Research Article
Effects of olive oil polyphenols on erythrocyte oxidative damage
Article first published online: 2 APR 2009
DOI: 10.1002/mnfr.200800276
Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Molecular Nutrition & Food Research
Special Issue: Arsenic
Volume 53, Issue 5, pages 609–616, May 2009
Additional Information
How to Cite
Paiva-Martins, F., Fernandes, J., Rocha, S., Nascimento, H., Vitorino, R., Amado, F., Borges, F., Belo, L. and Santos-Silva, A. (2009), Effects of olive oil polyphenols on erythrocyte oxidative damage. Molecular Nutrition & Food Research, 53: 609–616. doi: 10.1002/mnfr.200800276
Publication History
- Issue published online: 7 MAY 2009
- Article first published online: 2 APR 2009
- Manuscript Accepted: 15 SEP 2008
- Manuscript Revised: 22 AUG 2008
- Manuscript Received: 3 JUL 2008
- Abstract
- References
- Cited By
Keywords:
- Erythrocytes;
- Hydroxytyrosol;
- Olea europaea;
- Olive oil;
- Polyphenols
Abstract
Many studies have investigated the protective effects of oleuropein and hydroxytyrosol against cell injury, but few have investigated the protective effects of oleuropein aglycones 3,4-dihydroxyphenylethanol-elenolic acid (3,4-DHPEA-EA) and 3,4-dihydroxyphenylethanol-elenolic acid dialdehyde (3,4-DHPEA-EDA). The present work studied and compared the capacity of these four compounds, found at high concentrations in olive oil, to protect red blood cells (RBCs) from oxidative injury. The in vitro oxidative stress of RBCs was induced by the water-soluble radical initiator 2,2′-azo-bis(2-amidinopropane) dihydrochloride. RBC changes were evaluated either by optical microscopy or by the amount of hemolysis. All compounds were shown to significantly protect RBCs from oxidative damage in a dose-dependent manner. The order of activity at 20 μM was: 3,4-DHPEA-EDA > hydroxytyrosol > oleuropein > 3,4-DHPEA-EA. Even at 3 μM, 3,4-DHPEA-EDA and hydroxytyrosol still had an important protective activity. However, deleterious morphological RBC changes were much more evident in the presence of hydroxytyrosol than with 3,4-DHPEA-EDA. For the first time it was demonstrated that 3,4-DHPEA-EDA, one of most important olive oil polyphenols, may play a noteworthy protective role against ROS-induced oxidative injury in human cells since lower doses of this compound were needed to protect RBCs in vitro from oxidative mediated hemolysis.

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