Antioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxytyrosol.
dc.contributor.author | Aeschbach, R | |
dc.contributor.author | Löliger, J | |
dc.contributor.author | Scott, B C | |
dc.contributor.author | Murcia, A | |
dc.contributor.author | Butler, John | |
dc.contributor.author | Halliwell, B | |
dc.contributor.author | Aruoma, O I | |
dc.date.accessioned | 2010-04-20T16:14:23Z | |
dc.date.available | 2010-04-20T16:14:23Z | |
dc.date.issued | 1994-01 | |
dc.identifier.citation | Antioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxytyrosol. 1994, 32 (1):31-6 Food Chem. Toxicol. | en |
dc.identifier.issn | 0278-6915 | |
dc.identifier.pmid | 7510659 | |
dc.identifier.doi | 10.1016/0278-6915(84)90033-4 | |
dc.identifier.uri | http://hdl.handle.net/10541/96924 | |
dc.description.abstract | Antioxidants 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.iso | en | en |
dc.subject.mesh | Antioxidants | |
dc.subject.mesh | Ascorbic Acid | |
dc.subject.mesh | Bleomycin | |
dc.subject.mesh | Catechols | |
dc.subject.mesh | DNA Damage | |
dc.subject.mesh | Deoxyribose | |
dc.subject.mesh | Fatty Alcohols | |
dc.subject.mesh | Ferric Compounds | |
dc.subject.mesh | Food Preservation | |
dc.subject.mesh | Guaiacol | |
dc.subject.mesh | Hydroxyl Radical | |
dc.subject.mesh | Lipid Peroxidation | |
dc.subject.mesh | Liposomes | |
dc.subject.mesh | Monoterpenes | |
dc.subject.mesh | Phenylethyl Alcohol | |
dc.subject.mesh | Pulse Radiolysis | |
dc.subject.mesh | Terpenes | |
dc.subject.mesh | Thymol | |
dc.title | Antioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxytyrosol. | en |
dc.type | Article | en |
dc.contributor.department | Centre de Recherche, Nestec SA, Vers-Chez-les-Blanc, Lausanne, Switzerland. | en |
dc.identifier.journal | Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association | en |
html.description.abstract | Antioxidants 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. |