Duan S, Cooke I M
Békésy Laboratory of Neurobiology and Department of Zoology, University of Hawaii, Honolulu, Hawaii 96822, USA.
J Neurophysiol. 1999 Apr;81(4):1848-55. doi: 10.1152/jn.1999.81.4.1848.
Although divalent cations and lanthides are well-known inhibitors of voltage-dependent Ca2+ currents (ICa), their ability to selectively inhibit a voltage-gated K+ current is less widely documented. We report that La3+ inhibits the transient K+ current (IA) of crab (Cardisoma carnifex) neurosecretory cells at ED50 approximately 5 microM, similar to that blocking ICa, without effecting the delayed rectifier K+ current (IK). Neurons were dissociated from the major crustacean neuroendocrine system, the X-organ-sinus gland, plated in defined medium, and recorded by whole cell patch clamp after 1-2 days in culture. The bath saline included 0.5 microM TTX and 0.5 mM CdCl2 to eliminate inward currents. Responses to depolarizing steps from a holding potential of -40 mV represented primarily IK. They were unchanged by La3+ up to 500 microM. Currents from -80 mV in the presence of 20 mM TEA were shown to represent primarily IA. La3+ (with TEA) reduced IA and maximum conductance (GA) by approximately 10% for 1 microM and another 10% each in 10 and 100 microM La3+. Normalized GA-V curves were well fit with a single Boltzmann function, with V1/2 +4 mV and slope 15 mV in control; V1/2 was successively approximately 15 mV depolarized and slope increased approximately 2 mV for each of these La3+ concentrations. Cd2+ (1 mM), Zn2+ (200 microM), and Pb2+ (100 microM) or removal of saline Mg2+ (26 mM) had little or no effect on IA. Steady-state inactivation showed similar right shifts (from V1/2 -39 mV) and slope increases (from 2.5 mV) in 10 and 100 microM La3+. Time to peak IA was slowed in 10 and 100 microM La3+, whereas curves of normalized time constants of initial decay from peak IA versus Vc were right-shifted successively approximately 15 mV for the three La3+ concentrations. The observations were fitted by a Woodhull-type model postulating a La3+-selective site that lies 0.26-0.34 of the distance across the membrane electric field, and both block of K+ movement and interaction with voltage-gating mechanisms; block can be relieved by depolarization and/or outward current. The observation of selective inhibition of IA by micromolar La3+ raises concerns about its use in studies of ICa to evaluate contamination by outward current.
尽管二价阳离子和镧系元素是众所周知的电压依赖性Ca2+电流(ICa)抑制剂,但其选择性抑制电压门控K+电流的能力却鲜有文献记载。我们报告称,La3+在ED50约为5 microM时抑制蟹(食蟹硬壳蟹)神经分泌细胞的瞬时K+电流(IA),这与阻断ICa的情况相似,而对延迟整流K+电流(IK)没有影响。神经元从主要的甲壳类神经内分泌系统X器官 - 窦腺中解离出来,接种在特定培养基中,培养1 - 2天后通过全细胞膜片钳记录。浴槽灌流液包含0.5 microM TTX和0.5 mM CdCl2以消除内向电流。从 - 40 mV的 holding 电位进行去极化步骤所引发的反应主要代表IK。在高达500 microM的La3+存在下,它们没有变化。在20 mM TEA存在的情况下,从 - 80 mV引发的电流主要代表IA。La3+(与TEA一起)在1 microM时使IA和最大电导(GA)降低约10%,在10 microM和100 microM La3+时又分别降低10%。归一化的GA - V曲线与单个玻尔兹曼函数拟合良好,对照组中V1/2为 + 4 mV,斜率为15 mV;对于这些La3+浓度中的每一个,V1/2依次大约去极化15 mV,斜率增加约2 mV。Cd2+(1 mM)、Zn2+(200 microM)和Pb2+(100 microM)或去除灌流液中的Mg2+(26 mM)对IA几乎没有影响。稳态失活在10 microM和100 microM La3+中显示出类似的右移(从V1/2 - 39 mV)和斜率增加(从2.5 mV)。在10 microM和100 microM La3+中,IA达到峰值的时间减慢,而从IA峰值开始的初始衰减的归一化时间常数曲线相对于Vc依次右移约15 mV,对应三种La3+浓度。这些观察结果通过Woodhull型模型进行拟合,该模型假设存在一个La3+选择性位点,其位于跨膜电场距离的0.26 - 0.34处,并且既存在对K+移动的阻断又存在与电压门控机制的相互作用;去极化和/或外向电流可解除这种阻断。微摩尔浓度的La3+对IA的选择性抑制这一观察结果引发了对其在ICa研究中用于评估外向电流污染情况的担忧。