The effects of tetraethylammonium (TEA) and 4-aminopyridine (4-AP) on membrane currents and on single channel K currents in smooth muscle cells isolated from canine trachea were examined by use of tight seal whole cell- and patch-clamp techniques. 2. Depolarizing current applied through a recording pipette did not elicit an action potential under current clamp. A strong outward rectification was observed. 3. In most cells under voltage-clamp, only an outward current was observed upon depolarization from -60 mV when a pipette solution contained mainly KCl. The outward current consisted of three components; a large initial transient, a following sustained component and an additional component of irregular small transients on the sustained one. The two transient components were almost abolished when extracellular and pipette solutions contained 2.2 mM Cd2+ (0 mM Ca2+) and 10 mM EGTA, respectively. The sustained component was well maintained under these conditions. 4. TEA at low concentrations (less than 1 mM) effectively decreased the transient components and made the outward current smooth; it also suppressed the sustained component at higher concentrations. In outside-out patches, external 1 mM TEA reduced the single channel conductance of Ca-activated K channels by about 87% whereas 3 mM 4-AP did not. 4-AP at low concentrations (less than 3 mM) selectively reduced the sustained component of the outward current. 5. A Ca current recorded after the suppression of outward current by internal Cs+ had a peak of approximately 200 pA at +10 mV (holding potential: -60 mV). The half inactivation voltage in the steady-state was approximately -30 mV. 6. Simultaneous application of 1 mM TEA and 4-AP reduced the outward current and unmasked a Ca current. Under these conditions, an action potential with overshoot was easily elicited under current clamp. 7. It is concluded that the low excitability of canine tracheal smooth muscle cell upon depolarization is due to a large outward K current which consists of Ca-dependent and Ca-independent components. The peak amplitude of the Ca current is similar to that in highly excitable smooth muscle cells such as those of the ureter.
摘要
运用紧密封接全细胞和膜片钳技术,研究了四乙铵(TEA)和4-氨基吡啶(4-AP)对从犬气管分离的平滑肌细胞膜电流和单通道钾电流的影响。2. 在电流钳制下,通过记录微电极施加的去极化电流未引发动作电位。观察到强烈的外向整流。3. 在电压钳制下的大多数细胞中,当微电极溶液主要含有KCl时,从-60 mV去极化时仅观察到外向电流。外向电流由三个成分组成;一个大的初始瞬变、一个随后的持续成分以及持续成分上不规则小瞬变的附加成分。当细胞外溶液和微电极溶液分别含有2.2 mM Cd2+(0 mM Ca2+)和10 mM乙二醇双四乙酸(EGTA)时,两个瞬变成分几乎完全消失。在这些条件下,持续成分得到很好的维持。4. 低浓度(小于1 mM)的TEA有效降低瞬变成分并使外向电流变得平滑;在较高浓度时它也抑制持续成分。在外侧向外膜片上,外部1 mM TEA使钙激活钾通道的单通道电导降低约87%,而3 mM 4-AP则没有。低浓度(小于3 mM)的4-AP选择性降低外向电流的持续成分。5. 在用内部Cs+抑制外向电流后记录的钙电流,在+10 mV(钳制电位:-60 mV)时峰值约为200 pA。稳态下的半失活电压约为-30 mV。6. 同时施加1 mM TEA和4-AP可降低外向电流并暴露出钙电流。在这些条件下,在电流钳制下容易引发超射动作电位。7. 得出结论,犬气管平滑肌细胞去极化时兴奋性低是由于大的外向钾电流,该电流由钙依赖性和钙非依赖性成分组成。钙电流的峰值幅度与输尿管等高度兴奋性平滑肌细胞中的相似。