Hultberg, Malin
- Department of Crop Science, Swedish University of Agricultural Sciences
Research article2006Peer reviewed
Hultberg M, Isaksson A, Andersson A, Hultberg B
Objective: The metabolism of homocysteine is influenced by several dietary factors, including folate, cobalamin and possibly also the intake of polyhydroxylated phenolic compounds (polyphenols), which were shown to increase plasma homocysteine (tHcy) concentration. In order to reveal the cause of the increased plasma tHcy, we have therefore investigated the effects of a polyphenol in cell cultures from human cell lines. Design and methods: We have studied the influence of the polyphenol quercetin (Quer) on intra- and extracellular homocysteine concentrations in HeLa and hepatoma cell cultures. Results: The main finding is an increased concentration of extracellular homocysteine in the presence of Quer in hepatoma cell cultures, whereas there were no significant changes of homocysteine concentration in HeLa cell cultures. There was no effect on cellular growth, as judged by cell protein. The presence of adenosyl-dialdehyde, an inhibitor of adenosyl-homocysteine hydrolase, abolished the increased extracellular concentration of homocysteine observed in hepatoma cell cultures in the presence of Quer. Conclusion: The antioxidative agent Quer strongly increased the extracellular concentration of homocysteine in hepatoma cell cultures probably due to increased cellular methylation. In the human body, the same phenomenon might lead to increased plasma tHcy. Since elevated plasma tHcy is associated with premature vascular disease, high long-lasting dietary intake of polyphenols might be harmful. The interaction between Quer and homocysteine turnover may therefore warrant a re-evaluation of polyphenols as relatively harmless antioxidative food supplements or therapeutic antioxidative agents. (c) 2005 The Canadian Society of Clinical Chemists. All rights reserved
HeLa cell lines; homocysteine; hepatoma cell lines; methylation; polyphenol; quercetin
Clinical Biochemistry
2006, Volume: 39, number: 2, pages: 160-163 Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Food Science
DOI: https://doi.org/10.1016/j.clinbiochem.2005.11.002
https://res.slu.se/id/publ/14914