Undrovinas A I, Iushmanova A V, Rozenshtraukh L V
Biull Eksp Biol Med. 1980 Aug;90(8):178-80.
The voltage clamp experiments were carried out on single internally perfused rat myocardial cells. The effect of ethmozine (8 x 10(-5) g/ml) and lidocain (8 x 10(-6) g/ml) on the fast maximum inward sodium current (INa) was studied. The drugs were tested inside and outside the cell. INa was inhibited insignificantly when ethmozine was added inside the cell. After 5 min of ethmozine action outside the cell INa dropped on the average to 43 +/- 6% of its initial value. Under these conditions the reactivation constrant of INa did not change significantly. Lidocain depressed INa both when added outside and inside the cell. However, when lidocain was added outside the cell a longer period was needed to depress INa. Comparison of lidocain and ethmozine action outside and inside the myocardial cell has shown that the sites of action of these antiarrhythmic drugs on the cellular membrane are different.
电压钳实验是在单个经内部灌注的大鼠心肌细胞上进行的。研究了乙莫嗪(8×10⁻⁵g/ml)和利多卡因(8×10⁻⁶g/ml)对快速最大内向钠电流(INa)的影响。这些药物在细胞内和细胞外都进行了测试。当在细胞内加入乙莫嗪时,INa受到的抑制不明显。在细胞外给予乙莫嗪作用5分钟后,INa平均降至其初始值的43±6%。在这些条件下,INa的再激活常数没有明显变化。利多卡因在细胞外和细胞内加入时均能抑制INa。然而,当在细胞外加入利多卡因时,抑制INa需要更长的时间。心肌细胞内外利多卡因和乙莫嗪作用的比较表明,这些抗心律失常药物在细胞膜上的作用位点不同。