Flavonoids are phenolic substances isolated from a wide range of vascular plants, with over 8000 individual compounds known. They act in plants as antioxidants, antimicrobials, photoreceptors, visual attractors, feeding repellants, and for light screening. Many studies have suggested that flavonoids exhibit biological activities, including antiallergenic, antiviral, antiinflammatory, and vasodilating actions. However, most interest has been devoted to the antioxidant activity of flavonoids, which is due to their ability to reduce free radical formation and to scavenge free radicals. The capacity of flavonoids to act as antioxidants in vitro has been the subject of several studies in the past years, and important structure-activity relationships of the antioxidant activity have been established. The antioxidant efficacy of flavonoids in vivo is less documented, presumably because of the limited knowledge on their uptake in humans. Most ingested flavonoids are extensively degraded to various phenolic acids, some of which still possess a radical-scavenging ability. Both the absorbed flavonoids and their metabolites may display an in vivo antioxidant activity, which is evidenced experimentally by the increase of the plasma antioxidant status, the sparing effect on vitamin E of erythrocyte membranes and low-density lipoproteins, and the preservation of erythrocyte membrane polyunsaturated fatty acids. This review presents the current knowledge on structural aspects and in vitro antioxidant capacity of most common flavonoids as well as in vivo antioxidant activity and effects on endogenous antioxidants.

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Commonly used medicinal plant extracts with standardized content of polyphenols were investigated for their total antioxidant activity (TAA). Green tea, oligomeric procyanidins (from grape seed and pine bark), bilberry, and ginkgo exhibited TAA in the range of 5.12−2.57 mM Trolox, thereby indicating a valuable antioxidant capacity. Witch hazel, propolis EPID, artichoke, and hawthorn afforded lower TAA (1.54−0.44 mM Trolox), whereas echinacea, ginseng, passionflower, sweet clover, and eleuthero were rather uneffective (TAA < 0.32 mM Trolox). Excipients normally used to prepare the extracts did not interfere with the assay, and a good correlation between the content of polyphenols and the TAA was assessed. The measured TAA was higher than those calculated from the content and antioxidant potential of specific components, as exemplified for green tea and ginkgo extracts. This may be attributed to the presence in these extracts of other substances with antioxidant capacity. On the other hand, some components (such as ginkgolides in ginkgo extract) insensitive to the TAA assay played an important antioxidant role in vivo. These results suggest that TAA determination is of interest for a comparative evaluation of in vitro antioxidant potential, but it needs to be combined with in vivo data for adequate assessment of the antioxidant capacity of medicinal plant extracts. Keywords: Medicinal plants; polyphenols; total antioxidant activity; total radical-trapping antioxidant parameter

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Stevia rebaudiana standardized extracts (SSEs) are used as natural sweeteners or dietary supplements in different countries for their content of stevioside or rebaudioside A. These compounds possess up to 250 times the sweetness intensity of sucrose, and they are noncaloric and noncariogenic sweeteners. The aim of this study was to investigate the in vitro transformation of stevioside and rebaudioside A after incubation with human microflora, the influence of these sweeteners on human microbial fecal community and which specific groups metabolize preferentially stevioside and rebaudioside A. The experiments were carried out under strict anaerobic conditions in batch cultures inoculated with mixed fecal bacteria from volunteers. The hydrolysis was monitored by HPLC coupled to photodiode array and mass spectrometric detectors. Isolated bacterial strains from fecal materials incubated in selective broths were added to stevioside and rebaudioside A. These sweeteners were completely hydrolyzed to their aglycon steviol in 10 and 24 h, respectively. Interestingly, the human intestinal microflora was not able to degrade steviol. Furthermore, stevioside and rebaudioside A did not significantly influence the composition of fecal cultures; among the selected intestinal groups, bacteroides were the most efficient in hydrolyzing Stevia sweeteners to steviol.