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胺碘酮和决奈达隆治疗对兔模型心脏功能的比较效应

Comparative effects of amiodarone and dronedarone treatments on cardiac function in a rabbit model.

作者信息

Boonhoh Worakan, Kijtawornrat Anusak, Sawangkoon Suwanakiet

机构信息

Department of Physiology, Animal Physiology Program, Faculty of Veterinary Science, Chulalongkorn University, 39 Henri Dunant Road, Pathumwan, Bangkok 10330, Thailand.

Department of Physiology, Faculty of Veterinary Science, Chulalongkorn University, 39 Henri Dunant Road, Pathumwan, Bangkok 10330, Thailand.

出版信息

Vet World. 2019;12(2):345-351. doi: 10.14202/vetworld.2019.345-351. Epub 2019 Feb 28.

Abstract

AIM

The objective of the study was to compare the effects of amiodarone (AM) and dronedarone (DR) on heart rate variability (HRV) and cardiac contractility in a rabbit model.

MATERIALS AND METHODS

A total of 16 male New Zealand white rabbits were divided into two groups, treated either with AM or DR at incremental dosages of 50 mg/kg/day (AM50 and DR50) and 100 mg/kg/day (AM100 and DR100), orally administrated for 7 days. At the end of each period, electrocardiograms were recorded during consciousness and analyzed using the short-term time and frequency domains of HRV. Standard echocardiography and speckle-tracking echocardiography were studied during immobilization with xylazine and ketamine.

RESULTS

The results showed that AM100 and DR100 significantly decreased heart rate, total power, low-frequency component, and low-to-high frequency ratio compared with baselines. Most echocardiogram parameters revealed no significant difference from baselines, except for the global circumferential plane strain rate and time to peak standard deviation of strain, which had statistical significances after treating with AM.

CONCLUSION

Both AM and DR possess negative chronotropy and reduce HRV, which may be explained by their sympathetic suppression and calcium channel blocking activities. Theoretically, both antiarrhythmic drugs may also possess negative inotropy, but only AM is shown to have a negative inotropic effect and reduces cardiac dyssynchrony in this model.

摘要

目的

本研究的目的是在兔模型中比较胺碘酮(AM)和决奈达隆(DR)对心率变异性(HRV)和心脏收缩力的影响。

材料与方法

总共16只雄性新西兰白兔被分为两组,分别用50mg/kg/天(AM50和DR50)和100mg/kg/天(AM100和DR100)的递增剂量的AM或DR进行治疗,口服给药7天。在每个阶段结束时,在清醒状态下记录心电图,并使用HRV的短期时域和频域进行分析。在用赛拉嗪和氯胺酮麻醉固定期间进行标准超声心动图和斑点追踪超声心动图检查。

结果

结果显示,与基线相比,AM100和DR100显著降低了心率、总功率、低频成分和低频与高频比值。大多数超声心动图参数与基线相比无显著差异,但整体圆周平面应变率和应变峰值标准差时间除外,在用AM治疗后这些参数具有统计学意义。

结论

AM和DR均具有负性变时性并降低HRV,这可能与其交感神经抑制和钙通道阻滞活性有关。理论上,这两种抗心律失常药物也可能具有负性变力性,但在该模型中仅AM显示具有负性变力性并减少心脏不同步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6cd/6460874/62ecab2bfa60/Vetworld-12-345-g001.jpg

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