Riva E, Hearse D J
Cardiovascular Research, Rayne Institute, St Thomas' Hospital, London.
Cardiovasc Res. 1989 Apr;23(4):331-9. doi: 10.1093/cvr/23.4.331.
The effects of amiodarone and its metabolite desethylamiodarone on arrhythmias induced by ischaemia and reperfusion were studied in vivo in the anaesthetised rat with transient regional ischaemia (7 min of left coronary artery occlusion) and reperfusion (10 min). Amiodarone or desethylamiodarone were administered intravenously either 10 min prior to ischaemia or 2 min prior to reperfusion. Control rats received an equivalent volume of vehicle. Administration of 5.0 mg.kg-1 amiodarone or desethylamiodarone prior to ischaemia reduced the incidence of ventricular tachycardia during the ischaemic period from 67% to 20% (p less than 0.02) and 47% respectively. During reperfusion, mortality was reduced from 53% to 7% and 7% (p less than 0.02) respectively, and reperfusion induced ventricular fibrillation from 73% to 20% (p less than 0.01) and 47% respectively. When the drugs were given prior to ischaemia, the plasma concentrations of amiodarone and desethylamiodarone were 1.03 (SEM 0.18) and 0.22(0.02) micrograms.ml-1 and the myocardial concentrations were 23.43(2.78) and 30.41(1.87) micrograms.g-1 respectively. Similar concentrations were found in plasma and myocardium with drugs given prior to reperfusion. No significant differences in plasma or myocardial concentrations of amiodarone or desethylamiodarone were observed between animals which developed ventricular fibrillation and those which did not. In conclusion, this study demonstrates that desethylamiodarone can, like its parent compound, protect the heart against malignant ventricular arrhythmias arising as a consequence of regional myocardial ischaemia and reperfusion.
在麻醉大鼠体内,采用短暂局部缺血(左冠状动脉闭塞7分钟)和再灌注(10分钟)的方法,研究了胺碘酮及其代谢产物去乙基胺碘酮对缺血再灌注所致心律失常的影响。胺碘酮或去乙基胺碘酮于缺血前10分钟或再灌注前2分钟静脉给药。对照组大鼠给予等量溶媒。缺血前给予5.0mg·kg-1胺碘酮或去乙基胺碘酮,可使缺血期室性心动过速的发生率分别从67%降至20%(p<0.02)和47%。再灌注期间,死亡率分别从53%降至7%和7%(p<0.02),再灌注诱发的心室颤动分别从73%降至20%(p<0.01)和47%。药物在缺血前给药时,胺碘酮和去乙基胺碘酮的血浆浓度分别为1.03(标准误0.18)和0.22(0.02)μg·ml-1,心肌浓度分别为23.43(2.78)和30.41(1.87)μg·g-1。再灌注前给药时,血浆和心肌中也发现了类似的浓度。发生心室颤动的动物与未发生心室颤动的动物在胺碘酮或去乙基胺碘酮的血浆或心肌浓度上未观察到显著差异。总之,本研究表明,去乙基胺碘酮与其母体化合物一样,可保护心脏免受局部心肌缺血和再灌注所致的恶性室性心律失常的影响。