Thornbury K D, Ward S M, Sanders K M
Department of Physiology, University of Nevada School of Medicine, Reno 89557.
Am J Physiol. 1992 Jul;263(1 Pt 1):C226-36. doi: 10.1152/ajpcell.1992.263.1.C226.
The plateau phase of electrical slow waves in phasic gastrointestinal muscles is critical for excitation-contraction coupling. The plateau appears to depend upon a balance between inward Ca2+ current and outward K+ currents that is sustained for several seconds. Voltage-dependent, non-Ca(2+)-dependent K currents were studied in canine colonic circular muscle cells using the whole cell patch-clamp technique. At room temperature, depolarization activated a slow outward current that showed little inactivation during 500 ms. Increasing the temperature to 37 degrees C significantly increased the rate of activation of voltage-dependent outward current. The onset of the outward current overlapped the transient inward Ca2+ current, suggesting that this K current may act as a brake on the upstroke depolarization of electrical slow waves in intact muscles. Voltage-dependent outward current was sustained for the duration of test pulses. This current balanced the sustained inward current that was also activated at physiological test potentials. The outward current evoked by test pulses positive to -20 mV inactivated by at least 50% within 500 ms. Half inactivation occurred at -36 mV. Voltage-dependent K current was reduced by 4-aminopyridine (4-AP; 1-5 mM), but difference currents obtained by subtracting currents elicited from holding potentials of -45 mV from currents obtained from holding potentials of -100 mV were not affected by 4-AP (1 mM). Studies were also performed on intact muscles to test the effects of 4-AP on electrical slow waves. 4-AP increased the amplitude and rate of rise of the upstroke potential and increased the amplitude and prolonged the plateau phase of slow waves. These data suggest that a rapidly activating, inactivating, voltage-dependent K current participates in electrical slow waves of colonic circular smooth muscles.
阶段性胃肠肌电慢波的平台期对于兴奋-收缩偶联至关重要。该平台期似乎取决于内向Ca2+电流和外向K+电流之间的平衡,这种平衡可持续数秒。使用全细胞膜片钳技术在犬结肠环行肌细胞中研究了电压依赖性、非Ca(2+)依赖性K电流。在室温下,去极化激活了一种缓慢的外向电流,该电流在500毫秒内几乎没有失活。将温度升高到37摄氏度显著增加了电压依赖性外向电流的激活速率。外向电流的起始与瞬时内向Ca2+电流重叠,表明这种K电流可能在完整肌肉中作为电慢波上升期去极化的制动器。电压依赖性外向电流在测试脉冲期间持续存在。该电流平衡了在生理测试电位下也被激活的持续内向电流。测试脉冲在-20 mV以上诱发的外向电流在500毫秒内至少失活50%。半失活发生在-36 mV。电压依赖性K电流被4-氨基吡啶(4-AP;1-5 mM)降低,但通过从-100 mV的钳制电位获得的电流中减去从-45 mV的钳制电位获得的电流所得到的差异电流不受4-AP(1 mM)影响。还对完整肌肉进行了研究以测试4-AP对电慢波的影响。4-AP增加了上升期电位的幅度和上升速率,并增加了慢波的幅度并延长了平台期。这些数据表明,一种快速激活、失活的电压依赖性K电流参与结肠环行平滑肌的电慢波。