Department of Medical Biochemistry, Semmelweis University, Neurobiochemical Group of Hungarian Academy of Sciences, Budapest, Hungary.
J Alzheimers Dis. 2010;20 Suppl 2(Suppl 2):S413-26. doi: 10.3233/JAD-2010-100465.
A number of recent discoveries indicate that abnormal Ca2+ signaling, oxidative stress, and mitochondrial dysfunction are involved in the neuronal damage in Alzheimer's disease. However, the literature on the interactions between these factors is controversial especially in the interpretation of the cause-effect relationship between mitochondrial damage induced by Ca2+ overload and the production of reactive oxygen species (ROS). In this review, we survey the experimental observations on the Ca2+-induced mitochondrial ROS production, explain the sources of controversy in interpreting these results, and discuss the different molecular mechanisms underlying the effect of Ca2+ on the ROS emission by brain mitochondria.
一些最近的发现表明,异常的 Ca2+ 信号转导、氧化应激和线粒体功能障碍与阿尔茨海默病中的神经元损伤有关。然而,关于这些因素之间相互作用的文献存在争议,特别是在解释 Ca2+ 过载引起的线粒体损伤与活性氧(ROS)产生之间的因果关系时。在这篇综述中,我们调查了关于 Ca2+ 诱导的线粒体 ROS 产生的实验观察结果,解释了在解释这些结果时产生争议的原因,并讨论了 Ca2+ 对脑线粒体 ROS 发射的不同分子机制。