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盐酸索他洛尔在马体内的药代动力学及电生理效应

Pharmacokinetics and electrophysiological effects of sotalol hydrochloride in horses.

作者信息

Broux B, De Clercq D, Decloedt A, Vera L, Devreese M, Gehring R, Croubels S, van Loon G

机构信息

Department of Large Animal Internal Medicine, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

Department of Pharmacology, Toxicology and Biochemistry, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

出版信息

Equine Vet J. 2018 May;50(3):377-383. doi: 10.1111/evj.12765. Epub 2017 Nov 1.

Abstract

BACKGROUND

Arrhythmias in horses may require long-term anti-arrhythmic therapy. Unfortunately, oral anti-arrhythmic drugs for use in horses are currently scarce. In human patients and small animals, sotalol, a β-blocker with class III anti-arrhythmic properties, is often used for long-term treatment.

OBJECTIVES

To determine the pharmacokinetics of sotalol at multiple oral dosages in unfasted horses, as well as the effects on electro- and echocardiographic measurements, right atrial and ventricular monophasic action potential (MAP) and effective refractory period (ERP).

STUDY DESIGN

Placebo controlled, double-blinded experiment.

MATERIALS AND METHODS

Six healthy, unfasted Warmblood horses were given either 0, 2, 3 or 4 mg/kg bodyweight (bwt) sotalol orally (PO) twice daily (bid) for 9 days in a randomised cross-over design. Echocardiography and surface electrocardiography were performed and plasma concentrations of sotalol and right atrial and right ventricular MAPs and ERPs were determined at steady-state conditions. Statistical analysis was performed using a repeated measures univariate analysis with post hoc Bonferroni corrections.

RESULTS

Calculated mean steady-state plasma concentrations determined by nonlinear mixed-effect modelling were 287 (range 234-339), 409 (359-458) and 543 (439-646) ng/mL for 2, 3 and 4 mg/kg bwt sotalol PO bid respectively. Sotalol significantly increased the QT interval and ERPs, but, despite increasing plasma concentrations, higher dosages did not result in a progressive increase in QT interval or ERPs. Echocardiographic and other electrocardiographic measurements did not change significantly. MAP durations at 90% repolarisation were not significantly different during sotalol treatment. Besides transient local sweating, no side effects were noted.

MAIN LIMITATIONS

Study size and ad libitum feeding of hay.

CONCLUSIONS

Sotalol at a dose of 2, 3 and 4 mg/kg bwt PO bid increases the QT interval and ERP and might be a useful drug for long-term anti-arrhythmic therapy in horses.

摘要

背景

马匹心律失常可能需要长期抗心律失常治疗。遗憾的是,目前用于马匹的口服抗心律失常药物稀缺。在人类患者和小动物中,索他洛尔是一种具有Ⅲ类抗心律失常特性的β受体阻滞剂,常用于长期治疗。

目的

确定索他洛尔在未禁食马匹中的多种口服剂量的药代动力学,以及对心电图和超声心动图测量、右心房和心室单相动作电位(MAP)及有效不应期(ERP)的影响。

研究设计

安慰剂对照、双盲实验。

材料与方法

采用随机交叉设计,6匹健康、未禁食的温血马每天口服(PO)两次,每次给予0、2、3或4mg/kg体重(bwt)的索他洛尔,持续9天。在稳态条件下进行超声心动图和体表心电图检查,并测定索他洛尔的血浆浓度以及右心房和右心室的MAP和ERP。使用重复测量单变量分析及事后Bonferroni校正进行统计分析。

结果

通过非线性混合效应模型计算的平均稳态血浆浓度,2、3和4mg/kg bwt索他洛尔PO bid分别为287(范围234 - 339)、409(359 - 458)和543(439 - 646)ng/mL。索他洛尔显著增加QT间期和ERP,但尽管血浆浓度升高,更高剂量并未导致QT间期或ERP的逐渐增加。超声心动图和其他心电图测量无显著变化。索他洛尔治疗期间,90%复极化时的MAP持续时间无显著差异。除了短暂的局部出汗外,未观察到副作用。

主要局限性

研究规模和随意喂食干草。

结论

2、3和4mg/kg bwt PO bid剂量的索他洛尔可增加QT间期和ERP,可能是马匹长期抗心律失常治疗的有用药物。

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