Iron, as the most abundant
transition metal in the human brain, occurs with uneven distribution. Highest concentration
of iron can be observed in areas associated with motor function (Globus
pallidus, putamen, Substantia nigra) than in other areas of the human
brain. Therefore, the actual role of iron accumulation in brain pathobiology isan active area of investigation nowadays.It is evident that amount of iron in
brain gradually grows with age. Accumulation of iron in basal ganglia is
probably associated with neuronal death leading to Alzheimer disease, Parkinson
disease, epilepsy, Huntington disease, dementia with Lewy bodies, and multiple
sclerosis. It was reported that iron participates in redox reactions, and
catalyzes the formation of reactive oxygen species responsible for oxidative
stress and damaging processes.
Iron in the human brain can be
found mostly in the form of ferritin, hemosiderin (a product of ferritin
breakdown) and other biomineralized oxidohydroxides and oxides such as hematite,
magnetite, and maghemite. Ferritin, as an iron storage nonheme-protein with
diameter up to 12 nm, consist of inorganic core (6 nm) formed of ferrihydrite and
minor portion of magnetite and hematite that is enclosed by two types of
polypeptides. The role of the heavy (Ft-H) form polypeptide coat of ferritin is
to catalyze Fe(II) to Fe(III) ions whereas the light (Ft-L) polypeptide coat
promotes the formation of ferritin iron core.The amount of Ft-H and Ft-L
polypeptide coats changes during ageing and the magnetic properties of ferritin
can also alter.(Read More)

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