Different antioxidant effects of polyphenols on lipid peroxidation and hydroxyl radicals in the NADPH-, Fe-ascorbate- and Fe-microsomal systems
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
14505792
DOI
10.1016/s0006-2952(03)00425-8
PII: S0006295203004258
Knihovny.cz E-zdroje
- MeSH
- antioxidancia farmakologie MeSH
- fenoly farmakologie MeSH
- flavonoidy * MeSH
- hydroxylový radikál metabolismus MeSH
- jaterní mikrozomy účinky léků metabolismus MeSH
- krysa rodu Rattus MeSH
- kyselina askorbová metabolismus MeSH
- NADP metabolismus MeSH
- oxidace-redukce MeSH
- peroxidace lipidů účinky léků MeSH
- polyfenoly MeSH
- polymery farmakologie MeSH
- železo metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antioxidancia MeSH
- fenoly MeSH
- flavonoidy * MeSH
- hydroxylový radikál MeSH
- kyselina askorbová MeSH
- NADP MeSH
- polyfenoly MeSH
- polymery MeSH
- železo MeSH
Antioxidant and pro-oxidant effects of 14 naturally occurring polyphenols (PP) on rat liver microsomal lipid peroxidation (LP) and hydroxyl radical (*OH) production were studied in NADPH-dependent, 50 microM Fe(2+)-500 microM ascorbate (Fe-AA) or 50 microM Fe(2+) system, respectively. LP determined by the thiobarbituric acid method was inhibited in the NADPH system by flavonols and trans-resveratrol that were more effective than other flavonoids and derivatives of benzoic and cinnamic acid and were mostly more efficient than in the Fe-AA system. Inhibition of LP in the Fe system was higher by one order of magnitude than in the Fe-AA system. *OH production in the NADPH system, measured by formaldehyde production, was decreased by myricetin, fisetin and quercetin, but increased by kaempferol, morin and trans-resveratrol, indicating that z.rad;OH played a minor role in LP, which all of these PP inhibited. None of these PP at up to 40 microM concentration quenched *OH in the Fe-AA system. All tested PP, except trans-resveratrol and gentisic acid, spectrally interacted with Fe(2+) or Fe(3+), indicating formation of complexes or oxidation of PP. In contrast to the NADPH system we found no correlation between Fe(2+) chelation and inhibition of Fe-AA- or Fe-dependent LP indicating that iron chelation did not play a significant role in the two latter systems. It is concluded that the inhibition of LP by PP was apparently due to their hydrogen donating properties rather than chelation of iron.
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