dc.creator | Pardo-Andreu, Gilberto Lázaro | |
dc.creator | Delgado, René | |
dc.creator | Núñez-Sellés, Alberto J | |
dc.creator | Vercesi, Anibal E | |
dc.date | 2006-Feb | |
dc.date | 2015-11-27T13:06:17Z | |
dc.date | 2015-11-27T13:06:17Z | |
dc.date.accessioned | 2018-03-29T01:04:16Z | |
dc.date.available | 2018-03-29T01:04:16Z | |
dc.identifier | Phytotherapy Research : Ptr. v. 20, n. 2, p. 120-4, 2006-Feb. | |
dc.identifier | 0951-418X | |
dc.identifier | 10.1002/ptr.1813 | |
dc.identifier | http://www.ncbi.nlm.nih.gov/pubmed/16444664 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/197144 | |
dc.identifier | 16444664 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1297377 | |
dc.description | Vimang is an aqueous extract of selected species of Mangifera indica L, used in Cuba as a nutritional antioxidant supplement. Many in vitro and in vivo models of oxidative stress have been used to elucidate the antioxidant mechanisms of this extract. To further characterize the mechanism of Vimang action, its effect on the degradation of 2-deoxyribose induced by Fe (III)-EDTA plus ascorbate or plus hypoxanthine/xanthine oxidase was studied. Vimang was shown to be a potent inhibitor of 2-deoxyribose degradation mediated by Fe (III)-EDTA plus ascorbate or superoxide (O2-). The results revealed that Vimang, at concentrations higher than 50 microM mangiferin equivalent, was equally effective in preventing degradation of both 15 mM and 1.5 mM 2-deoxyribose. At a fixed Fe (III) concentration, increasing the concentration of ligands (either EDTA or citrate) caused a significant reduction in the protective effects of Vimang. When ascorbate was replaced by O2- (formed by hypoxanthine and xanthine oxidase) the protective efficiency of Vimang was also inversely related to EDTA concentration. The results strongly indicate that Vimang does not block 2-deoxyribose degradation by simply trapping *OH radicals. Rather, Vimang seems to act as an antioxidant by complexing iron ions, rendering them inactive or poorly active in the Fenton reaction. | |
dc.description | 20 | |
dc.description | 120-4 | |
dc.language | eng | |
dc.relation | Phytotherapy Research : Ptr | |
dc.relation | Phytother Res | |
dc.rights | fechado | |
dc.rights | Copyright 2006 John Wiley & Sons, Ltd. | |
dc.source | PubMed | |
dc.subject | Ascorbic Acid | |
dc.subject | Deoxyribose | |
dc.subject | Edetic Acid | |
dc.subject | Ferric Compounds | |
dc.subject | Mangifera | |
dc.subject | Oxidation-reduction | |
dc.subject | Oxidative Stress | |
dc.subject | Plant Extracts | |
dc.subject | Superoxides | |
dc.title | Mangifera Indica L. Extract (vimang) Inhibits 2-deoxyribose Damage Induced By Fe (iii) Plus Ascorbate. | |
dc.type | Artículos de revistas | |