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阿尔茨海默病的线粒体级联假说:虚构还是现实?

Mitochondrial cascade hypothesis of Alzheimer's disease: myth or reality?

作者信息

Mancuso Michelangelo, Coppedè Fabio, Murri Luigi, Siciliano Gabriele

机构信息

Department of Neuroscience, Neurological Clinic, University of Pisa, Italy.

出版信息

Antioxid Redox Signal. 2007 Oct;9(10):1631-46. doi: 10.1089/ars.2007.1761.

Abstract

Mitochondria are recognized to play a pivotal role in neuronal cell survival or death because they are regulators of both energy metabolism and apoptotic pathways. Morphologic, biochemical, and molecular genetic studies suggest that mitochondria might be a convergence point for neurodegeneration, including Alzheimer's disease (AD). The functions and properties of mitochondria might render subsets of selectively vulnerable neurons intrinsically susceptible to cellular aging and stress. However, the question, "Is mitochondrial dysfunction a necessary step in neurodegeneration?" is still unanswered. This review presents the ways in which malfunctioning mitochondria and oxidative stress might contribute to neuronal death in AD.

摘要

线粒体被认为在神经元细胞的存活或死亡中起关键作用,因为它们是能量代谢和凋亡途径的调节者。形态学、生物化学和分子遗传学研究表明,线粒体可能是神经退行性变(包括阿尔茨海默病,即AD)的一个汇聚点。线粒体的功能和特性可能使某些易损神经元亚群在本质上易受细胞衰老和应激的影响。然而,“线粒体功能障碍是神经退行性变的必要步骤吗?”这个问题仍未得到解答。本综述介绍了功能失常的线粒体和氧化应激可能导致AD中神经元死亡的方式。

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