM-CdCl2消除了吸光度变化和(Ca2 +)内向电流。该电流的电压依赖性类似于吸光度变化。对于正膜电位,电流-电压关系显示出电压依赖性电导特性,并讨论了其起源。

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