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自噬在心肌再灌注损伤中的作用。

Role of autophagy in myocardial reperfusion injury.

作者信息

Jin Yulan, Wang Huihua, Cui Xun, Jin Yuanzhe, Xu Zhelong

机构信息

Department of Physiology, Yanbian University, Yanji, China.

出版信息

Front Biosci (Elite Ed). 2010 Jun 1;2(3):1147-53. doi: 10.2741/e174.

Abstract

While autophagy is induced by myocardial ischemia/reperfusion, it is unclear whether autophagy is detrimental or beneficial to myocardial survival during ischemia/reperfusion. Isolated rat hearts were subjected to 30 min regional ischemia followed by 2 h of reperfusion. Autophagy was determined by the ratio of LC3 -II to LC3-I with Western blotting. Autophagy was prominent upon reperfusion but not during ischemia in rat hearts, indicating that autophagy may play a role during reperfusion phase. Ischemia or reperfusion did not enhance Beclin 1 expression, suggesting that Beclin 1 may not be critical for the formation of autophagy in isolated rat hearts. 3-methyladenine (3-MA), a classical inhibitor of autophagy, suppressed reperfusion-induced autophagy and reduced the infarct size when introduced at reperfusion. NECA, an agonist of adenosine receptors, and morphine also reduced the formation of autophagy as well as the infarct size when introduced at reperfusion. These data suggest that autophagy may play a detrimental role during reperfusion and that modulation of autophagy may prevent.

摘要

虽然自噬由心肌缺血/再灌注诱导,但目前尚不清楚自噬在缺血/再灌注期间对心肌存活是有害还是有益。将离体大鼠心脏进行30分钟的局部缺血,随后再灌注2小时。通过蛋白质免疫印迹法检测LC3-II与LC3-I的比值来确定自噬。在大鼠心脏中,自噬在再灌注时明显,但在缺血期间不明显,这表明自噬可能在再灌注阶段起作用。缺血或再灌注并未增强Beclin 1的表达,这表明Beclin 1可能对离体大鼠心脏中自噬的形成并不关键。3-甲基腺嘌呤(3-MA)是一种经典的自噬抑制剂,在再灌注时使用可抑制再灌注诱导的自噬并减小梗死面积。腺苷受体激动剂NECA以及吗啡在再灌注时使用也可减少自噬的形成以及梗死面积。这些数据表明自噬在再灌注期间可能起有害作用,并且对自噬的调节可能具有预防作用。

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