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1.
Food Chem Toxicol ; 39(12): 1205-10, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11696394

ABSTRACT

We examined the antioxidant activity of the following natural phenolic compounds present in food: 3-OH-benzoic acid (3-OH-BA); 4-OH-benzoic acid (4-OH-BA); 2,3-dihydroxybenzoic acid (2,3-diOH-BA); 3,4-dihydroxybenzoic acid (3,4-diOH-BA or protocatechuic acid); ferulic acid; caffeic acid; and 2-coumaric, 3-coumaric and 4-coumaric acids. We measured the inhibitory effect of these compounds on iron-dependent oxidative DNA damage in vitro [incubating herring sperm DNA with Fe(III)/GSH] or using cumene hydroperoxide (CumOOH) as a free-radical generating system; we also studied the interaction of these phenols with Fe(II) or Fe(III) spectrophotometrically. Among the tested compounds, 2,3-diOH-BA, 3,4-diOH-BA and caffeic acid interacted with Fe(II) and showed a potent inhibitory effect on iron-induced oxidative DNA damage. CumOOH-induced DNA oxidation was not modified by these compounds. On the contrary, 2-coumaric, 3-coumaric and 4-coumaric acids did not interact with iron but protected against oxidative DNA damage induced by Fe(III)/GSH and by CumOOH, indicating a direct free-radical scavenging activity of these compounds in both systems. The IC(50)+/-S.E.M. of the three coumaric acids against CumOOH-induced DNA oxidation was 44.2+/-2.0, 54.7+/-2.0 and 33.1+/-1.0 microM, respectively. On the contrary, 3-OH-BA and 4-OH-BA did not have scavenging activity and 3-OH-BA actually enhanced oxidative DNA damage. In conclusion, some natural phenolic acids, commonly present in food, have interesting protective activity against DNA oxidation in vitro and deserve further consideration as effective antioxidants in vivo.


Subject(s)
Antioxidants/pharmacology , DNA Damage/drug effects , Free Radical Scavengers/metabolism , Hydroxybenzoates/pharmacology , Animals , Antioxidants/metabolism , Benzoates/metabolism , Benzoates/pharmacology , Caffeic Acids/metabolism , Caffeic Acids/pharmacology , Coumaric Acids/metabolism , Coumaric Acids/pharmacology , Fishes , Hydroxybenzoates/metabolism , Inhibitory Concentration 50 , Iron , Male , Oxidation-Reduction , Semen
2.
Eur J Nutr ; 40(2): 74-7, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11518202

ABSTRACT

BACKGROUND & AIMS: Red wine polyphenols inhibit chemically-induced oxidative DNA damage in vivo in experimental animals through a mechanism which is still unclear. On this basis, we tried to clarify the mechanisms of inhibition of DNA oxidation in vitro by wine extracts containing monomeric and polymeric phenols (WE) and monomer-free complex polyphenols and tannins (WCPT) from red wine. METHODS: Oxidative DNA damage was induced by incubating DNA with GSH/Fe3+ or cumene hydroperoxide (CumOOH) in vitro and using 8-OH-2-deoxyguanosine (8-OHdG) levels as a measure of DNA oxidation. Levels of 8-OHdG were determined by HPLC coupled with electrochemical detector (ESA). RESULTS AND CONCLUSIONS: WCPT and WE, at microM concentrations, reduced concentration-dependently oxidative DNA damage induced by GSH/Fe3+. WCPT and WE also reduced DNA oxidation by CumOOH. In conclusion, complex polyphenols and tannin extracts from red wine, with or without small molecular phenols, prevent oxidative DNA damage through a dual mechanism, iron binding and direct free radical scavenging.


Subject(s)
Antioxidants/pharmacology , DNA Damage/drug effects , Flavonoids , Free Radical Scavengers/metabolism , Phenols/pharmacology , Polymers/pharmacology , Tannins/pharmacology , Wine , Animals , Antioxidants/metabolism , Chromatography, High Pressure Liquid , Fishes , In Vitro Techniques , Iron , Iron Chelating Agents/pharmacology , Male , Oxidation-Reduction , Phenols/metabolism , Polymers/metabolism , Polyphenols , Semen , Tannins/metabolism
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