Various drugs and other chemicals, such as organic amines, metals, pol
ycyclic aromatic hydrocarbons, etc., are bound to melanin and retained
in pigmented tissues for long periods. The physiological significance
of the binding is not evident, but it has been suggested that the mel
anin protects the pigmented cells and adjacent tissues by adsorbing po
tentially harmful substances, which then are slowly released in nontox
ic concentrations. Long-term exposure, on the other hand, may build up
high levels of noxious chemicals, stored on the melanin, which ultima
tely may cause degeneration in the melanin-containing cells, and secon
dary lesions in surrounding tissues. In the eve, e.g., and in the inne
r ear, the pigmented cells are located close to the receptor cells, an
d melanin binding may be an important factor in the development of som
e ocular and inner ear lesions. In the brain, neuromelanin is present
in nerve cells in the extrapyramidal system, and the melanin affinity
of certain neurotoxic agents may be involved in the development of par
kinsonism, and possibly tardive dyskinesia. In recent years, various c
arcinogenic compounds have been found to accumulate selectively in the
pigment cells of experimental animals, and there are many indications
of a connection between the melanin affinity of these agents and the
induction of malignant melanoma.