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dc.contributor.authorAeschbach, R
dc.contributor.authorLöliger, J
dc.contributor.authorScott, B C
dc.contributor.authorMurcia, A
dc.contributor.authorButler, John
dc.contributor.authorHalliwell, B
dc.contributor.authorAruoma, O I
dc.date.accessioned2010-04-20T16:14:23Z
dc.date.available2010-04-20T16:14:23Z
dc.date.issued1994-01
dc.identifier.citationAntioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxytyrosol. 1994, 32 (1):31-6 Food Chem. Toxicol.en
dc.identifier.issn0278-6915
dc.identifier.pmid7510659
dc.identifier.doi10.1016/0278-6915(84)90033-4
dc.identifier.urihttp://hdl.handle.net/10541/96924
dc.description.abstractAntioxidants minimize oxidation of the lipid components in foods. There is an increasing interest in the use of natural and/or synthetic antioxidants in food preservation, but it is important to evaluate such compounds fully for both antioxidant and pro-oxidant properties. The properties of thymol, carvacrol, 6-ginerol, hydroxytyrosol and zingerone were characterized in detail. Thymol, carvacrol, 6-gingerol and hydroxytyrosol decreased peroxidation of phospholipid liposomes in the presence of iron(III) and ascorbate, but zingerone had only a weak inhibitory effect on the system. The compounds were good scavengers of peroxyl radicals (CCl3O2; calculated rate constants > 10(6) M-1 sec-1) generated by pulse radiolysis. Thymol, carvacrol, 6-gingerol and zingerone were not able to accelerate DNA damage in the bleomycin-Fe(III) system. Hydroxytyrosol promoted deoxyribose damage in the deoxyribose assay and also promoted DNA damage in the bleomycin-Fe(III) system. This promotion was inhibited strongly in the deoxyribose assay by the addition of bovine serum albumin to the reaction mixtures. Our data suggest that thymol, carvacrol and 6-gingerol possess useful antioxidant properties and may become important in the search for 'natural' replacements for 'synthetic' antioxidant food additives.
dc.language.isoenen
dc.subject.meshAntioxidants
dc.subject.meshAscorbic Acid
dc.subject.meshBleomycin
dc.subject.meshCatechols
dc.subject.meshDNA Damage
dc.subject.meshDeoxyribose
dc.subject.meshFatty Alcohols
dc.subject.meshFerric Compounds
dc.subject.meshFood Preservation
dc.subject.meshGuaiacol
dc.subject.meshHydroxyl Radical
dc.subject.meshLipid Peroxidation
dc.subject.meshLiposomes
dc.subject.meshMonoterpenes
dc.subject.meshPhenylethyl Alcohol
dc.subject.meshPulse Radiolysis
dc.subject.meshTerpenes
dc.subject.meshThymol
dc.titleAntioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxytyrosol.en
dc.typeArticleen
dc.contributor.departmentCentre de Recherche, Nestec SA, Vers-Chez-les-Blanc, Lausanne, Switzerland.en
dc.identifier.journalFood and chemical toxicology : an international journal published for the British Industrial Biological Research Associationen
html.description.abstractAntioxidants minimize oxidation of the lipid components in foods. There is an increasing interest in the use of natural and/or synthetic antioxidants in food preservation, but it is important to evaluate such compounds fully for both antioxidant and pro-oxidant properties. The properties of thymol, carvacrol, 6-ginerol, hydroxytyrosol and zingerone were characterized in detail. Thymol, carvacrol, 6-gingerol and hydroxytyrosol decreased peroxidation of phospholipid liposomes in the presence of iron(III) and ascorbate, but zingerone had only a weak inhibitory effect on the system. The compounds were good scavengers of peroxyl radicals (CCl3O2; calculated rate constants > 10(6) M-1 sec-1) generated by pulse radiolysis. Thymol, carvacrol, 6-gingerol and zingerone were not able to accelerate DNA damage in the bleomycin-Fe(III) system. Hydroxytyrosol promoted deoxyribose damage in the deoxyribose assay and also promoted DNA damage in the bleomycin-Fe(III) system. This promotion was inhibited strongly in the deoxyribose assay by the addition of bovine serum albumin to the reaction mixtures. Our data suggest that thymol, carvacrol and 6-gingerol possess useful antioxidant properties and may become important in the search for 'natural' replacements for 'synthetic' antioxidant food additives.


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