Nakamura T, Kashimoto S, Oguchi T, Kumazawa T
Department of Anesthesiology, Yamanashi Medical College, Japan.
Heart Vessels. 1992;7(4):169-74. doi: 10.1007/BF01744601.
We examined the effects of propafenone, a new anti-dysrhythmic agent, on myocardial function and metabolism in ischemic working rat heart preparations. In the treated hearts, propafenone, 0.3 micrograms/ml and 3 micrograms/ml, were added to Krebs-Henseleit bicarbonate buffer perfusate throughout the experiments. Whole heart ischemia was induced through a one-way aortic valve for 15 min followed by 'reperfusion for 30 min. After induction of ischemia, the cardiac output, peak aortic systolic pressure, left ventricular dP/dtmax, and myocardial ATP concentration were greater in the treated hearts than in the untreated ones. All hearts in the untreated group developed ventricular fibrillation (Vf) at the beginning of the reperfusion period. On the other hand, no treated hearts had Vf at any time during the experiment. However, propafenone, 3 micrograms/ml, evoked a negative inotropic effect before and after ischemia. These results indicate that propafenone may contribute to early recovery from ischemia in myocardial function and metabolism, although it has a negative inotropic action.
我们研究了新型抗心律失常药物普罗帕酮对缺血工作大鼠心脏标本心肌功能和代谢的影响。在处理过的心脏中,在整个实验过程中,将浓度为0.3微克/毫升和3微克/毫升的普罗帕酮添加到克雷布斯-亨泽莱特碳酸氢盐缓冲灌注液中。通过单向主动脉瓣诱导全心缺血15分钟,随后再灌注30分钟。缺血诱导后,处理过的心脏的心输出量、主动脉收缩压峰值、左心室dP/dtmax和心肌ATP浓度均高于未处理的心脏。未处理组的所有心脏在再灌注期开始时均发生心室颤动(Vf)。另一方面,处理过的心脏在实验期间的任何时候都没有发生Vf。然而,3微克/毫升的普罗帕酮在缺血前后均引起负性肌力作用。这些结果表明,普罗帕酮可能有助于心肌功能和代谢从缺血中早期恢复,尽管它具有负性肌力作用。