New Reaction Pathways of Dopamine under Oxidative Stress Conditions: Nonenzymatic Iron-Assisted Conversion to Norepinephrine and the Neurotoxins 6-Hydroxydopamine and 6,7-Dihydroxytetrahydroisoquinoline

Aerial oxidation of dopamine at concentrations as low as 50 muM. in the presence of ferrou-s ions in phosphate buffer (pH 7.4) led in the early stages (6-8 h) to the formation of the quinone of the neurotoxin 6-hydroxydopamine, 2, followed (24 h) by a complex product pattern comprising- main components norepinephrine (5), 3,4-dihydroxybenzaldehyde (4), and the neurotoxic alkaloid 6,7-dihydroxy-l,2,3,4-tetrahydroisoqumohne (3J. Product formation required the assistance of metal ions such as Mn(ll), Zn(ll), and iron, in either the ferrous or ferric form. Product yields were shown to vary linearly with iron and dopamine concentration in the early phases of the reaction (2 h). Biologically relevant antioxidants, like glutathionc and ascorbate, and metal chelators, e.g., 2,2ʹ-bipyridyl, inhibited dopamine conversion to products 2-5, but not substrate consumption, while hydroxyl radical scavengers such as DMSO and mannitol did not alter the course of the reaction. On the contrary, mannitol increased product yields, an effect seen for other monosaccharides. Catalase exhibited a significant inhibitory effect particularly on the formation of 3 and 4. By using ^02, evidence was obtained for •incorporation of the label into the carbonyl oxygen of 4, but not into the hydroxyl group of 5. Or the basis of these and other results, a complete mechanistic picture of the oxidation is drawn involving conversion of dopairnne to the corresponding o-quinone and its quinonemethide •Lautomer with concomitant reduction of 02 to H^O^. Nucleophilic attack by 1120 to the quinonemethide gives rise to 5, while H^Og addition leads to benzaldebyde 4 via a ^-aminohydroperoxide intermediate. This latter reaction path also gives formaldehyde which yields the isoquinoline 3 by Pictet-Spengler condensation with dopamine. The quinone 2 results from H^Oa attack at the 6-position of dopamine o-quinone in agreement with previous studies. These results provide an insight into new routes of nonenzymatic conversion of dopamine to :its metabolite norepinephrine and neurotoxic species which may become operative under conditions relevant to neurodegeneration.