Sauviat M P, Ecault E, Faivre J F, Findlay I
Laboratoire de Physiologie Comparée (URA CNRS 1121), Orsay, France.
Pflugers Arch. 1991 Apr;418(3):261-5. doi: 10.1007/BF00370524.
To examine the effects of the activation of adenosine 5'-triphosphate (ATP)-sensitive K channels in a skeletal muscle we have applied the ATP-sensitive K channel opener SR44866 whilst recording single ion channels, voltage-clamped membrane currents, evoked action potentials and tension in sartorius muscles of the frog. In excised inside-out membrane patches SR44866 opened channels which could be inhibited by internal ATP and glibenclamide. In voltage-clamped individual muscle fibres SR44866 evoked a glibenclamide-sensitive membrane current which reversed at -70 mV. The effect of SR44866 was dose dependent with an effective concentration for 50% maximal effect (EC50) of 67 microM and a slope factor of 2. SR44866 dose dependently reduced the duration of the spike after-potential, spike overshoot, Vmax, tetrodotoxin-sensitive voltage-gated inward membrane currents and muscle twitch tension. From this evidence it can be concluded that the opening of ATP-sensitive K channels may be associated with the inhibition of contraction of skeletal muscle.
为了研究激活骨骼肌中三磷酸腺苷(ATP)敏感性钾通道的作用,我们在记录青蛙缝匠肌的单离子通道、电压钳制膜电流、诱发动作电位和张力的同时,应用了ATP敏感性钾通道开放剂SR44866。在切除的内向外膜片中,SR44866使通道开放,该通道可被胞内ATP和格列本脲抑制。在电压钳制的单个肌纤维中,SR44866诱发了一种对格列本脲敏感的膜电流,其反转电位为-70 mV。SR44866的作用呈剂量依赖性,最大效应的50%有效浓度(EC50)为67 μM,斜率因子为2。SR44866剂量依赖性地缩短了动作电位后电位的持续时间、动作电位超射、最大去极化速率、河豚毒素敏感的电压门控内向膜电流和肌肉抽搐张力。由此证据可以得出结论,ATP敏感性钾通道的开放可能与骨骼肌收缩的抑制有关。