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CONSEQUENCES OF IRON OVERLOAD

[Ref 39]

Iron free radicals and diseases (human)

Iron is supposed to play a key role, especially by catalyzing the formation of OH. radicals* in some
pathologic conditions:

1 Coronary heart disease
2 Ischaemia reperfusion damage
3 Rheumatoid arthritis
4 Certain types of cancer

...where iron possibly may stimulate lipid peroxidation and destruction of proteins and DNA.

https://studmed.uio.no/elaring/lcms16/ernaeringslaere/iron/illustrations/the_fenton_rxn.JPG

Normal conditions

During normal (non-pathologic) conditions the "oxidative stress" is supposed to be limited. This is due to natural mechanisms of protection which remove free radicals.

INTRACELLULAR ANTIOXIDANTS, e.g.:

  • Superoxide dismutase
  • Glutathione peroxidase
  • Catalase
  • Vitamin E
  • Vitamin C

EXTRACELLULAR ANTIOXIDANTS, e.g.:

  • Vitamin E
  • Vitamin C
  • Ceruloplasmin (copper ions)
  • Albumin (copper ions)
  • Transferrin (iron ions)
  • Haemopexin (haem)
  • Haptoglobin (haem proteins)

"EVERYTHING IN MODERATION"

Most of the ferric complexes react more slowly (if at all) with H2O2 than the ferrous complexes.

Reducing substances stimulate the Fenton reaction.
This may happen with vitamin C (ascorbic acid):

  • Fe(III) + ascorbate --> Fe(II) + semidehydroascorbate,

    Fe(II) joins the Fenton reaction.

Mixtures of iron salts, ascorbic acid and H2O2 may thus be good
sources for OH. radicals.

In other words, vitamin C in reasonable amounts acts as an antioxidant; in megadoses (> 500 mg/d) vitamin C may be damaging by acting as a prooxidant, especially in individuals with iron overload.

[Ref 40]