REDUCTION OF 13-HYDROPEROXY-9,11-OCTADECADIENOIC ACID BY DOPAMINE-MELANIN

Citation
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
Citations number
39
Categorie Soggetti
Biology,Biophysics
ISSN journal
0006291X
Volume
244
Issue
3
Year of publication
1998
Pages
781 - 784
Database
ISI
SICI code
0006-291X(1998)244:3<781:RO1ABD>2.0.ZU;2-M
Abstract
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.