4.7 Review

Impaired Iron Status in Aging Research

Journal

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 13, Issue 2, Pages 2368-2386

Publisher

MDPI AG
DOI: 10.3390/ijms13022368

Keywords

labile iron; iron accumulation; oxidative damage; mitochondrial dysfunction; aging

Funding

  1. NIH [NIH AG17994, NIH DK080706]
  2. American Heart Association [09POST2060112]
  3. University of Florida Institute on Aging and Claude D. Pepper Older Americans Independence Center [1 P30AG028740]

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Aging is associated with disturbances in iron metabolism and storage. During the last decade, remarkable progress has been made toward understanding their cellular and molecular mechanisms in aging and age-associated diseases using both cultured cells and animal models. The field has moved beyond descriptive studies to potential intervention studies focusing on iron chelation and removal. However, some findings remain controversial and inconsistent. This review summarizes important features of iron dyshomeostasis in aging research with a particular emphasis on current knowledge of the mechanisms underlying age-associated disorders in rodent models.

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