Filippov A K, Bukeĭ T I, Kobrinskiĭ E M, Porotikov V I, Sakson M E
Biofizika. 1989 Jan-Feb;34(1):107-12.
It has been shown on the frog auricle fibres by the method of double sucrose bridge that the dependence of the effect of dihydropyridine Ca agonists BAYK 8644, CGP 28 392 and (-S)202 = 791 on calcium channels on the membrane potential is to a large extent due to the activation and following inactivation of Ca channels "silent" in the control. This effect takes place due to a shift by Ca agonists of the stationary curve of channel activation to hyperpolarization. The absence of stimulus-dependence of the agonist effect and constant time of Ca current reactivation suggest that the agonists bind with resting channels.
通过双蔗糖桥方法在蛙心耳纤维上已表明,二氢吡啶类钙激动剂BAYK 8644、CGP 28 392和(-S)202 = 791对钙通道的作用对膜电位的依赖性在很大程度上归因于对照中“沉默”的钙通道的激活及随后的失活。这种效应是由于钙激动剂使通道激活的稳态曲线向超极化方向移动而发生的。激动剂效应不存在刺激依赖性以及钙电流再激活时间恒定,这表明激动剂与静息通道结合。