Shin Il Woo, Cho Man Seok, Jang In Seok, Sohn Ju Tae, Lee Heon Keun, Chung Young Kyun
Department of Anesthesiology and Pain Medicine, College of Medicine, Gyeongsang National University, Jinju, Korea.
Korean J Anesthesiol. 2009 Aug;57(2):190-194. doi: 10.4097/kjae.2009.57.2.190.
It is known that some opioids protect the myocardial tissue from myocardial ischemia-reperfusion (I/R) injury. The aim of this study was to investigate whether remifentanil, at a clinically relevant concentration that's during the peri-ischemic period, has a protective effect against a regional I/R injury in an in vivo rat heart model.
Rats were subjected to 25 minutes of coronary artery occlusion and this was followed by 24 hours of reperfusion. A microcatheter was advanced into the left ventricle and the hemodynamic function was evaluated after 24 hours of reperfusion. The infarct size was determined by triphenyltetrazolium staining. The serum level of cardiac troponin-I (cTnI) was determined by ELISA (enzyme-linked immunosorbent assay).
Remifentanil administration during the peri-ischemic period didn't show any identifiable protective effects for the hemodynamic function or to reduce the infarct size. In the control group, the peak rate of the ventricular pressure increase (+dP/dt(max)) (P < 0.05) and the peak rate of the intraventricular pressure decline (-dP/dt(max) P < 0.05) were significantly decreased as compared to those values for the sham group. In the remifentanil group, the +dP/dt(max) and -dP/dt(max) were not improved compared to those values of the control group. The infarct size was 45.6% of the area at risk in the control group, and the infarct size was reduced by administration of remifentanil to 43.2% in the remifentanil group. The I/R-induced serum level of cTn-I was not reduced by remifentanil infusion during the peri-ischemic period.
Remifentanil, at a clinically relevant concentration that's infused during the peri-ischemic period, has no myocardial protective effect after regional myocardial I/R injury in an in vivo rat heart model.
已知某些阿片类药物可保护心肌组织免受心肌缺血-再灌注(I/R)损伤。本研究的目的是探讨在围缺血期给予临床相关浓度的瑞芬太尼,是否对体内大鼠心脏模型的局部I/R损伤具有保护作用。
对大鼠进行25分钟的冠状动脉闭塞,随后进行24小时的再灌注。将微导管插入左心室,并在再灌注24小时后评估血流动力学功能。通过三苯基四氮唑染色确定梗死面积。采用酶联免疫吸附测定法(ELISA)测定血清心肌肌钙蛋白I(cTnI)水平。
在围缺血期给予瑞芬太尼对血流动力学功能或减小梗死面积未显示出任何可识别的保护作用。在对照组中,与假手术组相比,心室压力上升峰值速率(+dP/dt(max))(P<0.05)和室内压下降峰值速率(-dP/dt(max),P<0.05)显著降低。在瑞芬太尼组中,与对照组相比,+dP/dt(max)和-dP/dt(max)未得到改善。对照组梗死面积为危险区面积的45.6%,瑞芬太尼组给予瑞芬太尼后梗死面积降至43.2%。围缺血期输注瑞芬太尼并未降低I/R诱导的血清cTn-I水平。
在围缺血期给予临床相关浓度的瑞芬太尼,在体内大鼠心脏模型中,局部心肌I/R损伤后没有心肌保护作用。