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Internal Na+ and Mg2+ blockade of DRK1 (Kv2.1) potassium channels expressed in Xenopus oocytes. Inward rectification of a delayed rectifier

机译:在非洲爪蟾卵母细胞中表达的DRK1(Kv2.1)钾通道的内部Na +和Mg2 +阻断。延迟整流器的内向整流

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摘要

Delayed rectifier potassium channels were expressed in the membrane of Xenopus oocytes by injection of rat brain DRK1 (Kv2.1) cRNA, and currents were measured in cell-attached and inside-out patch configurations. In intact cells the current-voltage relationship displayed inward going rectification at potentials > +100 mV. Rectification was abolished by excision of membrane patches into solutions containing no Mg2+ or Na+ ions, but was restored by introducing Mg2+ or Na+ ions into the bath solution. At +50 mV, half- maximum blocking concentrations for Mg2+ and Na+ were 4.8 +/- 2.5 mM (n = 6) and 26 +/- 4 mM (n = 3) respectively. Increasing extracellular potassium concentration reduced the degree of rectification of intact cells. It is concluded that inward going rectification resulting from voltage-dependent block by internal cations can be observed with normally outwardly rectifying DRK1 channels.
机译:通过注射大鼠脑DRK1(Kv2.1)cRNA,在非洲爪蟾卵母细胞膜中表达了延迟的整流钾通道,并在细胞附着和由内而外的贴片配置中测量了电流。在完整的电池中,电流-电压关系在电势> +100 mV时显示向内整流。通过将膜片切成不包含Mg2 +或Na +离子的溶液来取消整流,但是可以通过将Mg2 +或Na +离子引入浴液中来恢复。在+50 mV时,Mg2 +和Na +的半最大阻断浓度分别为4.8 +/- 2.5 mM(n = 6)和26 +/- 4 mM(n = 3)。增加细胞外钾浓度会降低完整细胞的整流程度。结论是,可以通过正常向外整流的DRK1通道观察到由内部阳离子引起的电压依赖性阻断导致的向内整流。

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  • 年度 1994
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