Lacampagne A, Caputo C, Argibay J
Laboratoire de Physiologie des Cellules Cardiaques et Vasculaires, Faculté des Sciences, Tours, France.
Biophys J. 1996 Jan;70(1):370-5. doi: 10.1016/S0006-3495(96)79580-2.
The effects of 100 microM ryanodine on the L-type calcium channel were studied using the pacth-clamp technique in isolated guinea pig ventricular myocytes. The inactivation kinetics of the calcium current were slowed down in the presence of ryanodine in agreement with the blockade of the release of calcium from the sarcoplasmic reticulum by the drug. The I-V and steady-state inactivation curves of the calcium current were shifted to negative values by ryanodine. A similar shift was observed in the activation and inactivation curves of the intramembrane charge movement associated with the calcium channel. Due to this shift, ryanodine slightly reduced the maximal amount of displaced charge although it did not modify the transition from the inactivated to the activated state (i.e., charge movement repriming). This result is in notable contrast with that obtained in skeletal muscle, where it has been found that ryanodine interferes with charge movement repriming. These results provide additional evidence of the postulated differences between the architecture of the excitation-contraction coupling system in cardiac and skeletal muscle.
利用膜片钳技术,在分离的豚鼠心室肌细胞中研究了100微摩尔的兰尼碱对L型钙通道的影响。在存在兰尼碱的情况下,钙电流的失活动力学减慢,这与该药物对肌浆网钙释放的阻断作用一致。兰尼碱使钙电流的I-V曲线和稳态失活曲线向负值偏移。在与钙通道相关的膜内电荷移动的激活和失活曲线中也观察到类似的偏移。由于这种偏移,兰尼碱略微降低了最大移位电荷量,尽管它没有改变从失活状态到激活状态的转变(即电荷移动再激活)。这一结果与在骨骼肌中获得的结果形成显著对比,在骨骼肌中发现兰尼碱会干扰电荷移动再激活。这些结果为心脏和骨骼肌兴奋-收缩偶联系统结构上的假定差异提供了额外证据。