Division of Pharmacological Science, Department of Health Science, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
J Pharmacol Sci. 2010;114(1):111-4. doi: 10.1254/jphs.10066sc. Epub 2010 Aug 11.
We examined the effect of azimilide, a class III antiarrhythmic drug, on Na(+)/Ca(2+) exchange current (I(NCX)) in guinea-pig cardiac single ventricular cells. External application of azimilide suppressed bi-directional I(NCX) in a concentration-dependent manner. IC(50) values for outward and inward I(NCX) were 45 and 40 µM, respectively, with Hill coefficients of 1. Azimilide attenuated I(NCX) in the presence of trypsin in the patch pipette, indicating that azimilide is a trypsin-insensitive NCX inhibitor. Delayed afterdepolarization induced by electrical stimulation with ouabain disappeared in the presence of 30 µM azimilide. We conclude that azimilide inhibits NCX at supratherapeutic concentrations.
我们研究了 III 类抗心律失常药物决奈达隆对豚鼠心脏单个心室细胞钠钙交换电流(I(NCX))的影响。决奈达隆的外源性应用呈浓度依赖性抑制双向 I(NCX)。外向和内向 I(NCX)的 IC(50)值分别为 45 和 40 μM,Hill 系数均为 1。决奈达隆在膜片钳内的胶状小牛胰腺蛋白酶存在下可减弱 I(NCX),表明决奈达隆是一种不易受胶状小牛胰腺蛋白酶影响的 NCX 抑制剂。在 30 μM 决奈达隆存在的情况下,电刺激引起的延迟后除极消失。我们得出结论,在超治疗浓度下,决奈达隆抑制 NCX。