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电压钳制下的花园蜗牛神经元中的钾离子激活:一种由钙内流介导的成分。

Potassium activation in Helix aspersa neurones under voltage clamp: a component mediated by calcium influx.

作者信息

Meech R W, Standen N B

出版信息

J Physiol. 1975 Jul;249(2):211-39. doi: 10.1113/jphysiol.1975.sp011012.

Abstract
  1. Helix aspersa neurones under voltage clamp generate prolonged outward currents (potassium currents) in response to depolarizing command pulses. 2. The potassium currents recorded from cell A were reversibly reduced 25-50% by 10 mM cobalt ions in the bathing medium; 1 mM lanthanum, 10(-6) g/ml. D-600 and 10(-6) g/ml. iproveratril had similar effects but were only partially reversible. 3. The relationship between the potassium currents and the membrane potential had an "n" shape in normal saline. In calcium-free saline (containing 25 mM magnesium) the potassium currents were reduced and the "n" shape was abolished. The effect of calcium-free saline was readily reversible. 4. The voltage-dependence of the calcium-sensitive potassium currents was similar to that of the "late" calcium channel in squid axons (Baker, Hodgkin & Ridgway, 1971). 5. When cell A was depolarents were made up of two exponentially declining components. The slower of the two components was reduced in calcium-free saline. 6. When cell A was depolarized by 150 mV for 10 msec and then repolarized the "tail" currents were made up of a single rapidly declining component. The reversal potential of this component changed by 58 mV for a tenfold change in the external potassium concentration as predicted by the Nernst equation. 7. The reversal potential of "tail" currents having both components was less sensitive to changes in the external potassium concentration. 8. Tetraethylammonium (TEA) ions blocked both calcium dependent and voltage sensitive potassium currents. Each receptor was found to bind a single molecule of TEA. The dissociaton constant was about 10 mM in each case. 9. The intracellular concentration of ionized calcium was estimated from the potential at which there was no apparent calcium influx (the null point). It was between 3 x 10(-8) M and 8 x 10(-8) M with 10(-2) M calcium in the bathing medium. 10. The null point changed 30 mV for a tenfold change in the external calcium concentration as predicted by the Nernst equation. 11. It is concluded that depolarization of Helix neurones activates two typesof potassium channel. One channel is voltage dependent and highly selective for potassium. Activation of the other channel is dependent on the influx (or injection, see Meech, 1972, 1974a) of calcium. This calcium mediated potassium activation system saturates at high external calcium concentrations and is inhibited by external magnesium ions.
摘要
  1. 在电压钳制下,皱足蛞蝓神经元对去极化指令脉冲产生持续的外向电流(钾电流)。2. 从细胞A记录到的钾电流,在灌流介质中加入10 mM钴离子后可逆地降低了25 - 50%;1 mM镧、10⁻⁶ g/ml D - 600和10⁻⁶ g/ml维拉帕米有类似作用,但只是部分可逆。3. 在生理盐水中,钾电流与膜电位的关系呈“n”形。在无钙生理盐水(含25 mM镁)中,钾电流降低,“n”形消失。无钙生理盐水的作用很容易逆转。4. 钙敏感钾电流的电压依赖性与枪乌贼轴突中“晚期”钙通道的相似(贝克、霍奇金和里奇韦,1971年)。5. 当细胞A去极化时,电流由两个指数衰减成分组成。两个成分中较慢的那个在无钙生理盐水中降低。6. 当细胞A去极化150 mV持续10毫秒然后再复极化时,“尾电流”由一个单一的快速衰减成分组成。如能斯特方程所预测,外部钾浓度变化10倍时,该成分的逆转电位变化58 mV。7. 具有两个成分的“尾电流”的逆转电位对外部钾浓度变化较不敏感。8. 四乙铵(TEA)离子阻断钙依赖性和电压敏感性钾电流。发现每个受体结合一个TEA分子。每种情况下解离常数约为10 mM。9. 根据无明显钙内流时的电位(零点)估计细胞内游离钙浓度。灌流介质中有10⁻² M钙时,其浓度在3×10⁻⁸ M至8×10⁻⁸ M之间。10. 如能斯特方程所预测,外部钙浓度变化10倍时,零点变化30 mV。11. 得出结论,皱足蛞蝓神经元去极化激活两种类型的钾通道。一种通道是电压依赖性的,对钾具有高度选择性。另一种通道的激活依赖于钙的内流(或注入,见米奇,1972年,1974a)。这种钙介导的钾激活系统在高外部钙浓度下饱和,并被外部镁离子抑制。

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