Piotrowski Roman, Giebułtowicz Joanna, Baran Jakub, Sikorska Agnieszka, Gralak-Łachowska Dagmara, Soszyńska Małgorzata, Wroczyński Piotr, Kułakowski Piotr
Department of Cardiology, Postgraduate Medical School, Grochowski Hospital, Warsaw, Poland.
Bioanalysis and Drugs Analysis Department, Faculty of Pharmacy, Medical University of Warsaw, Warsaw, Poland.
Ann Noninvasive Electrocardiol. 2017 Sep;22(5). doi: 10.1111/anec.12441. Epub 2017 Feb 25.
Antazoline is an old antihistaminic and new antiarrhythmic agent with unknown mechanisms of action which recently has been shown to effectively terminate atrial fibrillation. The aim of study was to examine the effects of antazoline on hemodynamic and ECG parameters.
Antazoline was given intravenously in three 100 mg boluses to 10 healthy volunteers (four males, mean age 40 + 11 years). Hemodynamic and ECG parameters were measured using impedance cardiography [systolic (sBP), diastolic (dBP), mean (mBP) blood pressure, stroke volume (SV), cardiac output (CO), total peripheral resistance (TPR) and heart rate (HR), P wave, PR interval, QRS complex, QT and corrected QT (QTcF) interval]. Plasma concentration of antazoline was also measured.
Antazoline caused significant prolongation of P wave, QRS as well as QT and QTcF (101 ± 10 vs 110 ± 16 ms, p < .05, and 101 ± 12 vs 107 ± 12 ms, p < .05, 399 ± 27 vs 444 ± 23 ms, p < .05, and 403 ± 21 vs 448 ± 27 ms, p < .05, respectively). Also, a significant decrease in SV was noted (94.9 ± 21.8 vs 82.4 ± 19.6 ml, p < .05). A significant correlation between changes in plasma drug concentration and changes in CO, HR, and dBP was found.
Antazoline impairs slightly hemodynamics, significantly reducing SV. Significant prolongation of P wave and QRS duration corresponds to drug-induced prolongation of conduction, whereas QT prolongation represents drug-induced prolongation of repolarization.
安他唑啉是一种作用机制不明的旧抗组胺药和新型抗心律失常药,最近已被证明能有效终止房颤。本研究的目的是检测安他唑啉对血流动力学和心电图参数的影响。
对10名健康志愿者(4名男性,平均年龄40±11岁)静脉注射三次100mg的安他唑啉。使用阻抗心动图测量血流动力学和心电图参数[收缩压(sBP)、舒张压(dBP)、平均血压(mBP)、每搏输出量(SV)、心输出量(CO)、总外周阻力(TPR)和心率(HR)、P波、PR间期、QRS波群、QT间期和校正QT(QTcF)间期]。还测量了安他唑啉的血浆浓度。
安他唑啉导致P波、QRS波以及QT和QTcF显著延长(分别为101±10对110±16ms,p<.05;101±12对107±12ms,p<.05;399±27对444±23ms,p<.05;403±21对448±27ms,p<.05)。此外,还观察到每搏输出量显著降低(94.9±21.8对82.4±19.6ml,p<.05)。发现血浆药物浓度变化与心输出量、心率和舒张压变化之间存在显著相关性。
安他唑啉对血流动力学有轻微损害,显著降低每搏输出量。P波和QRS波持续时间的显著延长对应于药物诱导的传导延长,而QT延长代表药物诱导的复极化延长。