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The consumption of fruit juice rich in flavonoids increases plasma antioxidant status

Published online by Cambridge University Press:  28 January 2009

Chutamat Niwat
Affiliation:
University of Reading, Reading, UK
Trevor George
Affiliation:
University of Reading, Reading, UK
Michael Gordon
Affiliation:
University of Reading, Reading, UK
Julie Lovegrove
Affiliation:
University of Reading, Reading, UK
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2009

Fruits and vegetables rich in flavonoids have been related to the reduction in the incidence of CVD in several epidemiological studies(Reference Halliwell, Joseph and Jenner1). Flavonoids are a group of phenolic compounds with strong antioxidant activity. Thus, the protective effects of the flavonoids could be a result of their ability to scavenge reactive oxygen and nitrogen species, which are formed during intracellular oxidative stress(Reference Rohn, Rawel and Kroll2). However, postprandial effects on antioxidant status after consumption of fruits and juices are controversial(Reference Dragsted, Pederson and Hermetter3, Reference Mazza, Kay, Cottrell and Holub4). In addition, very little is known about the amount of flavonoids absorbed from the diet and the reliability of plasma biomarkers(Reference Erdman, Balentine and Arab5). Consequently, the aim of the present study was to investigate the beneficial effects of an acute intervention with flavonoid-rich juices on markers of oxidative stress and cardiovascular risk factors.

A single-blind randomized postprandial study was performed in a group of twenty-four healthy free-living volunteers (twenty males and four females) with an age range of 28–64 years and a low habitual fruit and vegetable intake (less than five portions per d). Volunteers were asked to consume a low-flavonoid diet for 5 d before the study day and fast overnight the day before the study. The volunteers were randomly allocated to consume either 400 ml flavonoid-rich juice (providing 768 mg total phenolics (gallic acid equivalents (GAE)) including 142.2 μg anthocyanins) or 400 ml control juice, which had a low content of flavonoids (44 mg total phenolics (GAE)) but had the same sugar content. Two blood samples were taken at baseline and then fourteen subsequent samples at time intervals after the ingestion of the juice and throughout the study day for 8 h. After an interval of 1 month they were asked to repeat the process with the second type of juice.

Plasma antioxidant status was measured before and up to 8 h after fruit-juice consumption by the ferric-reducing antioxidant potential (FRAP) assay(Reference Benzie and Strain6), the Trolox equivalent antioxidant capacity (TEAC) assay(Reference Re, Pellegrini, Proteggente, Pannala, Yang and Rice-Evans7) and the oxygen radical absorbance capacity (ORAC) assay(Reference Cao and Prior8). Plasma vitamin C, uric acid and total nitrates were also determined in the collected blood samples. It was observed that plasma FRAP increased significantly by 7.91% after ingestion of the flavonoid-rich juice compared with the flavonoid-poor juice (P=0.031). This finding was confirmed by the TEAC and ORAC assays, which showed significant increases, by 8.89% (P=0.026) and 13.5% (P=0.015) respectively. In addition, plasma total nitrate and vitamin C increased significantly by 21.8% (P=0.001) and 34.9% (P=0.013) respectively. Correlations between these measures of antioxidant status and plasma levels of vitamin C, uric acid and total nitrate were investigated. It was observed that only FRAP values correlated significantly and positively with plasma nitrate (r 2 0.472, P=0.02). However, the correlation between plasma vitamin C and uric acid with antioxidant status will be re-investigated when data from all twenty-four volunteers are available.

It was concluded that ingestion of a flavonoid-rich fruit juice significantly increased postprandial antioxidant status in a group of healthy volunteers.

Funding provided by Unilever Bestfoods, The Royal Thai Government and University of Reading Endowment Trust Fund is gratefully acknowledged.

References

1. Halliwell, B, Joseph, R & Jenner, A (2005) Am J Clin Nutr 81, Suppl., 268S276S.CrossRefGoogle Scholar
2. Rohn, S, Rawel, HM & Kroll, J (2004) J Agric Food Chem 52, 47254729.CrossRefGoogle Scholar
3. Dragsted, LO, Pederson, A, Hermetter, A et al. (2004) Am J Clin Nutr 79, 10601072.CrossRefGoogle Scholar
4. Mazza, G, Kay, CD, Cottrell, T & Holub, BJ (2002) J Agri Food Chem 50, 77317737.CrossRefGoogle Scholar
5. Erdman, JW, Balentine, D, Arab, L et al. (2007) J Nutr 137, 718S737S.CrossRefGoogle Scholar
6. Benzie, IFF & Strain, JJ (1996) Anal Biochem 239, 7076.CrossRefGoogle Scholar
7. Re, R, Pellegrini, N, Proteggente, A, Pannala, A, Yang, M & Rice-Evans, C (2000) Free Rad Biol Med 26, 12311237.CrossRefGoogle Scholar
8. Cao, GH & Prior, RL (1999) Methods Enzymol 299, 5062.CrossRefGoogle Scholar