Nakao M, Gadsby D C
Laboratory of Cardiac Physiology, Rockefeller University, New York, NY 10021.
J Gen Physiol. 1989 Sep;94(3):539-65. doi: 10.1085/jgp.94.3.539.
Na/K pump current was determined between -140 and +60 mV as steady-state, strophanthidin-sensitive, whole-cell current in guinea pig ventricular myocytes, voltage-clamped and internally dialyzed via wide-tipped pipettes. Solutions were designed to minimize all other components of membrane current. A device for exchanging the solution inside the pipette permitted investigation of Na/K pump current-voltage (I-V) relationships at several levels of pipette [Na] [( Na]pip) in a single cell; the effects of changes in external [Na] [( Na]o) or external [K] [( K]o) were also studied. At 50 mM [Na]pip, 5.4 mM [K]o, and approximately 150 mM [Na]o, Na/K pump current was steeply voltage dependent at negative potentials but was approximately constant at positive potentials. Under those conditions, reduction of [Na]o enhanced pump current at negative potentials but had little effect at positive potentials: at zero [Na]o, pump current was only weakly voltage dependent. At 5.4 mM [K]o and approximately 150 mM [Na]o, reduction of [Na]pip from 50 mM scaled down the sigmoid pump I-V relationship and shifted it slightly to the right (toward more positive potentials). Pump current at 0 mV was activated by [Na]pip according to the Hill equation with best-fit K0.5 approximately equal to 11 mM and Hill coefficient nH approximately equal to 1.4. At zero [Na]o, reduction of [Na]pip seemed to simply scale down the relatively flat pump I-V relationship: Hill fit parameters for pump activation by [Na]pip at 0 mV were K0.5 approximately equal to 10 mM, nH approximately equal to 1.4. At 50 mM [Na]pip and high [Na]o, reduction of [K]o from 5.4 mM scaled down the sigmoid I-V relationship and shifted it slightly to the right: at 0 mV, K0.5 approximately equal to 1.5 mM and nH approximately equal to 1.0. At zero [Na]o, lowering [K]o simply scaled down the flat pump I-V relationships yielding, at 0 mV, K0.5 approximately equal to 0.2 mM, nH approximately equal to 1.1. The voltage-independent activation of Na/K pump current by both intracellular Na ions and extracellular K ions, at zero [Na]o, suggests that neither ion binds within the membrane field. Extracellular Na ions, however, seem to have both a voltage-dependent and a voltage-independent influence on the Na/K pump: they inhibit outward Na/K pump current in a strongly voltage-dependent fashion, with higher apparent affinity at more negative potentials (K0.5 approximately equal to 90 mM at -120 mV, and approximately 170 mM at -80 mV), and they compete with extracellular K ions in a seemingly voltage-independent manner.(ABSTRACT TRUNCATED AT 400 WORDS)
钠钾泵电流是在-140至+60 mV之间测定的,作为豚鼠心室肌细胞中的稳态、毒毛花苷敏感的全细胞电流,通过宽口移液管进行电压钳制和细胞内透析。设计的溶液可使膜电流的所有其他成分降至最低。一种用于更换移液管内溶液的装置,可在单个细胞中研究几种移液管[Na]浓度([Na]pip)水平下的钠钾泵电流-电压(I-V)关系;还研究了外部[Na]([Na]o)或外部[K]([K]o)变化的影响。在50 mM [Na]pip、5.4 mM [K]o和约150 mM [Na]o条件下,钠钾泵电流在负电位时强烈依赖电压,但在正电位时大致恒定。在这些条件下,降低[Na]o可增强负电位时的泵电流,但对正电位影响很小:在[Na]o为零时,泵电流仅微弱依赖电压。在5.4 mM [K]o和约150 mM [Na]o条件下,将[Na]pip从50 mM降低会使S形泵I-V关系缩小,并使其略微向右移动(向更正的电位)。根据希尔方程,0 mV时的泵电流由[Na]pip激活,最佳拟合K0.5约等于11 mM,希尔系数nH约等于1.4。在[Na]o为零时,降低[Na]pip似乎只是简单地缩小了相对平坦的泵I-V关系:0 mV时由[Na]pip激活泵的希尔拟合参数为K0.5约等于10 mM,nH约等于1.4。在50 mM [Na]pip和高[Na]o条件下,将[K]o从5.4 mM降低会使S形I-V关系缩小并使其略微向右移动:在0 mV时,K0.5约等于1.5 mM,nH约等于1.0。在[Na]o为零时,降低[K]o只是简单地缩小了平坦的泵I-V关系,在0 mV时,K0.5约等于0.2 mM,nH约等于1.1。在[Na]o为零时,细胞内钠离子和细胞外钾离子对钠钾泵电流的电压非依赖性激活表明,这两种离子都不在膜电场内结合。然而,细胞外钠离子似乎对钠钾泵既有电压依赖性影响,也有电压非依赖性影响:它们以强烈的电压依赖性方式抑制外向钠钾泵电流,在更负的电位下具有更高的表观亲和力(-120 mV时K0.5约等于90 mM,-80 mV时约等于170 mM);并且它们以看似电压非依赖性的方式与细胞外钾离子竞争。(摘要截断于400字)