Nathan R D, Kanai K, Clark R B, Giles W
Department of Physiology and Biophysics, University of Texas Medical Branch, Galveston 77550.
J Gen Physiol. 1988 Apr;91(4):549-72. doi: 10.1085/jgp.91.4.549.
A single suction microelectrode voltage-clamp technique was used to study the actions of lanthanum ions (La3+) on ionic currents in single cells isolated from bullfrog right atrium. La3+, added as LaCl3, blocked the "slow" inward Ca2+ current (ICa) in a dose-dependent fashion; 10(-5) M produced complete inhibition. This effect was best fitted by a dose-response curve that was calculated assuming 1:1 binding of La3+ to a site having a dissociation constant of 7.5 x 10(-7) M. La3+ block was reversed (to 90% of control ICa) following washout and, in the presence of 10(-5) M La3+, was antagonized by raising the Ca2+ concentration from 2.5 to 7.5 mM (ICa recovered to 56% of the control). However, the latter effect took approximately 1 h to develop. Concentrations of La3+ that reduced ICa by 12-67%, 0.1-1.5 x 10(-6) M, had no measurable effect upon the voltage dependence of steady state ICa inactivation, which suggest that at these concentrations there are no significant surface-charge effects of La3+ on this gating mechanism. Three additional findings indicate that doses of La3+ that blocked ICa failed to produce nonspecific effects: (a) 10(-5) M La3+ had no measurable effect on the time-independent inwardly rectifying current, IK1; (b) the same concentration had no effect on the kinetics, amplitude, or voltage dependence of a time- and voltage-dependent K+ current, IK; and (c) 10(-4) M La3+ did not alter the size of the tetrodotoxin-sensitive inward Na+ current, INa, or the voltage dependence of its steady state inactivation. Higher concentrations (0.5-1.0 mM) reduced both IK1 and IK, and shifted the steady state activation curve for IK toward more positive potentials, presumably by reducing the external surface potential. Our results suggest that at a concentration of less than or equal to 10(-5) M, La3+ inhibits ICa selectively by direct blockade of Ca channels rather than by altering the external surface potential. At higher concentrations, La3+ exhibits nonspecific effects, including neutralization of negative external surface charge and inhibition of other time- and voltage-dependent ionic currents.
采用单吸力微电极电压钳技术研究镧离子(La3+)对从牛蛙右心房分离的单个细胞离子电流的作用。以LaCl3形式添加的La3+以剂量依赖性方式阻断“缓慢”内向Ca2+电流(ICa);10(-5) M可产生完全抑制。这种效应最适合通过剂量反应曲线来拟合,该曲线是在假设La3+与解离常数为7.5×10(-7) M的位点以1:1结合的情况下计算得出的。洗脱后La3+阻断作用被逆转(恢复到对照ICa的90%),并且在存在10(-5) M La3+的情况下,通过将Ca2+浓度从2.5 mM提高到7.5 mM可拮抗La3+的作用(ICa恢复到对照的56%)。然而,后一种效应大约需要1小时才能显现。使ICa降低12 - 67%的La3+浓度,即0.1 - 1.5×10(-6) M,对稳态ICa失活的电压依赖性没有可测量的影响,这表明在这些浓度下La3+对这种门控机制没有明显的表面电荷效应。另外三个发现表明,阻断ICa的La3+剂量未产生非特异性效应:(a)10(-5) M La3+对时间无关的内向整流电流IK1没有可测量的影响;(b)相同浓度对时间和电压依赖性K+电流IK的动力学、幅度或电压依赖性没有影响;(c)10(-4) M La3+没有改变河豚毒素敏感的内向Na+电流INa的大小或其稳态失活的电压依赖性。更高浓度(0.5 - 1.0 mM)降低了IK1和IK,并使IK的稳态激活曲线向更正的电位移动,可能是通过降低外表面电位。我们的结果表明,在浓度小于或等于10(-5) M时,La3+通过直接阻断Ca通道选择性抑制ICa,而不是通过改变外表面电位。在更高浓度下,La3+表现出非特异性效应,包括中和负性外表面电荷以及抑制其他时间和电压依赖性离子电流。