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Article type: Research Article
Authors: Ramoutar, Ria R. | Brumaghim, Julia L.
Affiliations: Clemson University, Clemson University, SC, USA
Note: [] Corresponding author. E-mail: [email protected]
Abstract: The organosulfur compounds allicin, methionine and methylcysteine protect against metal-mediated oxidative DNA damage, but few studies have determined the antioxidant behaviour of the oxo-sulfur derivatives of these compounds. Gel electrophoresis experiments were performed to determine the ability of MetSO, MeCysSO, MMTS, MePhSO and Me2SO2 to inhibit copper- and iron-mediated DNA damage. Under these conditions, MetSO and MeCysSO significantly inhibit DNA damage, MePhSO and Me2SO2 have no effect and MMTS promotes DNA damage. For iron-mediated DNA damage, significantly less antioxidant or pro-oxidant behaviour is observed for these compounds. To determine whether metal coordination is a mechanism for the antioxidant activity of these oxo-sulfur compounds, UV–vis spectroscopy and gel electrophoresis experiments using [Cu(bipy)2]+ or [Fe(EDTA)]2− as the metal source were also performed. Results of these experiments indicate that metal coordination is a significant factor for their antioxidant activity, but another mechanism also contributes to their antioxidant behaviour.
Keywords: DNA damage inhibition, antioxidant, oxo-sulfur compounds
DOI: 10.1080/10241220802012387
Journal: Main Group Chemistry, vol. 6, no. 3, 4, pp. 143-153, 2007
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