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Scavenging of reactive oxygen species by the plant phenols genistein and oleuropein.
- Source :
-
Luminescence : the journal of biological and chemical luminescence [Luminescence] 2005 Mar-Apr; Vol. 20 (2), pp. 81-9. - Publication Year :
- 2005
-
Abstract
- The plant-derived phenolic compounds genistein and oleuropein are known to exhibit several biological properties, many of which may result from their antioxidant and free radical scavenger activity. In this paper we report the results of a complex study of antioxidant activity of genistein and oleuropein, using electron spin resonance (ESR), chemiluminescence, fluorescence and spectrophotometric techniques. Different reaction systems were applied to study the inhibitory effect of the phenolic compounds studied: (a) the potassium superoxide/18-crown-6 dissolved in DMSO system, which generates superoxide radical (O(2).(-)) and hydrogen peroxide (H(2)O(2)); (b) the Co(II)-EDTA-H(2)O(2) system (the Fenton-like reaction), which generates hydroxyl radical (HO.); (c) 2,2'-azobis(2-amidino-propane)dichloride (AAPH) as the peroxyl radical (ROO.) generator, and the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical test. Results showed that genistein and oleuropein decreased the chemiluminescence sum from the O(2).(-) generating system, an inhibitory effect that was dependent on their concentration. These compounds also reacted with ROO radicals and they showed activity about two-fold greater than the standard Trolox. The antioxidant effects were studied at different concentrations and reflected in protection against the fluorescence decay of beta-phycoerythrin (beta-PE), due to ROO. attack on this protein. Using the Fenton-like reaction and the spin trap agent 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), the phenolic compounds examined were found to inhibit DMPO-.OH radical formation in the range 10-90% at concentrations of 0.1 mmol/L to 2 mmol/L. Furthermore, these compounds also inhibited HO.-dependent deoxyribose degradation; about 20% and 60% inhibitions were observed in the presence of 0.5 mmol/L genistein and oleuropein, respectively. It was also demonstrated that genistein had a weaker DPPH radical scavenging activity than oleuropein. Our results confirm good scavenging activity towards O(2).(-), HO. and ROO. and the antioxidant effect of genistein and oleuropein.<br /> (Copyright (c) 2005 John Wiley & Sons, Ltd.)
- Subjects :
- Antioxidants pharmacology
Dose-Response Relationship, Drug
Electron Spin Resonance Spectroscopy
Fluorescence
Genistein chemistry
Genistein metabolism
Hydrogen Peroxide metabolism
Hydroxyl Radical metabolism
Iridoid Glucosides
Iridoids
Luminescent Measurements
Oxygen metabolism
Pyrans chemistry
Pyrans metabolism
Spin Labels
Spin Trapping
Time Factors
Free Radical Scavengers pharmacology
Genistein pharmacology
Phenols chemistry
Plants chemistry
Pyrans pharmacology
Reactive Oxygen Species metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1522-7235
- Volume :
- 20
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Luminescence : the journal of biological and chemical luminescence
- Publication Type :
- Academic Journal
- Accession number :
- 15803505
- Full Text :
- https://doi.org/10.1002/bio.808