Absorption of ferulic acid from low-alcohol beer

References

• Renaud S., de Lorgeril M. Wine, alcohol, platelets and the French paradox for coronary heart disease. Lancet 1992; 339: 1523–1526
   PubMed Web of Science ®Google Scholar
• Hertog M.G.L., Feskens E.J.M., Hollman P.C.H., Katan M.B., Kromhout D. Dietary flavonoids, antioxidant vitamins and coronary heart disease. The Zutphen elderly study. The Lancet 1993; 342: 1007–1011
   PubMed Web of Science ®Google Scholar
• Hertog M.G.L., Kromhout D., Aravanis C., Blackburn H., Buzina R., Fidanza F., Giampoli S., Jansen A., Menotti A., Nedeljkovic S. Flavonoid intake and long-term risk of coronary heart disease and cancer in the Seven Countries Study. Archives of Internal Medicine 1995; 155: 381–386
   PubMed Web of Science ®Google Scholar
• Keli S.O., Hertog M.G.L., Feskens E.J.M., Kromhout D. Flavonoids, antioxidant vitamins and risk of stroke. The Zutphen Study. Archives of Internal Medicine 1996; 156: 637–642
   PubMed Web of Science ®Google Scholar
• Knekt P., Jarvinen R., Reunanen A., Maatela J. Flavonoid intake and coronary mortality in Finland: a cohort study. British Medical Journal 1996; 312: 478–481
   PubMed Web of Science ®Google Scholar
• Sesso H.D., Gaziano J.M., Buring J.E., Hennekens C.H. Coffee and tea intake and the risk of myocardial infarction. American Journal of Epidemiology 1999; 149: 162–167
   PubMed Web of Science ®Google Scholar
• Fuhrman B., Lavy A., Aviram M. Consumption of red wine with meals reduces the susceptibility of human plasma and low-density lipoproteins in volunteers. American Journal of Clinical Nutrition 1995; 61: 549–554
   PubMed Web of Science ®Google Scholar
• Nigdikar S.V., Williams N.R., Griffin B.A., Howard A.N. Consumption of red wine polyphenols reduces the susceptibility low-density lipoproteins to oxidation in vivo. American Journal of Clinical Nutrition 1998; 68: 258–265
   PubMed Web of Science ®Google Scholar
• Ishikawa T., Suzukawa M., Ito T., Yoshida H., Ayaori M., Nishikawa M., Yonemura A., Hara Y., Nakamura H. Effect of tea flavonoid supplementation on the susceptibility of low-density lipoprotein to oxidative modification. American Journal of Clinical Nutrition 1997; 66: 261–266
   PubMed Web of Science ®Google Scholar
• Pietta P., Simonetti P., Roggi C., Brusamolino A., Pellegrini N., Maccarini L., Testolin G. Dietary flavonoids and oxidative stress. Special Publication of the Chemical Society 1996; 181: 249–255
   Google Scholar
• Hertog M.G.L., Sweetman P.M., Fehily A.M., Elwood P.C., Kromhout D. Antioxidant flavonols and ischaemic heart disease in a Welsh population of men. The Caerphilly Study. American Journal of Clinical Nutrition 1997; 65: 1489–1494
   PubMed Web of Science ®Google Scholar
• Rimm E.B., Katan M.B., Ascherio A., Stampfer M.J., Willett W.C. Relation between intake of flavonoids and risk for coronary heart disease in male health professionals. Annals of Internal Medicine 1996; 125: 384–389
   PubMed Web of Science ®Google Scholar
• de Rijke Y.B., Demacker P.N.M., Assen N.A., Sloots I.M., Katan M.B., Stalenhoef A.F.H. Red wine consumption does not affect oxidizability of low-density lipoproteins in volunteers. American Journal of Clinical Nutrition 1996; 63: 329–334
   PubMed Web of Science ®Google Scholar
• van het Hof K.H., de Boer H.S.M., Wiseman S.A., Westrate J.A., Tijburg L.B.M. Consumption of green tea does not increase the resistance of LDL to oxidation in humans. American Journal of Clinical Nutrition 1997; 66: 1125–1232
   PubMed Web of Science ®Google Scholar
• Janssen P.L.T.M.K., Mensink R.P., Cox F.J.J., Harryvan J.L., Hovenier R., Hollman P.C.H., Katan M.B. Effects of the flavonoids quercetin and apigenin on haemostasis in healthy volunteers: results from in vitro and a dietary supplement study. American Journal of Clinical Nutrition 1998; 67: 255–262
   PubMed Web of Science ®Google Scholar
• Goldbohm, R.A., et al. Flavonoid intake and risk of cancer: a prospective cohort study. American Journal of Epidemiology 1995; 141: S61–S61
   PubMed Web of Science ®Google Scholar
• Rice-Evans C., Miller N.J., Paganga G. Structure-antioxidant activity relationships of flavonoids and phenolic acids. Free Radical Biology and Medicine 1996; 20: 933–956
   PubMed Web of Science ®Google Scholar
• Pannala A.S., Rice-Evans C., Halliwell B., Singh S. Inhibition of peroxynitrite-mediated tyrosine nitration by catechin polyphenols. Biochemical and Biophysical Research Communications 1997; 232: 164–168
   PubMed Web of Science ®Google Scholar
• Pannala A.S., Razaq R., Halliwell B., Singh S., Rice-Evans C.A. Inhibition of peroxynitrite-dependent tyrosine nitration by hydroxycinnamates: nitration or electron donation?. Free Radical Biology and Medicine 1998; 24: 594–606
   PubMed Web of Science ®Google Scholar
• Kerry N., Rice-Evans C.A. Peroxynitrite oxidises catechols to o-quinones. FEBS Letters 1998; 437: 167–171
   PubMed Web of Science ®Google Scholar
• Kerry N., Rice-Evans C.A. Inhibition of peroxynitrite-mediated oxidation of dopamine by flavonoid and phenolic antioxidants and their structural relationships. Journal of Neurochemistry 1999; 73: 247–253
   PubMed Web of Science ®Google Scholar
• Rice-Evans C.A., Miller N. Antioxidants — the case for fruit and vegetables in the diet. British Food Journal 1995; 97: 35–40
   Google Scholar
• Cao G., Sofic E., Prior R.L. Antioxidant capacity of tea and common vegetables. Journal of Agriculture and Food Chemistry 1996; 44: 3426–3431
   Web of Science ®Google Scholar
• Wang H., Cao G., Prior R.L. Total antioxidant capacity of fruits. Journal of Agriculture and Food Chemistry 1996; 44: 701–705
   Web of Science ®Google Scholar
• Paganga G., Miller N., Rice-Evans C. The polyphenolic content of fruit and vegetables and their antioxidant activities. What does a serving constitute?. Free Radical Research 1999; 30: 153–162
   PubMed Web of Science ®Google Scholar
• Hollman P.C.H., van der Gaag M.S., Mengelers M.J.B., van Trijp J.M.P., de Vries J.H.M., Katan M.B. Absorption and disposition kinetics of the dietary antioxidant quercetin in man. Free Radical Biology and Medicine 1996; 21: 703–707
   PubMed Web of Science ®Google Scholar
• Hollman P.C.H., van Trijp J.M.P., Buysman M.N.C.P., van der Gaag M.S., Mengelers M.J.B., de Vries J.H.M., Katan M.B. Relative bioavailability of the antioxidant flavonoid quercetin from various foods in man. FEBS Letters 1997; 418: 152–156
   PubMed Web of Science ®Google Scholar
• Paganga G., Rice-Evans C.A. The identification of flavonoids as glycosides in plasma. FEBS Letters 1997; 401: 78–82
   PubMed Web of Science ®Google Scholar
• Nielsen S.E., Kall M., Justesen U., Schou A., Dragsted L.O. Human absorption and excretion of flavonoids after broccoli consumption. Cancer Letters 1997; 114: 173–174
   PubMed Web of Science ®Google Scholar
• Pietta P.G., Gardana C., Mauri P.L. Identification of Gingko biloba flavonol metabolites after oral administration in humans. Journal of Chromatography B 1997; 693: 249–255
   PubMed Web of Science ®Google Scholar
• Fuhr U., Kummert A.L. The fate of naringin in humans: a key to grapefruit juice-drug interactions. Clinical Pharmacology and Therapeutics 1995; 58: 365–373
   PubMed Web of Science ®Google Scholar
• Ameer B., Weintraub R.A., Johnson J.V., Yost R.A., Rousseff R.L. Flavanone absorption after naringin, hesperidin and citrus administration. Clinical Pharmacology and Therapeutics 1996; 60: 34–40
   PubMed Web of Science ®Google Scholar
• Das N.P. Studies on flavonoid metabolism. Absorption and metabolism of (+)-catechin in man. Biochemical Pharmacology 1971; 20: 3435–3445
   PubMed Web of Science ®Google Scholar
• Hackett A.M., Griffiths L.A., Wermeille M. The quantitative disposition of 3-O-methyl-[U-14C] in man following oral administration. Xenobiotica 1985; 15: 907–914
   PubMed Web of Science ®Google Scholar
• Lee M-J., Yang Z.-Y., Li H., Chen L., Sun Y., Gobbo S., Balantine D.A., Yang C.S. Analysis of plasma and urinary tea polyphenols in human subjects. Cancer Epidemiology, Biomarkers and Prevention 1995; 4: 33 393–33 399
   Web of Science ®Google Scholar
• Bourne L.C., Rice-Evans C.A. Bioavailability of ferulic acid. Biochemical and Biophysical Research Communications 1998; 253: 222–227
   PubMed Web of Science ®Google Scholar
• de Vries J.H.M., Hollman P.C.H., Meyboom S., Buysman M.N.C.P., Zock P.L., van Staveren W.A., Katan M.B. Plasma concentrations and urinary excretion of the antioxidant flavonols quercetin and kaempferol as biomarkers for dietary intake. American Journal of Clinical Nutrition 1998; 68: 60–65
   PubMed Web of Science ®Google Scholar
• Bourne L.C., Rice-Evans C.A. Urinary detection of hydroxycinnamates and flavonoids in humans after high dietary intake of fruit. Free Radical Research 1998; 28: 429–438
   PubMed Web of Science ®Google Scholar
• Lapidot T., Harel S., Granit R., Kanner J. Bioavailability of red wine anthocyanins as detected in human urine. Journal of Agriculture and Food Chemistry 1998; 46: 4297–4302
   Web of Science ®Google Scholar
• Gramshaw J.W. Phenolic constituents of beer and brewing materials. Journal of the Institute of Brewing 1967; 73: 258–270
   Google Scholar
• McMurrough, Roche G.P., Cleary K.G. Phenolic acid in beers and worts. Journal of the Institute of Brewing 1984; 90: 181–187
   Web of Science ®Google Scholar
• Huang M-T., Ferraro T. Phenolic compounds in foods and cancer prevention. Phenolic Compounds in Food and their Effects on Health II, M.-T. Huang, C.-H. Ho, C.Y. Lee. ACS Symposium series 507, Washington 1992, In Chapter 2
   Google Scholar
• Miranda C.L., Stevens J.F., Helmrich A., Henderson M.C., Rodriguez R.J., Deinzer M.L., Barnes D.W., Buhler D.R. Cytotoxic and antiproliferative effects of prenylated chalcones in human cancer cell lines and in cultural rat hepatocytes. Food Chemistry and Toxicology 1999, in press
   PubMed Web of Science ®Google Scholar
• Henderson M.C., Miranda C.L., Stevens J.F., Deinzer M.L., Buhler D.R. In vitro inhibition of carcinogenic metabolism by flavonoids from hops (Humulus lupulus) in various species. The Toxicologist 1998; 42: 185–185
   Google Scholar
• Madigan D., McMurrough I. Rapid determination of 4-vinyl guaiacol and ferulic acid in beers and worts by high-performance liquid chromatography. Journal of the American Society of Brewing Chemists 1994; 52: 152–155
   Web of Science ®Google Scholar
• Das N.P. Studies on flavonoid metabolism. Absorption and metabolism of (+)-catechin in man. Biochemical Pharmacology 1971; 20: 3435–3445
   PubMed Web of Science ®Google Scholar
• Hackett A.M., Griffiths L.A., Wermeille M. The quantitative disposition of 3-O-methyl-(+)-[U-14C] catechin in man following oral administration. Xenobiotica 1985; 15: 907–914
   PubMed Web of Science ®Google Scholar
• Zupfer J.M., Churchill K.E., Rasmusson D.C., Fulcher R.G. Variation in ferulic acid concentration among diverse barley cultivars measured by HPLC and microspectrophotometry. Journal of Agriculture and Food Chemistry 1998; 46: 1350–1354
   Web of Science ®Google Scholar
• Nordkvist E., Salomonsson A.-C., Aman P. Distribution of insoluble bound phenolic acids in barley grain. Journal of the Science of Food and Agriculture 1993; 35: 657–661
   Google Scholar