論文

査読有り 筆頭著者 責任著者
2005年3月

Antiarrhythmic properties of a prior oral loading of amiodarone in in vivo canine coronary ligation/reperfusion-induced arrhythmia model: comparison with other class III antiarrhythmic drugs.

Journal of pharmacological sciences
  • Yoshinobu Nagasawa
  • ,
  • Jianguang Chen
  • ,
  • Keitaro Hashimoto

97
3
開始ページ
393
終了ページ
9
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1254/jphs.FP0040512
出版者・発行元
JAPANESE PHARMACOLOGICAL SOC

Amiodarone, which is generally classified as class III antiarrhythmic drug in the Vaughan Williams classification, is widely used for the treatments of refractory arrhythmias. However, we previously reported that intravenous infusion of amiodarone (6.67 mg/kg per hour) did not suppress arrhythmias induced by coronary ligation/reperfusion in dogs. In this study, we examined effects of a prior oral loading of amiodarone on arrhythmias induced by coronary ligation/reperfusion. Sixteen female beagle dogs (8.5 - 12.5 kg) were divided into two groups; one group was given amiodarone (40 mg/kg, orally, n = 8), and the other was given empty gelatin capsules (n = 8) 2 h before the operation. Dogs were anesthetized with pentobarbital and artificially ventilated. The left chest was opened, and the left anterior descending coronary artery was ligated for 30 min and then reperfused. The mean plasma concentration of amiodarone was over 1.3 mug/ml. Although the prior oral loading of amiodarone did not change the QT interval, amiodarone suppressed the number of ectopic beats during coronary ligation and the incidence of ventricular fibrillation during coronary ligation and reperfusion periods (P<0.05 vs control group). In conclusion, a prior oral loading of amiodarone suppressed arrhythmias induced by coronary ligation/reperfusion with a dose that did not prolong the QT interval. This antiarrhythmic property of amiodarone is different from those of the other class III drugs in that antiarrhythmic effects were accompanied by QT prolongation in our all previous studies.

リンク情報
DOI
https://doi.org/10.1254/jphs.FP0040512
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/15764841
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000227959700014&DestApp=WOS_CPL
ID情報
  • DOI : 10.1254/jphs.FP0040512
  • ISSN : 1347-8613
  • PubMed ID : 15764841
  • Web of Science ID : WOS:000227959700014

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