Szeto Hazel H
Department of Pharmacology, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021, USA.
AAPS J. 2006 Aug 18;8(3):E521-31. doi: 10.1208/aapsj080362.
Increasing evidence suggests that mitochondrial dysfunction and oxidative stress play a crucial role in the majority of neurodegenerative diseases. Mitochondria are a major source of intracellular reactive oxygen species (ROS) and are particularly vulnerable to oxidative stress. Oxidative damage to mitochondria has been shown to impair mitochondrial function and lead to cell death via apoptosis and necrosis. Because dysfunctional mitochondria will produce more ROS, a feed-forward loop is set up whereby ROS-mediated oxidative damage to mitochondria favors more ROS generation, resulting in a vicious cycle. It is now appreciated that reduction of mitochondrial oxidative stress may prevent or slow down the progression of these neurodegenerative disorders. However, if mitochondria are the major source of intracellular ROS and mitochondria are most vulnerable to oxidative damage, then it would be ideal to deliver the antioxidant therapy to mitochondria. This review will summarize the development of a novel class of mitochondria-targeted antioxidants that can protect mitochondria against oxidative stress and prevent neuronal cell death in animal models of stroke, Parkinson's disease, and amyotrophic lateral sclerosis.
越来越多的证据表明,线粒体功能障碍和氧化应激在大多数神经退行性疾病中起着关键作用。线粒体是细胞内活性氧(ROS)的主要来源,特别容易受到氧化应激的影响。线粒体的氧化损伤已被证明会损害线粒体功能,并通过凋亡和坏死导致细胞死亡。由于功能失调的线粒体将产生更多的ROS,因此会形成一个前馈循环,即ROS介导的线粒体氧化损伤有利于产生更多的ROS,从而导致恶性循环。现在人们认识到,降低线粒体氧化应激可能会预防或减缓这些神经退行性疾病的进展。然而,如果线粒体是细胞内ROS的主要来源,并且线粒体最容易受到氧化损伤,那么将抗氧化治疗递送至线粒体将是理想的。这篇综述将总结一类新型线粒体靶向抗氧化剂的发展,这类抗氧化剂可以保护线粒体免受氧化应激,并在中风、帕金森病和肌萎缩侧索硬化症的动物模型中预防神经元细胞死亡。