Department of Anesthesiology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
J Zhejiang Univ Sci B. 2010 Apr;11(4):267-74. doi: 10.1631/jzus.B0900390.
Ischemic preconditioning and postconditioning distinctly attenuate ventricular arrhythmia after ischemia without affecting the severity of myocardial stunning. Therefore, we report the effects of sevoflurane preconditioning and postconditioning on stunned myocardium in isolated rat hearts. Isolated rat hearts were underwent 20 min of global ischemia and 40 min of reperfusion. After an equilibration period (20 min), the hearts in the preconditioning group were exposed to sevoflurane for 5 min and next washout for 5 min before ischemia. Hearts in the sevoflurane postconditioning group underwent equilibration and ischemia, followed immediately by sevoflurane exposure for the first 5 min of reperfusion. The control group received no treatment before and after ischemia. Left ventricular pressure, heart rate, coronary flow, electrocardiogram, and tissue histology were measured as variables of ventricular function and cellular injury, respectively. There was no significant difference in the duration of reperfusion ventricular arrhythmias between control and sevoflurane preconditioning group (P=0.195). The duration of reperfusion ventricular arrhythmias in the sevoflurane postconditioning group was significantly shorter than that in the other two groups (P<0.05). +/-(dP/dt)(max) in the sevoflurane preconditioning group at 5, 10, 15, 20, and 30 min after reperfusion was significantly higher than that in the control group (P<0.05), and there were no significant differences at 40 min after reperfusion among the three groups (P>0.05). As expected, for a 20-min general ischemia, infarct size in heart slices determined by 2,3,5-triphenyltetrazolium chloride staining among the groups was not obvious. Sevoflurane postconditioning reduces reperfusion arrhythmias without affecting the severity of myocardial stunning. In contrast, sevoflurane preconditioning has no beneficial effects on reperfusion arrhythmias, but it is in favor of improving ventricular function and recovering myocardial stunning. Sevoflurane preconditioning and postconditioning may be useful for correcting the stunned myocardium.
缺血预处理和后处理明显减弱缺血后室性心律失常而不影响心肌顿抑的严重程度。因此,我们报告七氟醚预处理和后处理对分离大鼠心脏顿抑心肌的影响。分离的大鼠心脏经历 20 分钟的全局缺血和 40 分钟的再灌注。在平衡期(20 分钟)后,预处理组的心脏暴露于七氟醚 5 分钟,然后在缺血前再洗脱 5 分钟。七氟醚后处理组的心脏经历平衡和缺血,随后立即在再灌注的前 5 分钟内暴露于七氟醚。对照组在缺血前后均未接受治疗。左心室压力、心率、冠状动脉流量、心电图和组织学分别作为心室功能和细胞损伤的变量进行测量。对照组和七氟醚预处理组之间再灌注室性心律失常的持续时间没有显著差异(P=0.195)。七氟醚后处理组的再灌注室性心律失常持续时间明显短于其他两组(P<0.05)。再灌注后 5、10、15、20 和 30 分钟,七氟醚预处理组的 +/-(dP/dt)(max)明显高于对照组(P<0.05),再灌注后 40 分钟三组之间无显著差异(P>0.05)。正如预期的那样,对于 20 分钟的一般缺血,各组通过 2,3,5-三苯基氯化四唑染色确定的心脏切片中的梗塞面积并不明显。七氟醚后处理减少再灌注心律失常而不影响心肌顿抑的严重程度。相比之下,七氟醚预处理对再灌注心律失常没有有益影响,但有利于改善心室功能和恢复心肌顿抑。七氟醚预处理和后处理可能有助于纠正顿抑心肌。