Literature DB >> 12663290

Can black tea influence plasma total homocysteine concentrations?

Jonathan M Hodgson1, Valerie Burke, Lawrence J Beilin, Kevin D Croft, Ian B Puddey.   

Abstract

BACKGROUND: Polyphenols can act as acceptors of methyl groups during the metabolism of methionine to homocysteine. This may result in elevations in plasma total homocysteine (tHcy) concentrations after ingestion of polyphenol-rich beverages such as tea.
OBJECTIVES: Our major objective was to determine whether regular, moderate-to-high intakes of black tea alter tHcy concentrations. We also assessed the relation between the degree of O-methylation of tea-derived polyphenols and the change in tHcy with regular ingestion of tea.
DESIGN: Twenty-two subjects completed a randomized, controlled crossover study. Subjects consumed 1250 mL black tea/d (5 cups each containing 2 g tea leaves in 250 mL boiled water) and 1250 mL hot water/d for 4 wk each. Fasting tHcy concentrations and 24-h urinary excretion of 4-O-methylgallic acid (4OMGA, the major O-methylated metabolite of gallic acid) were measured at the end of each period. 4OMGA was used as a marker of overall O-methylation of tea-derived polyphenols.
RESULTS: Black tea did not significantly alter mean (+/- SEM) tHcy concentrations (9.9 +/- 0.5 and 10.0 +/- 0.5 micro mol/L for the hot water and black tea periods, respectively). However, the increased excretion of 4OMGA as a consequence of black tea consumption was positively associated with the change in tHcy from the hot water period to the black tea period (r = 0.55, P = 0.008). Subjects in the bottom quartile of increase in 4OMGA excretion had a significant decrease in tHcy (-0.28 +/- 0.10 micro mol/L; P = 0.046), and those in the top quartile had a significant increase in tHcy (0.78 +/- 0.16 micro mol/L; P = 0.005).
CONCLUSIONS: Overall, regular ingestion of black tea did not alter mean tHcy concentrations. However, individual differences in O-methylation of polyphenolic compounds may influence the ultimate effects of black tea on tHcy.

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Year:  2003        PMID: 12663290     DOI: 10.1093/ajcn/77.4.907

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  7 in total

1.  Mechanism-based pharmacokinetic-pharmacodynamic modeling of bidirectional effect of danshensu on plasma homocysteine in rats.

Authors:  Yuancheng Chen; Yanguang Cao; Jia Zhou; Xiaoquan Liu
Journal:  Pharm Res       Date:  2009-05-07       Impact factor: 4.200

2.  A 6-month randomized pilot study of black tea and cardiovascular risk factors.

Authors:  Kenneth J Mukamal; Kristen MacDermott; Joe A Vinson; Noriko Oyama; Warren J Manning; Murray A Mittleman
Journal:  Am Heart J       Date:  2007-10       Impact factor: 4.749

3.  Beneficial effects of danshensu, an active component of Salvia miltiorrhiza, on homocysteine metabolism via the trans-sulphuration pathway in rats.

Authors:  Yg Cao; J G Chai; Y C Chen; J Zhao; J Zhou; J P Shao; C Ma; X D Liu; X Q Liu
Journal:  Br J Pharmacol       Date:  2009-04-30       Impact factor: 8.739

4.  A six-month crossover chemoprevention clinical trial of tea in smokers and non-smokers: methodological issues in a feasibility study.

Authors:  Chiranjeev Dash; Fung-Lung Chung; Joy Ann Phillips Rohan; Emily Greenspan; Patrick D Christopher; Kepher Makambi; Yukihiko Hara; Kenneth Newkirk; Bruce Davidson; Lucile L Adams-Campbell
Journal:  BMC Complement Altern Med       Date:  2012-07-16       Impact factor: 3.659

5.  Effect of black tea consumption on blood cholesterol: a meta-analysis of 15 randomized controlled trials.

Authors:  Dongmei Wang; Canhuang Chen; Yu Wang; Jiaxing Liu; Rongkai Lin
Journal:  PLoS One       Date:  2014-09-19       Impact factor: 3.240

6.  The relationship between regular tea drinking and calcification of the coronary arteries.

Authors:  Amir Reza Sajjadieh Khajouui; Jamshid Najafian; Reza Talebzadeh; Majid Nejati; Mohaddeseh Behjati
Journal:  J Cardiovasc Thorac Res       Date:  2022-06-21

Review 7.  Green and black tea for the primary prevention of cardiovascular disease.

Authors:  Louise Hartley; Nadine Flowers; Jennifer Holmes; Aileen Clarke; Saverio Stranges; Lee Hooper; Karen Rees
Journal:  Cochrane Database Syst Rev       Date:  2013-06-18
  7 in total

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