Abstract:
:Aging is characterized by decrements in maximum function and accumulation of mitochondrial DNA mutations, which are best observed in organs such as the brain that contain post-mitotic cells. Oxygen radicals are increasingly considered responsible for part of these aging changes. Comparative studies of animals with different aging rates have shown that the rate of mitochondrial oxygen radical generation is directly related to the steady-state level of oxidative damage to mitochondrial DNA and is inversely correlated with maximum longevity in higher vertebrates. The degree of unsaturation of tissue fatty acids also correlates inversely with maximum longevity. These are the two known traits connecting oxidative stress with aging. Furthermore, caloric restriction, which decreases the rate of aging, proportionately decreases mitochondrial oxygen radical generation, especially at complex I. These findings are reviewed, highlighting the results obtained in the brain.
journal_name
Trends Neuroscijournal_title
Trends in neurosciencesauthors
Barja Gdoi
10.1016/j.tins.2004.07.005subject
Has Abstractpub_date
2004-10-01 00:00:00pages
595-600issue
10eissn
0166-2236issn
1878-108Xpii
S0166-2236(04)00233-4journal_volume
27pub_type
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journal_title:Trends in neurosciences
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journal_title:Trends in neurosciences
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