Takano M, Ashcroft F M
University Laboratory of Physiology, Oxford, UK.
Pflugers Arch. 1996 Feb;431(4):625-31. doi: 10.1007/BF02191912.
We studied the block of whole-cell ATP-sensitive K+ (KATP) currents in mouse pancreatic beta-cells produced by external Ba2+. Ba2+ produced a time-and voltage-dependent block of KATP currents, both the rate and extent of the block increasing with hyperpolarization. With 5.6 mM [K+]o, the relationship between the steady-state KATP current and [Ba2+]o was fit by the Hill equation with a Kd of 12.5 +/- 2.8 microM at -123 mV and of 0.18 +/- 0.02 mM at -62 mV. The Hill coefficient (n) was close to 1 at all potentials indicating that binding of a single Ba2+ ion is sufficient to block the channel. When [K+]o was raised to 28 mM the Kd was little changed (12.4 +/- 4.1 microM at -123 mV, 0.27 +/- 0.05 mM at -62 mV) and n was unaffected, suggesting that K+ does not interact with the Ba2+ binding site. The kinetics of Ba2+ block were slow, 10 microM Ba2+ blocking the KATP current with a time constant of 20 ms at -123 mV in 28 mM [K+]o. The blocking rate constant was calculated as 1.7 mM-1ms-1 and the unblocking rate as 0.02 ms-1, at -123 mV. The data are discussed in terms of a model in which Ba2+ binds to a site at the external mouth of the channel to inhibit the KATP channel.
我们研究了细胞外Ba2+对小鼠胰腺β细胞全细胞ATP敏感性钾通道(KATP)电流的阻断作用。Ba2+对KATP电流产生时间和电压依赖性阻断,阻断速率和程度均随超极化增加。在5.6 mM [K+]o条件下,稳态KATP电流与[Ba2+]o的关系符合Hill方程,在-123 mV时Kd为12.5±2.8 μM,在-62 mV时为0.18±0.02 mM。在所有电位下,Hill系数(n)均接近1,表明单个Ba2+离子的结合足以阻断通道。当[K+]o升高至28 mM时,Kd变化不大(在-123 mV时为12.4±4.1 μM,在-62 mV时为0.27±0.05 mM),n不受影响,提示K+不与Ba2+结合位点相互作用。Ba2+阻断的动力学较慢,在28 mM [K+]o条件下,10 μM Ba2+在-123 mV时以20 ms的时间常数阻断KATP电流。在-123 mV时,阻断速率常数计算为1.7 mM-1ms-1,解阻断速率为0.02 ms-1。根据Ba2+结合于通道外口位点以抑制KATP通道的模型对数据进行了讨论。