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Mitochondrial dysfunction and oxidative stress in Parkinson's disease and monogenic parkinsonism

期刊

NEUROBIOLOGY OF DISEASE
卷 51, 期 -, 页码 35-42

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2012.10.011

关键词

Parkinson's disease; Mitochondria; Oxidative stress; Dopamine oxidation

资金

  1. Intramural Research Program of the NIH, National Institute on Aging
  2. NIH [NS059806]

向作者/读者索取更多资源

The pathogenic mechanisms that underlie Parkinson's disease remain unknown. Here, we review evidence from both sporadic and genetic forms of Parkinson's disease that implicate both mitochondria and oxidative stress as central players in disease pathogenesis. A systemic deficiency in complex I of the mitochondrial electron transport chain is evident in many patients with the disease. Oxidative stress caused by reactive metabolites of dopamine and alterations in the levels of iron and glutathione in the substantia nigra accompany this mitochondrial dysfunction. Recent evidence from studies on the genetic forms of parkinsonism with particular stress on DJ-1, parkin, and PINK-1 also suggest the involvement of mitochondria and oxidative stress. (C) 2012 Elsevier Inc. All rights reserved.

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