Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-25T03:06:33.407Z Has data issue: false hasContentIssue false

Phenolic acid metabolites as biomarkers for tea- and coffee-derived polyphenol exposure in human subjects

Published online by Cambridge University Press:  09 March 2007

Jonathan M. Hodgson*
Affiliation:
University of Western Australia School of Medicine and Pharmacology and the Western Australian Institute for Medical Research at Royal Perth Hospital, Perth, Western Australia, Australia
Shin Yee Chan
Affiliation:
University of Western Australia School of Medicine and Pharmacology and the Western Australian Institute for Medical Research at Royal Perth Hospital, Perth, Western Australia, Australia
Ian B. Puddey
Affiliation:
University of Western Australia School of Medicine and Pharmacology and the Western Australian Institute for Medical Research at Royal Perth Hospital, Perth, Western Australia, Australia
Amanda Devine
Affiliation:
University of Western Australia School of Medicine and Pharmacology and the Western Australian Institute for Medical Research at QEII Medical Centre, Perth, Western Australia, Australia
Naiyana Wattanapenpaiboon
Affiliation:
The Asia Pacific Health and Nutrition Centre, Monash Asia Institute, Monash University, Clayton, Victoria, Australia
Mark L. Wahlqvist
Affiliation:
The Asia Pacific Health and Nutrition Centre, Monash Asia Institute, Monash University, Clayton, Victoria, Australia
Widjaja Lukito
Affiliation:
The Asia Pacific Health and Nutrition Centre, Monash Asia Institute, Monash University, Clayton, Victoria, Australia
Valerie Burke
Affiliation:
University of Western Australia School of Medicine and Pharmacology and the Western Australian Institute for Medical Research at Royal Perth Hospital, Perth, Western Australia, Australia
Natalie C. Ward
Affiliation:
University of Western Australia School of Medicine and Pharmacology and the Western Australian Institute for Medical Research at Royal Perth Hospital, Perth, Western Australia, Australia
Richard L. Prince
Affiliation:
University of Western Australia School of Medicine and Pharmacology and the Western Australian Institute for Medical Research at QEII Medical Centre, Perth, Western Australia, Australia
Kevin D. Croft
Affiliation:
University of Western Australia School of Medicine and Pharmacology and the Western Australian Institute for Medical Research at Royal Perth Hospital, Perth, Western Australia, Australia
*
*Corresponding author: Dr Jonathan M. Hodgson, fax +61 8 9224 0246, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Tea and coffee are rich in polyphenols with a variety of biological activities. Many of the demonstrated activities are consistent with favourable effects on the risk of chronic diseases. 4-O-methylgallic acid (4OMGA) and isoferulic acid are potential biomarkers of exposure to polyphenols derived from tea and coffee respectively. 4OMGA is derived from gallic acid in tea, and isoferulic acid is derived from chlorogenic acid in coffee. Our major objective was to explore the relationships of tea and coffee intake with 24 h urinary excretion of 4OMGA and isoferulic acid in human subjects. The relationships of long-term usual (111 participants) and contemporaneously recorded current (344 participants) tea and coffee intake with 24 h urinary excretion of 4OMGA and isoferulic acid were assessed in two populations. 4OMGA was related to usual (r 0·50, P<0·001) and current (r 0·57, P<0·001) tea intake, and isoferulic acid was related to usual (r 0·26, P=0·008) and current (r 0·18, P<0·001) coffee intake. Overall, our present results are consistent with the proposal that 4OMGA is a good biomarker for black tea-derived polyphenol exposure, but isoferulic acid may be of limited usefulness as a biomarker for coffee-derived polyphenol exposure.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2004

References

Bruce, DG, Devine, A & Prince, RL (2002) Recreational physical activity levels in healthy older women: the importance of fear of falling. J Am Geriatr Soc 50, 8489.CrossRefGoogle ScholarPubMed
Caccetta, RAA, Burke, V, Mori, TA et al. (2001) Red wine polyphenols, in the absence of alcohol, reduce lipid peroxidative stress in smoking subjects. Free Radic Biol Med 30, 636642.CrossRefGoogle Scholar
Chesson, A, Provan, GJ, Russell, WR et al. (1999) Hydroxycinnamic acids in the digestive tract of livestock and humans. J Sci Food Agric 79, 373378.3.0.CO;2-6>CrossRefGoogle Scholar
Clifford, MN (1999) Chlorogenic acids and other cinnamates – nature, occurrence and dietary burden. J Sci Food Agric 79, 362372.3.0.CO;2-D>CrossRefGoogle Scholar
Dalais, FS, Rice, GE, Wahlqvist, ML, Hsu-Hage, BHH & Wattanapenpaiboon, N (1998) Urinary excretion of isoflavonoid phytoestrogens in Chinese and Anglo-Celtic populations in Australia. Nutr Res 18, 17031709.CrossRefGoogle Scholar
Dick, IM, Devine, A & Marangou, A (2002) Apolipoprotein E4 is associated with reduced calcaneal quantitative ultrasound measurements and bone mineral density in elderly women. Bone 31, 497502.CrossRefGoogle ScholarPubMed
Harbowy, ME & Ballentine, DA (1997) Tea chemistry. Crit Rev Plant Sci 16, 415480.CrossRefGoogle Scholar
Herrmann, K (1989) Occurrence and content of hydroxycinnamic and hydroxybenzoic acid compounds in foods. Crit Rev Food Sci Nutr 28, 315347.CrossRefGoogle ScholarPubMed
Hertog, ML, Kromhout, D, Aravanis, C et al. (1995) Flavonoid intake and long-term risk of coronary heart disease and cancer in the Seven Countries Study. Arch Int Med 155, 381386.CrossRefGoogle ScholarPubMed
Hodgson, JM, Burke, V, Beilin, LJ, Croft, KD & Puddey, IB (2003) Can black tea influence plasma total homocysteine concentrations? Am J Clin Nutr 77, 907911.CrossRefGoogle ScholarPubMed
Hodgson, JM, Croft, KD, Mori, TA et al. (2002 a) Regular ingestion of tea does not inhibit in vivo lipid peroxidation in humans. J Nutr 132, 5558.CrossRefGoogle Scholar
Hodgson, JM, Morton, LW, Puddey, IB, Beilin, LJ & Croft, KD (2000 a) Gallic acid metabolites are markers of black tea intake in humans. J Agric Food Chem 48, 22762280.CrossRefGoogle ScholarPubMed
Hodgson, JM, Puddey, IB, Burke, V, Watts, GF & Beilin, LJ (2002 b) Regular ingestion of black tea improves brachial artery vasodilator function. Clin Sci 102, 195201.CrossRefGoogle ScholarPubMed
Hodgson, JM, Puddey, IB, Croft, KD et al. (2000 b) Acute effects of ingestion of black and green tea on lipoprotein oxidation. Am J Clin Nutr 71, 11031107.CrossRefGoogle ScholarPubMed
Hodgson, JM, Puddey, IB, Mori, TA et al. (2001) Effects of regular ingestion of black tea on haemostasis and cell adhesion molecules in humans. Eur J Clin Nutr 55, 881886.CrossRefGoogle ScholarPubMed
Kivits, GAA, Vandersman, FJP & Tijburg, LBM (1997) Analysis of catechins from green and black tea in humans: a specific and sensitive colorimetric assay of total catechins in biological fluids. Int J Food Sci Nutr 48, 387392.CrossRefGoogle Scholar
Knekt, P, Kumpulainen, J, Jarvinen, R et al. (2002) Flavonoid intake and risk of chronic diseases. Am J Clin Nutr 76, 560568.CrossRefGoogle ScholarPubMed
Kouris-Blazos, A, Gnardellis, C, Wahlqvist, ML et al. (1999) Are the advantages of the Mediterranean diet transferable to other populations? A cohort study in Melbourne, Australia. Br J Nutr 82, 5761.CrossRefGoogle ScholarPubMed
Kouris-Blazos, A, Wahlqvist, ML, Trichopoulou, A, Polychronopoulos, E & Trichopoulos, D (1996) Health and nutritional status of elderly Greek migrants to Melbourne, Australia. Age Ageing 25, 177189.CrossRefGoogle ScholarPubMed
Meng, XF, Sang, SM, Zhu, NQ et al. (2002) Identification and characterization of methylated and ring-fission metabolites of tea catechins formed in humans, mice, and rats. Chem Res Toxicol 15, 10421050.CrossRefGoogle ScholarPubMed
Morton, LW, Abu-Amsha, CR, Puddey, IB & Croft, KD (2000) Chemistry and biological effects of dietary phenolic compounds: relevance to cardiovascular disease. Clin Exp Pharmacol Physiol 27, 152159.CrossRefGoogle ScholarPubMed
Nardini, M, Cirillo, E, Natella, F & Scaccini, C (2002) Absorption of phenolic acids after coffee consumption. J Agric Food Chem 50, 57355741.CrossRefGoogle ScholarPubMed
Plumb, GW, Garcia-Conesa, MT, Kroon, PA et al. (1999) Metabolism of chlorogenic acid by human plasma, liver, intestine and gut microflora. J Sci Food Agric 79, 390392.3.0.CO;2-0>CrossRefGoogle Scholar
Rechner, AR, Spencer, JP, Kuhnle, G, Hahn, U & Rice-Evans, CA (2001) Novel biomarkers of the metabolism of caffeic acid derivatives in vivo. Free Radic Biol Med 30, 12131222.CrossRefGoogle Scholar
Scalbert, A & Williamson, G (2000) Dietary intake and bioavailability of polyphenols. J Nutr 130, 2073S2085S.CrossRefGoogle ScholarPubMed
Shahrzad, S, Aoyagi, K, Winter, A, Koyama, A & Bitsch, I (2001) Pharmacokinetics of gallic acid and its relative bioavailability from tea in healthy humans. J Nutr 131, 12071210.CrossRefGoogle ScholarPubMed
Shahrzad, S & Bitsch, I (1998) Determination of gallic acid and its metabolites in human plasma and urine by high-performance liquid chromatography. J Chromatogr B 705, 8795.CrossRefGoogle ScholarPubMed
Youdim, KA, Martin, A & Joseph, JA (2000) Incorporation of the elderberry anthocyanins by endothelial cells increases protection against oxidative stress. Free Radic Biol Med 29, 5160.CrossRefGoogle ScholarPubMed