Journal of Agricultural and Food Chemistry · 2001 · 129 citations · 7 references
Life SciencesBotanyPlant SciencesPlant BiochemistryPlant PhysiologyRedox BiochemistryAntioxidant DefenseLipid PeroxidationMedicinal PlantsPhenolic Compound AnalysisRadical ReactionsReactive Oxygen SpeciesAntioxidant Activity AssaysAntioxidant Natural ProductsAntioxidant PropertiesFenton ReactionFree Radical ScavengingNatural AntioxidantsPercolationPhenolic Compounds
In an effort to discover new antioxidant natural compounds, seven plants that grow in France (most of them in the Limousin countryside) were screened. Among these plants, was the extensively studied Vitis vinifera as reference. For each plant, sequential percolation was realized with five solvents of increasing polarities (hexane, chloroform, ethyl acetate, methanol, and water). Free radical scavenging activities were examined in different systems using electron spin resonance (ESR) spectroscopy. These assays were based on the stable free radical 1,1-diphenyl-2-picrylhydrazyl (DPPH), the hydroxyl radicals generated by a Fenton reaction, and the superoxide radicals generated by the X/XO system. Antiproliferative behavior was studied on B16 melanoma cells. ESR results showed that three plants (Castanea sativa, Filipendula ulmaria, and Betula pendula) possessed, for the most polar fractions (presence of phenolic compounds), high antioxidant activities in comparison with the Vitis vinifera reference. Gentiana lutea was the only one that presented a hydroxyl scavenging activity for the ethyl acetate and chloroform fractions. The antiproliferative test results showed that the same three plants are the most effective, but for the apolar fractions (chloroform and hexane).
7
Antioxidant properties of hydroxy-flavones
Nicole Cotelle, Jean‐Luc Bernier, Jean‐Pierre Catteau et al. · Free Radical Biology and Medicine · 1996 · 703 citations