K. Stepien et al., REDUCTION OF 13-HYDROPEROXY-9,11-OCTADECADIENOIC ACID BY DOPAMINE-MELANIN, Biochemical and biophysical research communications, 244(3), 1998, pp. 781-784
The effect of dopamine-melanin (DA-melanin), synthetic model of neurom
elanin, on the stability of 13-hydroperoxyoctadecadienoic acid (13-HPO
DE) has been investigated using a reverse-phase high-performance liqui
d chromatography (HPLC) with UV detection. It was found that DA-melani
n effectively accelerated the decomposition of 13-HPODE, both in the a
bsence and in the presence of ferrous ions. The disappearance of 13-HP
ODE was accompanied by the formation of 13-hydroxyoctadecadienoic acid
(13-HODE). The results obtained indicate that DA-melanin is able to r
educe linoleic acid hydroperoxide to its stable hydroxyl derivative. T
he fatty acid hydroperoxide-reducing ability of DA-melanin appears to
play an important role in the antioxidative activity of neuromelanin i
n the process of lipid peroxidation. (C) 1998 Academic Press.