The emerging role of iron dyshomeostasis in the mitochondrial decay of aging.

Abstract:

:Recent studies show that cellular and mitochondrial iron increases with age. Iron overload, especially in mitochondria, increases the availability of redox-active iron, which may be a causal factor in the extensive age-related biomolecular oxidative damage observed in aged organisms. Such damage is thought to play a major role in the pathogenesis of iron overload diseases and age-related pathologies. Indeed, recent findings of the beneficial effects of iron manipulation in life extension in Caenorhabditis elegans, Drosophila and transgenic mice have sparked a renewed interest in the potential role of iron in longevity. A substantial research effort now focuses on developing and testing safe pharmacologic interventions to combat iron dyshomeostasis in aging, acute injuries and in iron overload disorders.

journal_name

Mech Ageing Dev

authors

Xu J,Marzetti E,Seo AY,Kim JS,Prolla TA,Leeuwenburgh C

doi

10.1016/j.mad.2010.04.007

subject

Has Abstract

pub_date

2010-07-01 00:00:00

pages

487-93

issue

7-8

eissn

0047-6374

issn

1872-6216

pii

S0047-6374(10)00089-8

journal_volume

131

pub_type

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