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Mitochondrial preconditioning: a potential neuroprotective strategy

期刊

FRONTIERS IN AGING NEUROSCIENCE
卷 2, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2010.00138

关键词

mitochondria; mitoK(ATP) channels; neurodegeneration; neuroprotection; preconditioning; reactive oxygen species

资金

  1. European Foundation for the Study of Diabetes/Servier
  2. Fundacao para a Ciencia e a Tecnologia [SFRH/BD/40702/2007]
  3. Fundação para a Ciência e a Tecnologia [SFRH/BD/40702/2007] Funding Source: FCT

向作者/读者索取更多资源

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.

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