Simpkins James W, Yi Kun Don, Yang Shao-Hua, Dykens James A
Department of Pharmacology & Neuroscience, Institute for Aging and Alzheimer's Disease Research, University of North Texas Health Science Center, Fort Worth, TX, USA.
Biochim Biophys Acta. 2010 Oct;1800(10):1113-20. doi: 10.1016/j.bbagen.2009.11.013. Epub 2009 Nov 26.
Mitochondria have become a primary focus in our search not only for the mechanism(s) of neuronal death but also for neuroprotective drugs and therapies that can delay or prevent Alzheimer's disease and other chronic neurodegenerative conditions. This is because mitochrondria play a central role in regulating viability and death of neurons, and mitochondrial dysfunction has been shown to contribute to neuronal death seen in neurodegenerative diseases. In this article, we review the evidence for the role of mitochondria in cell death and neurodegeneration and provide evidence that estrogens have multiple effects on mitochondria that enhance or preserve mitochondrial function during pathologic circumstances such as excitotoxicity, oxidative stress, and others. As such, estrogens and novel non-hormonal analogs have come to figure prominently in our efforts to protect neurons against both acute brain injury and chronic neurodegeneration.
线粒体不仅已成为我们探寻神经元死亡机制的主要焦点,还成为了寻找可延缓或预防阿尔茨海默病及其他慢性神经退行性疾病的神经保护药物和疗法的主要焦点。这是因为线粒体在调节神经元的存活和死亡中起着核心作用,并且线粒体功能障碍已被证明与神经退行性疾病中所见的神经元死亡有关。在本文中,我们综述了线粒体在细胞死亡和神经退行性变中作用的证据,并提供证据表明雌激素在诸如兴奋性毒性、氧化应激等病理情况下对线粒体具有多种作用,可增强或维持线粒体功能。因此,雌激素和新型非激素类似物在我们保护神经元免受急性脑损伤和慢性神经退行性变的努力中已变得至关重要。