Denton J S, Leiter J C
Department of Physiology, Dartmouth Medical School, Lebanon, NH 03756, USA.
J Membr Biol. 2002 Nov 1;190(1):17-28. doi: 10.1007/s00232-002-1021-9.
The model proposed for external TEA block of Shaker K+ channels predicts a proportional relationship between TEA sensitivity and calculated electrical distance derived from measurements of voltage dependence of TEA block. In the present study, we examined this relationship for the A-type K+ current (IA) of Helix aspersa in neuronal somata using the whole-cell patch-clamp technique. External TEA inhibited IA with strong voltage dependence, such that the TEA dissociation constant was increased at depolarized test potentials. The half-inhibition constant (V0.5) for TEA block was approximately 21 mM at 0 mV, and V0.5 increased to approximately 67 mM at 50 mV. The calculated electrical distance for TEA block suggested that TEA traversed 65% of the way into the membrane electrical field. TEA also caused significant shifts in the voltage-dependence of A-type K+ channel gating. For example, at TEA concentrations below that required to fully suppress delayed outward currents, TEA caused depolarizing shifts in the voltage-dependence of A-type channel activation, steady-state inactivation, time for removal of inactivation, and slowed channel activation kinetics. Taken together, these observations suggest that TEA biased the local field potential near voltage-sensing domains of A-type K+ channels, causing the transmembrane electrical field to be relatively hyperpolarized in the presence of TEA. In summary, the calculated electrical distance of TEA block of A-type K+ channels in H. aspersa neurons is unprecedented among other K+ channels. This raises concerns about the conventional interpretation of this value. Furthermore, the voltage-dependent properties of IA are modified by TEA at concentrations previously used to isolate delayed rectifier potassium channels (IKDR) selectively. This lack of specificity has important implications for recent, as well as future studies of IA in H. aspersa and possibly other snail neurons.
所提出的针对摇椅式钾通道的外部四乙铵(TEA)阻断模型预测,TEA敏感性与根据TEA阻断电压依赖性测量得出的计算电距离之间存在比例关系。在本研究中,我们使用全细胞膜片钳技术,在神经元胞体中研究了光滑琥珀螺的A型钾电流(IA)的这种关系。外部TEA以强烈的电压依赖性抑制IA,使得TEA解离常数在去极化测试电位时增加。TEA阻断的半抑制常数(V0.5)在0 mV时约为21 mM,在50 mV时增加到约67 mM。TEA阻断的计算电距离表明,TEA穿过了进入膜电场65%的路径。TEA还导致A型钾通道门控的电压依赖性发生显著变化。例如,在低于完全抑制延迟外向电流所需浓度的TEA浓度下,TEA导致A型通道激活、稳态失活、失活去除时间的电压依赖性发生去极化偏移,并减慢通道激活动力学。综上所述,这些观察结果表明,TEA使A型钾通道电压感应域附近的局部场电位发生偏移,导致在存在TEA的情况下跨膜电场相对超极化。总之,光滑琥珀螺神经元中A型钾通道的TEA阻断计算电距离在其他钾通道中是前所未有的。这引发了对该值传统解释的担忧。此外,在先前用于选择性分离延迟整流钾通道(IKDR)的浓度下,IA的电压依赖性特性会被TEA改变。这种缺乏特异性对光滑琥珀螺以及可能其他蜗牛神经元中IA的近期和未来研究具有重要意义。