3 research outputs found
Green tea polyphenols upregulate the Nrf2 signaling pathway and suppress oxidative stress and inflammation markers in D-galactose-induced liver aging in mice
The beneficial effects of green tea polyphenols (GTPs) on D-galactose (D-Gal)-induced
liver aging in male Kunming mice were investigated. For this purpose, 40 adult
male Kunming mice were divided into four groups. All animals, except for the
normal control and GTPs control, were intraperitoneally injected with D-galactose
(D-Gal; 300 mg/kg/day for 5 days a week) for 12 consecutive weeks, and the
D-Gal-treated mice were allowed free access to 0.05% GTPs (w/w) diet or normal
diet for 12 consecutive weeks. Results showed that GTP administration improved
the liver index and decreased transaminases and total bilirubin levels. Furthermore,
GTPs significantly increased hepatic glutathione and total antioxidant levels, and the
activities of superoxide dismutase, catalase, and glutathione S-transferase (GST).
Furthermore, GTPs downregulated 8-hydroxy-2-deoxyguanosine, advanced glycation
end products, and hepatic oxidative stress markers, such as malondialdehyde
and nitric oxide. Additionally, GTPs abrogated dysregulation in hepatic Kelch-like
ECH-associated protein 1 and nuclear factor erythroid 2-related factor 2 (Nrf2)
and its downstream target gene expression [heme oxygenase 1, NAD(P)H:quinone
oxidoreductase 1, and GST] and inhibited tumor necrosis factor-α, transforming growth
factor-β, and interleukin (IL)-1β and IL-6 in the liver of treated mice. Finally, GTPs
effectively attenuated D-Gal-induced edema, vacuole formation, and inflammatory cell
infiltration. In conclusion, GTPs showed antioxidant and anti-inflammatory properties in
D-Gal-induced aging mice, and may be considered a natural alternative to the effects of
hepatic aging
Analytical Strategy Coupled with Response Surface Methodology To Maximize the Extraction of Antioxidants from Ternary Mixtures of Green, Yellow, and Red Teas (Camellia sinensis var. <i>sinensis</i>)
This work aimed at using a simplex-centroid
design to model the
effects of green, yellow, and red tea mixtures (Camellia
sinensis var. <i>sinensis</i>) on metal
chelation activity, phenolic composition, antioxidant activity, and
instrumental taste profile. The regression models that described the
extraction of flavan-3-ols, <i>o</i>-diphenols, total phenolic
compounds (TPC), free radical scavenging activity toward 2,2-diphenyl-1-picrylhydrazyl
radical (DPPH), cupric ion reducing antioxidant activity (CUPRAC),
and ferric reducing antioxidant power (FRAP) were significant, and
data were fit satisfactorily (<i>R</i><sup>2</sup> >
80%).
A mixture of green and red teas had a synergism in CUPRAC and TPC,
whereas a mixture of yellow and red teas had a positive effect on
CUPRAC and DPPH. An optimization was performed to maximize the antioxidant
activity and flavan-3-ol content and to render a tea with mild bitterness,
and results showed that a mixture of 14.81% green, 56.86% yellow,
and 28.33% red teas would be the most suitable combination of factors
From the forest to the plate – hemicelluloses, galactoglucomannan, glucuronoxylan, and phenolic-rich extracts from unconventional sources as functional food ingredients
This study aimed to characterise pressurised hot water (PHW) extracts from
nonconventional sources of functional carbohydrates and phenolic compounds in terms of antioxidant capacity, antiviral activity, toxicity, and human erythrocytes’ protection antidiabetic potential. PHW extracts of Norway spruce bark (E1 + E2) and Birch sawdust (E3 + E4) contained mostly galactoglucomannan and glucuronoxylan. In contrast, samples E5 to E9 PHW extracted from Norway spruce, and Scots pine bark are rich sources of phenolic compounds. Overall, phenolic-rich extracts presented the highest inhibition of α-amylase and α-glucosidase and protection against stable non-enveloped enteroviruses. Additionally, all extracts protected human erythrocytes from hemolysis.
Cell-based experiments using human cell lines (IMR90 and A549) showed extracts’ non-toxic in vitro profile. Considering the relative toxicological safety of extracts from these unconventional sources, functional carbohydrates and polyphenol-rich extracts can be obtained and further used in food model