The cellular and molecular mechanisms that underlie cardioprotection against I/R by anesthetic-induced preconditioning (APC) require further elucidation. Using isoflurane as a representative anesthetic, we evaluated the hypothesis that APC induces myocardial protection against I/R by attenuation of excessive reactive oxygen species and restoration of mitochondrial bioenergetics through postischemic up-regulation of manganese superoxide dismutase (MnSOD) expression and preservation of respiratory enzyme activity. Pentobarbital anesthetized open-chest Sprague-Dawley rats were subject to 30-min left coronary artery occlusion, followed by 120-min reperfusion. Before ischemia, rats were randomly assigned to receive 0.9% saline, two cycles of brief coronary artery occlusion and reperfusion, or a 30-min exposure to 1.0 minimum alveolar concentration isoflurane in the absence or presence of a specific mitochondrial adenosine triphosphate-sensitive potassium (KATP) channel blocker, 5-hydroxydecanoate; a membrane-permeable superoxide scavenger, 4-hydroxy-2,2,6,6-tetramethyl piperidinoxyl; or a NOS inhibitor, N(G)-nitro-L-arginine methyl ester. Isoflurane exposure induced an initial increase in myocardial superoxide (O2-), but not NO level. It also significantly decreased infarct size and restored mitochondrial respiratory enzyme activity or ATP production in I/R rat hearts, along with suppression of the O2- surge at reperfusion and increase in MnSOD expression or enzyme activity. These protective effects were abrogated by 5-hydroxydecanoate or 4-hydroxy-2,2,6,6-tetramethyl piperidinoxyl, but not by N(G)-nitro-L-arginine methyl ester pretreatment. These results suggest that opening of mitochondrial KATP channel, followed by O2- signaling, induces postischemic augmentation of MnSOD and preservation of mitochondrial respiratory enzyme activities, leading to attenuated cardiac O2- surge and restored ATP production during reperfusion, and underlie APC-induced cardioprotection.

译文

麻醉诱导的预处理 (APC) 对I/R心脏保护的细胞和分子机制需要进一步阐明。使用异氟烷作为代表性麻醉剂,我们评估了以下假设: APC通过抑制过多的活性氧种类和线粒体生物能的恢复来诱导心肌对I/R的保护。通过有计划后上调锰超氧化物歧化酶 (MnSOD) 的表达和保留呼吸酶活性。对戊巴比妥麻醉的开胸Sprague-Dawley大鼠进行30分钟的左冠状动脉闭塞,然后进行120分钟的再灌注。缺血前,将大鼠随机分配接受0.9% 生理盐水,两个周期的短暂冠状动脉闭塞和再灌注,或在不存在或存在特定线粒体三磷酸腺苷敏感钾 (KATP) 通道阻滞剂5-羟基癸酸盐的情况下暴露于1.0最低肺泡浓度异氟烷30分钟; 膜可渗透的超氧化物清除剂,4-羟基-2,6,6-四甲基哌啶氧基; 或NOS抑制剂,N(G)-硝基-L-精氨酸甲酯。异氟烷暴露导致心肌超氧化物 (O2-) 的初始增加,但没有水平。它还显着减少了I/R大鼠心脏的梗塞面积并恢复了线粒体呼吸酶活性或ATP产生,并抑制了再灌注时的O2激增并增加了MnSOD表达或酶活性。这些保护作用通过5-羟基癸酸酯或4-羟基-2,6,6-四甲基哌啶氧基消除,但不通过N(G)-硝基-L-精氨酸甲酯预处理消除。这些结果表明,线粒体KATP通道的开放,随后是O2信号传导,可诱导MnSOD的缺血后增强和线粒体呼吸酶活性的保留,从而导致心脏O2激增减弱并在再灌注过程中恢复ATP的产生,并成为APC诱导的心脏保护的基础。

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