Terrar Derek A, Wilson C M, Graham S G, Bryant S M, Heath B M
University Department of Pharmacology, Mansfield Road, Oxford, OX1 3QT, United Kingdom.
J Pharmacol Toxicol Methods. 2007 Sep-Oct;56(2):171-85. doi: 10.1016/j.vascn.2007.04.005. Epub 2007 May 26.
QT interval prolongation and Torsade de Pointes (TdP) arrhythmias are recognised as a potential risk with many drugs, most of which delay cardiac repolarization by inhibiting the rapidly activating K(+) current (I(Kr)). The objective of this study was to compare the effects of compounds on cardiac action potentials recorded from guinea-pig ventricular myocytes and dog Purkinje fibres.
Effects of dofetilide, sotalol, cisapride, terfenadine, haloperidol and sparfloxacin, compounds known to cause QT prolongation (positive controls), and nifedipine and verapamil, not associated with QT prolongation (negative controls) were studied on intracellular action potentials recorded from guinea-pig isolated ventricular myocytes (VM) and dog isolated Purkinje fibres (PF). Prolongation of action potential duration (APD) by sotalol, dofetilide and sparfloxacin was concentration-dependent and of greater magnitude in dog PF compared to guinea-pig VM. The maximum prolongation of APD in guinea-pig VM at 0.5 and 1 Hz was approximately 25% and this was associated with complete inhibition of I(Kr) by dofetilide. Effects on APD of cisapride and haloperidol in both preparations, and terfenadine in guinea-pig VM, were biphasic, consistent with inhibition of multiple ion channels. There was no effect of terfenadine on APD in dog PF. Haloperidol increased APD by more than 25% in guinea-pig VM, consistent with effects on additional repolarizing currents. The negative controls shortened APD to a greater extent in guinea-pig VM compared to dog PF. In general, the positive control drugs increased action potential triangulation (APD(40-90)) to a greater extent than APD(90).
Guinea-pig isolated VM may be more sensitive for detecting APD prolongation with compounds inhibiting multiple ion channels and action potential triangulation (APD(40-90)). Effects on repolarizing currents other than I(Kr) were also distinguished in guinea-pig VM.
QT间期延长和尖端扭转型室性心动过速(TdP)心律失常被认为是许多药物的潜在风险,其中大多数药物通过抑制快速激活的钾电流(I(Kr))来延迟心脏复极化。本研究的目的是比较化合物对豚鼠心室肌细胞和犬浦肯野纤维记录的心脏动作电位的影响。
研究了多非利特、索他洛尔、西沙必利、特非那定、氟哌啶醇和司帕沙星(已知可导致QT延长的化合物,作为阳性对照)以及硝苯地平和维拉帕米(与QT延长无关,作为阴性对照)对豚鼠离体心室肌细胞(VM)和犬离体浦肯野纤维(PF)记录的细胞内动作电位的影响。索他洛尔、多非利特和司帕沙星对动作电位时程(APD)的延长呈浓度依赖性,且在犬PF中比豚鼠VM中幅度更大。在0.5和1Hz时,豚鼠VM中APD的最大延长约为25%,这与多非利特对I(Kr)的完全抑制有关。西沙必利和氟哌啶醇在两种制剂中以及特非那定在豚鼠VM中对APD的影响是双相的,这与对多个离子通道的抑制一致。特非那定对犬PF中的APD没有影响。氟哌啶醇使豚鼠VM中的APD增加超过25%,这与对其他复极电流的影响一致。与犬PF相比,阴性对照在豚鼠VM中更显著地缩短了APD。一般来说,阳性对照药物比APD(90)更显著地增加动作电位三角化(APD(40-90))。
豚鼠离体VM对于检测抑制多个离子通道和动作电位三角化(APD(40-90))的化合物导致的APD延长可能更敏感。在豚鼠VM中也区分了对I(Kr)以外的复极电流的影响。