Correia Sónia C, Carvalho Cristina, Cardoso Susana, Santos Renato X, Santos Maria S, Oliveira Catarina R, Perry George, Zhu Xiongwei, Smith Mark A, Moreira Paula I
Center for Neuroscience and Cell Biology, University of Coimbra Coimbra, Portugal.
Front Aging Neurosci. 2010 Aug 26;2. doi: 10.3389/fnagi.2010.00138. eCollection 2010.
Mitochondria have long been known as the powerhouse of the cell. However, these organelles are also pivotal players in neuronal cell death. Mitochondrial dysfunction is a prominent feature of chronic brain disorders, including Alzheimer's disease (AD) and Parkinson's disease (PD), and cerebral ischemic stroke. Data derived from morphologic, biochemical, and molecular genetic studies indicate that mitochondria constitute a convergence point for neurodegeneration. Conversely, mitochondria have also been implicated in the neuroprotective signaling processes of preconditioning. Despite the precise molecular mechanisms underlying preconditioning-induced brain tolerance are still unclear, mitochondrial reactive oxygen species generation and mitochondrial ATP-sensitive potassium channels activation have been shown to be involved in the preconditioning phenomenon. This review intends to discuss how mitochondrial malfunction contributes to the onset and progression of cerebral ischemic stroke and AD and PD, two major neurodegenerative disorders. The role of mitochondrial mechanisms involved in the preconditioning-mediated neuroprotective events will be also discussed. Mitochondrial targeted preconditioning may represent a promising therapeutic weapon to fight neurodegeneration.
长期以来,线粒体一直被认为是细胞的动力源。然而,这些细胞器在神经元细胞死亡中也是关键因素。线粒体功能障碍是包括阿尔茨海默病(AD)、帕金森病(PD)和脑缺血性中风在内的慢性脑部疾病的一个显著特征。来自形态学、生物化学和分子遗传学研究的数据表明,线粒体是神经退行性变的一个汇聚点。相反,线粒体也参与了预处理的神经保护信号过程。尽管预处理诱导脑耐受的精确分子机制仍不清楚,但线粒体活性氧的产生和线粒体ATP敏感性钾通道的激活已被证明与预处理现象有关。本综述旨在讨论线粒体功能障碍如何导致脑缺血性中风以及AD和PD这两种主要神经退行性疾病的发生和发展。还将讨论线粒体机制在预处理介导的神经保护事件中的作用。线粒体靶向预处理可能是对抗神经退行性变的一种有前景的治疗手段。