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Calcium and delayed potassium currents in mouse pancreatic beta-cells under voltage-clamp conditions.

机译:在电压钳制条件下,小鼠胰腺β细胞中的钙和钾延迟电流。

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摘要

Pancreatic islets of NMRI mice were dissociated into single cells which were kept in tissue culture for 1-3 days. The whole-cell configuration of the patch-clamp technique was used to study inward and delayed outward currents of beta-cells under voltage-clamp conditions at 20-22 degrees C. Outward currents were suppressed by substituting the impermeant cation N-methyl-D-glucamine for intracellular K+. The remaining inward current had a V-shaped current-voltage relation reaching a peak value of 39 +/- 4 pA (mean +/- S.E. of mean) around -15 mV. It was identified as a Ca2+ current, because the peak amplitude was increased 1.6 times by increasing external [Ca2+] ([Ca2+]o) from 2.6 mM to 10 mM and it was blocked by Co2+ (5 mM) or nifedipine (5 microM) but not by TTX (20 microM). The activation time constant of the inward current at -10 mV was 1.28 +/- 0.08 ms. The relation between the degree of activation (estimated from the size of the tail currents) and membrane potential V followed the sigmoidal function f = 1/(1 + exp [(Vh-V)/k]) with half-maximal activation potential, Vh = 4 +/- 1 mV and slope factor, k = 14 +/- 1 mV (for [Ca2+]o 10 mM). The inward current inactivated only weakly during depolarizing pulses of 0.1-1 s duration. The delayed outward current (in experiments with 155 mM-internal [K+] ([K+]i)) had a linear voltage dependence at potentials above -20 mV; its amplitude at -10 mV was 210 +/- 30 pA. Tail currents related to the activation of the outward current had K+-dependent reversal potentials. The current was blocked by extracellularly applied tetraethylammonium (20 mM) and 4-aminopyridine (2 mM). It was not affected by glibenclamide (3 microM), tolbutamide (0.2 mM) and alterations of intracellular [Ca2+] (1 nM-1 microM). The activation time constant of the outward current at -10 mV was 21 +/- 3 ms. The voltage dependence of activation could be described by the sigmoidal function (see above) with Vh = 19 +/- 1 mV and k = 5.6 +/- 0.4 mV. The outward current inactivated during long (15 s) depolarizing pre-pulses (time constant at -10 mV: 2.6 +/- 0.6 s). 50% inactivation occurred at Vh = -36 +/- 2 mV, k was -4.1 +/- 0.2 mV. Inward and outward currents during depolarizing voltage pulses in beta-cells are similar to Ca2+ and delayed K+ currents in other cell types. These currents seem sufficient to generate the action potentials of the beta-cell.
机译:将NMRI小鼠的胰岛分离为单个细胞,将其在组织培养物中保留1-3天。膜片钳技术的全细胞配置用于研究在20-22摄氏度的电压钳制条件下β细胞的内向和延迟外向电流。通过取代抗渗阳离子N-甲基-D抑制外向电流-葡萄糖胺用于细胞内K +。其余的流入电流具有V型电流-电压关系,在-15 mV附近达到39 +/- 4 pA的峰值(平均值的+/- +/- S.E.)。由于外部[Ca2 +]([Ca2 +] o)从2.6 mM增加到10 mM,峰值幅度增加了1.6倍,并且被Co2 +(5 mM)或硝苯地平(5 microM)阻止,因此将其识别为Ca2 +电流。但不是通过TTX(20 microM)。 -10 mV时内向电流的激活时间常数为1.28 +/- 0.08 ms。激活程度(根据尾电流的大小估算)与膜电位V之间的关系遵循S型曲线函数f = 1 /(1 + exp [(Vh-V)/ k]),其中激活电位为一半, Vh = 4 +/- 1 mV和斜率系数,k = 14 +/- 1 mV(对于[Ca2 +] o 10 mM)。进入电流仅在0.1-1 s持续时间的去极化脉冲期间微弱地失活。延迟的向外电流(在155 mM内部[K +]([K +] i)的实验中)在高于-20 mV的电势下具有线性电压依赖性;其在-10 mV时的振幅为210 +/- 30 pA。与向外电流激活相关的尾电流具有依赖于K +的逆转电位。电流被细胞外施加的四乙铵(20 mM)和4-氨基吡啶(2 mM)阻止。它不受格列本脲(3 microM),甲苯磺丁酰胺(0.2 mM)和细胞内[Ca2 +](1 nM-1 microM)改变的影响。 -10 mV时向外电流的激活时间常数为21 +/- 3 ms。激活的电压依赖性可以通过S形函数(见上文)描述,其中Vh = 19 +/- 1 mV,k = 5.6 +/- 0.4 mV。长时间(15 s)的去极化预脉冲(-10 mV时的时间常数:2.6 +/- 0.6 s)使向外的电流失活。在Vh = -36 +/- 2 mV时发生了50%的失活,k为-4.1 +/- 0.2 mV。 β细胞中去极化电压脉冲期间的内向和外向电流类似于其他细胞类型中的Ca2 +和延迟K +电流。这些电流似乎足以产生β细胞的动作电位。

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    Rorsman, P; Trube, G;

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  • 年度 1986
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