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Effects of intracellular magnesium on Kv1.5 and Kv2.1 potassium channels

机译:细胞内镁对Kv1.5和Kv2.1钾通道的影响

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We characterized the effects of intracellular Mg2+ (Mg2+ i) on potassium currents mediated by the Kv1.5 and Kv2.1 channels expressed in Xenopus oocytes. Increase in Mg2+ i caused a voltage-dependent block of the current amplitude, apparent acceleration of the current kinetics (explained by a corresponding shift in the steady-state activation) and leftward shifts in activation and inactivation dependencies for both channels. The voltage-dependent block was more potent for Kv2.1 [dissociation constant at 0 mV, K d(0), was ~70 mM and the electric distance of the Mg2+ binding site, δ, was 0.2] than for the Kv1.5 channel [K d(0)~40 mM and δ=0.1]. Similar shifts in the voltage-dependent parameters for both channels were described by the Gouy-Chapman formalism with the negative charge density of 1 e−/100 Å2. Additionally, Mg2+ i selectively reduced a non-inactivating current and increased the accumulation of inactivation of the Kv1.5, but not the Kv2.1 channel. A potential functional role of the differential effects of Mg2+ i on the Kv channels is discussed.
机译:我们表征了细胞内Mg2 + (Mg2 + i )对爪蟾卵母细胞表达的Kv1.5和Kv2.1通道介导的钾电流的影响。 Mg2 + i 的增加引起电流幅度的电压依赖块,电流动力学的明显加速(由稳态激活的相应位移来解释)以及激活和失活依赖性的向左位移对于两个渠道。电压依赖性阻滞剂对Kv2.1更有效[解离常数为0 mV,K d(sub)(0)为〜70 mM,Mg2 + 结合位点的电距离为δ。 Kv1.5频道[K d(0)〜40 mM和δ= 0.1]。 Gouy-Chapman形式主义用负电荷密度为1 e- / 100Å2描述了两个通道的电压相关参数的类似变化。此外,Mg2 + i 选择性地降低了非灭活电流并增加了Kv1.5灭活的积累,但没有增加Kv2.1通道的灭活。讨论了Mg2 + i 对Kv通道的微分作用的潜在功能。

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