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Effects of Dofetilide on Membrane Currents in Sinoatrial Node Cells of Rabbit

机译:多非利特对家兔窦房结细胞膜电流的影响

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References(12) Cited-By(4) The effects of dofetilide (UK 68798) on membrane currents were examined in isolated sinoatrial node cells of rabbits by using patch clamping. At a concentration of 1 pM, dofetilide decreased the delayed rectifier K+ current (IK) (50.2±10.2%, mean±S.E.). The Ca2+ current was slightly decreased during the application of dofetilide. However, the decrease in the current may be attributed to the “run down” phenomenon. The drug did not affect the hyperpolarization-activated inward current. Therefore, dofetilide exhibited class III antiarrhythmic activity in rabbit sinoatrial node cells. Similarly, E-4031 (1-[2-(6-methyl-2-pyridyl)ethyl]-4-(4-methylsulfonylaminobenzoyl)pireridine) (1 μM), a standard class III agent, also showed specific inhibition of IK. Furthermore, dofetilide depolarized the maximum diastolic potentials, reduced the slope of the pacemaker potential and then abolished spontaneously firing action potentials in the nodal cells. The results demonstrate that dofetilide may produce negative chronotropic effects as a result of its class III activity.
机译:参考文献(12)被引用的文献(4)使用膜片钳在兔离体窦房结细胞中检测了多非利特(UK 68798)对膜电流的影响。在1 pM的浓度下,多芬利特降低了延迟整流器K +电流(IK)(50.2±10.2%,平均值±标准误差)。在使用多芬替利期间,Ca2 +电流略有降低。但是,电流的减少可能归因于“耗尽”现象。该药物不影响超极化激活的内向电流。因此,多非利特在兔窦房结细胞中表现出III类抗心律不齐活性。类似地,标准的III类药物E-4031(1- [2-(6-甲基-2-吡啶基)乙基] -4-(4-甲基磺酰基氨基苯甲酰基)吡咯烷)(1μM)也显示出对IK的特异性抑制。此外,多非利特使最大舒张电位去极化,降低了起搏器电位的斜率,然后取消了节细胞中的自发放电动作电位。结果表明多非利特由于其III类活性而可能产生负面的变时作用。

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