Comtois A, Light P, Renaud J M
University of Ottawa, Department of Physiology, Ontario, Canada.
J Pharmacol Exp Ther. 1995 Sep;274(3):1061-6.
The goal of this study was to determine how blocking ATP-sensitive K+ channels with tolbutamide affects the excitability and contractility of intact frog sartorius muscle during fatigue development. Fatigue was elicited with one tetanic contraction every sec for 3 min. During fatigue the resting potential decreased by 10 mV although the action potential overshoot remained constant. The addition of 2 mmol.liter-1 tolbutamide 60 min before fatigue did not modify the effect of fatigue on the resting potential and action potential overshoot. During fatigue development the half-repolarization time of control muscles increased by 0.26 msec in control muscles, although it increased by 0.77 msec in the presence of 2 mmol.liter-1 tolbutamide; the difference was significant. The decrease in force during fatigue development was not affected by 2 mmol.liter-1 tolbutamide (added 60 min before fatigue), whereas the recovery of force after fatigue was slower in tolbutamide- exposed muscles than in control muscles. Addition of 2 mmol.liter-1 tolbutamide after 5 min of recovery reduced the recovery rate of the resting potential and half-repolarization time, but did not affect the recovery of tetanic force during the first 40 min. Our results are consistent with the hypothesis that ATP-sensitive K+ channels are activated during fatigue development and that they contribute to the repolarization phase of action potentials, but they do not support the hypothesis that ATP-sensitive K+ channels contribute to the decrease in force.
本研究的目的是确定用甲苯磺丁脲阻断ATP敏感性钾通道如何影响完整青蛙缝匠肌在疲劳发展过程中的兴奋性和收缩性。每隔1秒进行一次强直收缩,持续3分钟来诱发疲劳。在疲劳过程中,静息电位下降了10 mV,而动作电位的超射保持不变。在疲劳前60分钟添加2 mmol·L⁻¹甲苯磺丁脲并没有改变疲劳对静息电位和动作电位超射的影响。在疲劳发展过程中,对照肌肉的半复极化时间增加了0.26毫秒,而在存在2 mmol·L⁻¹甲苯磺丁脲的情况下增加了0.77毫秒;差异显著。疲劳发展过程中的力量下降不受2 mmol·L⁻¹甲苯磺丁脲(疲劳前60分钟添加)的影响,而在暴露于甲苯磺丁脲的肌肉中,疲劳后力量的恢复比对照肌肉慢。在恢复5分钟后添加2 mmol·L⁻¹甲苯磺丁脲降低了静息电位和半复极化时间的恢复率,但在前40分钟内不影响强直收缩力的恢复。我们的结果与以下假设一致:ATP敏感性钾通道在疲劳发展过程中被激活,并且它们有助于动作电位的复极化阶段,但它们不支持ATP敏感性钾通道导致力量下降的假设。