News Release

Aging-US: Iron: an underrated factor in aging

Iron, which can then react with and damage cellular structures, which in turn can lead to organ damage and the deterioration associated with aging

Peer-Reviewed Publication

Impact Journals LLC

Aging-US published "Iron: an underrated factor in aging" which reported that iron is an essential element for virtually all living organisms, but its reactivity also makes it potentially harmful. Blocking iron absorption through drugs or natural products extends lifespan.

Dr. Dennis Mangan from MTOR LLC in Bakersfield California said, "All life forms require the element iron as a constituent of their biochemical systems, iron being used in producing ATP in mitochondria, in cytochromes and hemoglobin, and in many other uses."

Iron is essential for organismal growth and maintenance, so all life, from bacteria and algae to mammals, have developed the means to collect and store iron from their environments; this centrality of iron for all life suggests that iron may be involved in aging.

Most organisms, including humans, have no systematic means of ridding themselves of excess iron. A problem that organisms face in the use of iron in biological systems is protecting cells from iron damage. The very property of iron that makes it useful, its ability to accept or donate electrons, also gives it the ability to damage molecules and organelles via the Fenton reaction, in which iron reacts with hydrogen peroxide, leading to the formation of the highly reactive and toxic free radical, hydroxyl.

In theory, these storage proteins should be enough to protect organelles and macromolecules from iron’s reactivity, but in practice another process becomes perhaps more important, and that is iron dysregulation. Storage proteins such as ferritin can themselves be damaged, leading to «leakage» of free iron, which can then react with and damage cellular structures, which in turn can lead to organ damage and the deterioration associated with aging.

The Mangan Research Team concluded in their Aging-US Research Output, "iron satisfies many of the conditions we might look for in a universally pro-aging substance. It accumulates with age; it is associated with many age-related diseases such as cardiovascular disease, cancer, and Alzheimer’s disease; it catalyzes the formation of cellular junk molecules and helps to prevent their turnover; removal of iron from plasma may be rejuvenating; and people with lower levels of body iron – blood donors – have a lower mortality rate.

Iron is intimately associated with aging, and control of body iron stores may be an important way to extend human lifespan."

Full Text - https://www.aging-us.com/article/203612/text

Correspondence to: Dennis Mangan email: pdmangan@outlook.com

Keywords: ironagingoxidative stresscalorie restrictionplasma dilution

About Aging-US

Launched in 2009, Aging-US publishes papers of general interest and biological significance in all fields of aging research as well as topics beyond traditional gerontology, including, but not limited to, cellular and molecular biology, human age-related diseases, pathology in model organisms, cancer, signal transduction pathways (e.g., p53, sirtuins, and PI-3K/AKT/mTOR among others), and approaches to modulating these signaling pathways.

To learn more about Aging-US, please visit http://www.Aging-US.com or connect with @AgingJrnl

Aging-US is published by Impact Journals, LLC please visit http://www.ImpactJournals.com or connect with @ImpactJrnls

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FEATURED NOBEL ARTICLES

  • Elizabeth Blackburn, a member of the Editorial Board of Aging, won the Nobel Prize in Physiology or Medicine 2009, while being a member of the board. Elizabeth Blackburn co-authored a paper published in the first (inaugural) issue of Aging.

  • Andrew V. Schally, Nobel Prize Laureate, published his paper in Aging.

  • Shinya Yamanaka won the Nobel Prize in Physiology and Medicine 2012. Shinya Yamanaka co-authored a paperpublished in Aging.

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