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Department of Food Science and Microbiology, Division of Human Nutrition, University of Milan, Milan, Italy
1To whom correspondence should be addressed.
Regular tea consumption has been associated with a reduced risk of
cancer. As demonstrated in vitro, green tea contains catechins with
antioxidant properties. We evaluated the effect of the supplementation
of the Jurkat T-cell line with green tea extract on oxidative
damage. Cells grown in medium with or without green tea extract (10
mg/L) were treated with Fe2+ (100 µmol/L)
as an oxidative stimulus for 2 h. Cell membrane lipid peroxidation
was evaluated by fatty acids pattern analysis and malondialdehyde
production in
-linolenic acidloaded cells. Furthermore, oxidative
DNA damage (single strand breaks) was detected in cells by the Comet
assay and quantified as relative tail moment (RTM). Supplementation
with green tea extract significantly decreased malondialdehyde
production (1.6 ± 0.3 vs. 0.6 ± 0.1 nmol/mg protein,
P < 0.05) and DNA damage (0.32 ± 0.07 vs.
0.12 ± 0.04 RTM, P < 0.05) after
Fe2+ oxidative treatment. In control cells, there was no
effect on membrane distribution of (n-3) fatty acids due to
Fe2+ treatment. Cell enrichment with
-linolenic acid
increased total membrane (n-3) fatty acids. However, the oxidative
treatment did not modify the distribution of polyunsaturated fatty
acids. It is likely that the observed protective effects can be
attributed to epigallocatechin gallate, which is present mainly (670
g/kg) in green tea extract; however, we cannot exclude contributions by
other catechins. These data support a protective effect of green tea
against oxidative damage.
KEY WORDS: catechins Jurkat T cells lipid peroxidation DNA damage
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