Department of Cardiology; Xijing Hospital; Fourth Military Medical University; Xi'an, China; Center for Cardiovascular Research and Alternative Medicine; University of Wyoming; Laramie, WY USA.
Autophagy. 2010 Nov;6(8):1212-3. doi: 10.4161/auto.6.8.13652. Epub 2010 Nov 16.
The mitochondrial isoform of aldehyde dehydrogenase (ALDH2) plays a key role in the metabolism of acetaldehyde and other toxic aldehydes. A recent seminal finding has indicated a potential role of ALDH2 activation in the cardioprotection against ischemic injury. Data from our group unveiled a myocardial protective effect of ALDH2 against ischemia/reperfusion (I/R) injury possibly through detoxification of toxic aldehydes: and a differential regulation of autophagy mediated by AMPK-mTOR and Akt-mTOR signaling cascades during ischemia and reperfusion, respectively. These findings suggest not only the therapeutic potential of ALDH2 against I/R injury but also a pivotal role of the AMPK-Akt-mTOR signaling in the paradoxical autophagic regulation of cardiomyocyte survival.
线粒体同工型乙醛脱氢酶(ALDH2)在乙醛和其他有毒醛类的代谢中起着关键作用。最近的一项重要发现表明,ALDH2 的激活可能在心肌缺血损伤的保护中发挥作用。我们小组的数据揭示了 ALDH2 对缺血/再灌注(I/R)损伤的心肌保护作用,可能是通过解毒有毒醛类实现的:以及在缺血和再灌注期间,分别通过 AMPK-mTOR 和 Akt-mTOR 信号级联对自噬进行的差异调节。这些发现不仅表明了 ALDH2 治疗 I/R 损伤的潜力,而且还表明了 AMPK-Akt-mTOR 信号在心肌细胞存活的矛盾性自噬调节中的关键作用。