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Inwardly rectifying, voltage-dependent and resting potassium currents in rat pancreatic acinar cells in primary culture.

机译:初级培养中大鼠胰腺腺泡细胞的内向整流,电压依赖性和静息钾电流。

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摘要

1. In exocrine pancreatic acinar cells in primary culture an inwardly rectifying, a voltage-dependent and a permanent resting K+ current were characterized. 2. Inwardly rectifying K+ currents could be elicited by elevation of the extracellular K+ concentration. The K+ inward currents were almost completely blocked by 5 mM Ba2+, whereas 10 mM TEA+ had only a partial effect. 3. Depolarizing voltage steps from negative clamp potentials evoked transient activation of a voltage-dependent K+ current. This voltage-dependent current could be blocked by 10 mM TEA+ and 1 mM 4-aminopyridine, but not by 5 mM Ba2+. 4. Neither the K+ inward rectifier nor the voltage-dependent K+ conductance produced a significant negative cell potential. Stable membrane potentials (-38.7 +/- 2.3 mV, n = 38) could only be recorded on cell clusters (> or = 5 cells). 5. Cell clusters, in contrast to single cells, had a permanent resting K+ conductance in addition to the inward rectifier and the voltage-dependent current. This resting K+ conductance was not blocked by TEA+, Ba2+, 4-aminopyridine or by the chromanol 293B. 6. Cytosolic alkalization by addition of NH4Cl to the bath solution decreased the resting K+ current. In parallel, electrical uncoupling of the cells and breakdown of the resting potential could be observed. The same effects could be produced when the cells were uncoupled by 0.2-1.0 mM n-octanol. It can be concluded that cell coupling is essential for maintenance of stable resting membrane potentials in pancreatic acinar cells.
机译:1.在原代培养的外分泌胰腺腺泡细胞中,特征在于向内整流,电压依赖性和永久性静息K +电流。 2.通过提高细胞外K +浓度可引起向内整流K +电流。 K +内向电流几乎完全被5 mM Ba2 +阻挡,而10 mM TEA +仅具有部分作用。 3.从负钳位电势开始对电压去极化,从而引起电压依赖性K +电流的瞬态激活。该电压依赖性电流可以被10 mM TEA +和1 mM 4-氨基吡啶阻止,但不能被5 mM Ba2 +阻止。 4. K +向内整流器和电压依赖性K +电导都不会产生明显的负电池电位。只能在细胞簇(>或= 5个细胞)上记录稳定的膜电位(-38.7 +/- 2.3 mV,n = 38)。 5.与单个电池相比,除了向内整流器和电压相关电流外,电池组还具有永久性的静息K +电导。 TEA +,Ba2 +,4-氨基吡啶或苯并二氢邻苯二甲酚293B不会阻止这种静止的K +电导。 6.通过向浴液中添加NH4Cl进行胞质碱化,可降低静止K +电流。同时,可以观察到细胞的电解偶联和静息电位的破坏。当细胞通过0.2-1.0 mM正辛醇解偶联时,可以产生相同的效果。可以得出结论,细胞偶联对于维持胰腺腺泡细胞中稳定的静止膜电位至关重要。

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