4.1 Article

Green tea consumption and serum malondialdehyde-modified LDL concentrations in healthy subjects

Journal

JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION
Volume 24, Issue 5, Pages 342-346

Publisher

ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD
DOI: 10.1080/07315724.2005.10719483

Keywords

green tea; LDL oxidation; in vivo

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Objective: Green tea was shown to inhibit LDL oxidation, platelet aggregation, and matrix metalloproteinases (MMPs) activities in vitro. We tried to elucidate whether or not green tea consumption may have these effects in vivo, which may be protective against atherosclerotic disease, Methods: We measured serum malondialdehyde-modified LDI, (MDA-LDL) concentrations and urine 8-epi-prostaglandin (PG) F-2 alpha in 22 healthy mate nonsmokers. They drank 7 cups/day of water for 2 weeks and drank 7 cups/day of green tea for the next 2 weeks. Regarding platelet aggregation, plasma thromboxane B-2 (TXB2) and 6-keto-PGF(1 alpha) concentrations and ex vivo platelet aggregation Acre evaluated, Plasma MMP-2 and -9 concentrations were also measured. Results: Of the 22 subjects, 20 had been in the habit of drinking green tea before the stud's Plasma catechins concentrations significantly decreased at the end of the water period and then increased at the end of the green tea period. Although no change in plasma LDL-cholesterol concentrations (110 +/- 33 vs, 113 +/- 28 mg/dL. p NS) was found, MDA-LDL concentrations (84 +/- 45 vs. 76 +/- 40 IU/L, p < 0.05) and the ratio of MDA-LDL/LDL-cholesterol (0.74 +/- 0.21 vs. 0.65 +/- 0.20, p < 0.02) significantly decreased at the end of the green tea period. However. no significant changes were observed in urine 8-epi-PGF(2 alpha) concentrations. in platelet aggregation, nor in plasma TXB2, 6-keto-PGF(1 alpha) or MMP concentrations. Conclusion: Daily consumption of green tea decreased serum MDA-LDL. concentrations, but it had no significant effects on platelet aggregation. platelet TX production or plasma MMPs concentrations, Our results suggest that green tea consumption may inhibit LDL oxidation in vivo.

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