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The influence of protons and zinc ions on the steady-state inactivation of Kv1.3 potassium channels

机译:质子和锌离子对Kv1.3钾通道稳态失活的影响

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Using the whole-cell patch-clamp technique, we investigated the influence of extracellular pH and zinc ions (Zn2+) on the steady-state inactivation of Kv1.3 channels expressed in human lymphocytes. The obtained data showed that lowering the extracellular pH from 7.35 to 6.8 shifted the inactivation midpoint (Vi) by 17.4 ± 1.12 mV (n = 6) towards positive membrane potentials. This shift was statistically significant (p 0.05). Applying 100 μM Zn2+ at pH 6.8 further shifted the Vi value by 16.55 ± 1.80 mV (n = 6) towards positive membrane potentials. This shift was also statistically significant (p 0.05). The total shift of the Vi by protons and Zn2+ was 33.95 ± 1.90 mV (n = 6), which was significantly higher (p 0.05) than the shift caused by Zn2+ alone. The Zn2+-induced shift of the Vi at pH 6.8 was almost identical to the shift at pH = 7.35. Thus, the proton-and Zn2+-induced shifts of the Vi value were additive. The steady-state inactivation curves as a function of membrane voltage were compared with the functions of the steady-state activation. The total shift of the steady-state inactivation was almost identical to the total shift of the steady-state activation (32.01 ± 2.10 mV, n = 10). As a result, the “windows” of membrane potentials in which the channels can be active under physiological conditions were also markedly shifted towards positive membrane potentials. The values of membrane voltage and the normalised chord conductance corresponding to the points of intersection of the curves of steady-state activation and inactivation were also calculated. The possible physiological significance of the observed modulatory effects is discussed herein.
机译:使用全细胞膜片钳技术,我们调查了细胞外pH和锌离子(Zn2 +)对人淋巴细胞中表达的Kv1.3通道稳态失活的影响。获得的数据表明,将细胞外pH从7.35降低至6.8,可使失活中点(Vi)朝着膜正电位移动17.4±1.12 mV(n = 6)。该变化具有统计学意义(p <0.05)。在pH 6.8下施加100μMZn2 +进一步使Vi值向膜正电位移动16.55±1.80 mV(n = 6)。此变化在统计学上也很显着(p <0.05)。通过质子和Zn2 +引起的Vi的总位移为33.95±1.90 mV(n = 6),比单独使用Zn2 +引起的位移明显更高(p <0.05)。 Zn2 +诱导的Vi在pH 6.8处的位移几乎与pH = 7.35时的位移相同。因此,质子和Zn 2+引起的Vi值的偏移是累加的。将稳态失活曲线作为膜电压的函数与稳态活化的函数进行比较。稳态失活的总位移与稳态活化的总位移几乎相同(32.01±2.10 mV,n = 10)。结果,其中通道可以在生理条件下起作用的膜电位的“窗口”也明显地移向正膜电位。还计算了与稳态活化和失活曲线的交点相对应的膜电压和归一化弦电导率的值。本文讨论了所观察到的调节作用的可能的生理学意义。

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