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Reaction mechanism of melatonin oxidation by reactive oxygen species in vitro

Authors

  • Dominique Bonnefont-Rousselot,

    1. EA 4466, Département de Biologie Expérimentale, Métabolique et Clinique, Faculté des Sciences Pharmaceutiques et Biologiques, Université Paris Descartes, Paris, France
    2. Service de Biochimie Métabolique, Groupe Hospitalier Pitié-Salpêtrière (AP-HP), Paris, France
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  • Fabrice Collin,

    1. UFR Biomédicale des Saints-Pères, Université Paris Descartes, Paris, France
    2. IRD UMR 152, Université Paul Sabatier, Toulouse, France
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  • Daniel Jore,

    1. UFR Biomédicale des Saints-Pères, Université Paris Descartes, Paris, France
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  • Monique Gardès-Albert

    1. UFR Biomédicale des Saints-Pères, Université Paris Descartes, Paris, France
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Address reprint requests to Dominique Bonnefont-Rousselot, EA 4466, Département de Biologie Expérimentale, Métabolique et Clinique, Faculté des Sciences Pharmaceutiques et Biologiques, Université Paris Descartes, 4 avenue de l’Observatoire, 75006 Paris, France.
E-mail: dominique.bonnefont-rousselot@parisdescartes.fr

Abstract

Abstract:  Melatonin (N-acetyl-5-hydroxytryptamine) is a pineal hormone widely known for its antioxidant properties, both in vivo and by direct capture of free radicals in vitro. Although some metabolites and oxidation products of melatonin have been identified, the molecular mechanism by which melatonin exerts its antioxidant properties has not been totally unravelled. This study investigated the reaction mechanism of oxidation of melatonin by radio-induced reactive oxygen species, generated by gamma radiolysis of water for aqueous solutions of melatonin (from 20 to 200 μm), in the presence or absence of molecular oxygen. The hydroxyl radical was found to be the unique species able to initiate the oxidation process, leading to three main products, e.g. N1-acetyl-N2-formyl-5-methoxykynurenin (AFMK), N1-acetyl-5-methoxykynurenin (AMK) and hydroxymelatonin (HO-MLT). The generation of AFMK and HO-MLT strongly depended on the presence of molecular oxygen in solution: AFMK was the major product in aerated solutions (84%), whereas HO-MLT was favoured in the absence of oxygen (86%). Concentrations of AMK remained quite low, and AMK was proposed to result from a chemical hydrolysis of AFMK in solution. A K-value of 1.1 × 10−4 was calculated for this equilibrium. Both hydrogen peroxide and superoxide dismutase had no effect on the radio-induced oxidation of melatonin, in good accordance for the second case with the poor reactivity of the superoxide anion towards melatonin. Finally, a reaction mechanism was proposed for the oxidation of melatonin in vitro.

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