Farkas Attila S, Acsai Károly, Tóth András, Dézsi László, Orosz Szabolcs, Forster Tamás, Csanády Miklós, Papp Julius Gy, Varró András, Farkas András
2nd Department of Internal Medicine and Cardiology Centre, Faculty of Medicine, University of Szeged, Korányi fasor 6., Szeged, H-6701, Hungary.
Eur J Pharmacol. 2006 May 10;537(1-3):118-25. doi: 10.1016/j.ejphar.2006.03.014. Epub 2006 Mar 20.
In anaesthetized rabbits, alpha(1)-adrenoceptor stimulation increases the propensity of repolarization-prolonging drugs to induce torsade de pointes ventricular tachycardia. However, it is not known whether the stimulation of intracardiac alpha(1)-adrenoceptors, or the increased ventricular stretch caused by extracardiac alpha(1)-adrenoceptor-mediated peripheral vasoconstriction and increased resistance, are the sensitizing factors. Accordingly, this study investigated whether a sustained load-induced left ventricular stretch or stimulation of the intracardiac alpha(1)-adrenoceptors with 100 nM methoxamine, or the co-application of these two, can assist dofetilide (100 nM) to elicit torsade de pointes in isolated Langendorff-perfused, rabbit hearts. In the stretched hearts, a constant high level of stretch was produced by a water-filled left ventricular balloon inflated to a volume of 1.4 ml, whereby the systolic and end-diastolic pressures virtually did not exceed the physiological range (<or=157+/-11 mm Hg and <or=9+/-2 mm Hg, respectively; mean+/-S.E.M.). Perfusion with dofetilide prolonged the QT interval significantly and indifferently in all hearts. Neither this stretch nor methoxamine nor the in combination affected the QT interval, the heart rate or the coronary flow. Interestingly, neither the stretch ('dofetilide+stretch' group, n=8 hearts), nor methoxamine ('dofetilide+methoxamine' group, n=8 hearts), nor the in combination ('dofetilide+stretch+methoxamine' group, n=8 hearts) elevated the incidence of torsade de pointes as compared with the 'dofetilide alone' group (n=9 hearts) (0%, 25%, 0%, versus 44%, respectively). In conclusion, neither a sustained load-induced stretch nor alpha(1)-adrenoceptor stimulation nor the in combination assisted dofetilide to induce torsade de pointes in isolated rabbit hearts, suggesting the importance of extracardiac alpha(1)-adrenoceptor stimulation in this phenomenon.
在麻醉兔中,α₁肾上腺素受体刺激会增加延长复极药物诱发尖端扭转型室性心动过速的倾向。然而,尚不清楚是心内α₁肾上腺素受体的刺激,还是心外α₁肾上腺素受体介导的外周血管收缩和阻力增加所导致的心室牵张增加是致敏因素。因此,本研究调查了持续负荷诱导的左心室牵张、用100 nM甲氧明刺激心内α₁肾上腺素受体,或两者联合应用,是否能协助多非利特(100 nM)在离体Langendorff灌注兔心脏中诱发尖端扭转型室性心动过速。在牵张的心脏中,通过向充满水的左心室球囊充气至1.4 ml的体积产生恒定的高水平牵张,由此收缩压和舒张末期压力实际上均未超过生理范围(分别为≤157±11 mmHg和≤9±2 mmHg;平均值±标准误)。在所有心脏中,用多非利特灌注均显著且无差异地延长了QT间期。这种牵张、甲氧明或两者联合应用均不影响QT间期、心率或冠状动脉血流。有趣的是,与“单独使用多非利特”组(n = 9个心脏)相比,无论是牵张(“多非利特+牵张”组,n = 8个心脏)、甲氧明(“多非利特+甲氧明”组,n = 8个心脏)还是两者联合应用(“多非利特+牵张+甲氧明”组,n = 8个心脏),尖端扭转型室性心动过速的发生率均未升高(分别为0%、25%、0%,而单独使用多非利特组为44%)。总之,在离体兔心脏中,持续负荷诱导的牵张、α₁肾上腺素受体刺激或两者联合应用均不能协助多非利特诱发尖端扭转型室性心动过速,提示心外α₁肾上腺素受体刺激在这一现象中的重要性。