Folic acid treatment decreases plasma total homocysteine concentrations in healthy subjects, but the effects on homocysteine metabolism are unknown. In the present study, we investigated the effect of 3 weeks of oral treatment with 5 mg of folic acid on one-carbon flux rates in 12 healthy subjects, using in vivo stable isotope methods. In addition, we determined the effect of folic acid on blood concentrations of amino acids which may have regulatory roles in homocysteine metabolism, i.e. homocysteine, AdoMet (S-adenosylmethionine), AdoHcy (S-adenosylhomocysteine), serine and glycine. Primed, continuous infusions with [2H3-methyl-1-13C]methionine were used to determine flux rates of methionine transmethylation, homocysteine remethylation and homocysteine trans-sulphuration. Metabolic homocysteine clearance was defined as the ratio of trans-sulphuration and plasma homocysteine level. Folic acid treatment increased the homocysteine remethylation rate by 59% [95% CI (confidence interval), 13–97%; P=0.02] and methionine transmethylation rate by 20% (95% CI, 3–41%; P=0.03). Plasma total homocysteine concentration (−18%; 95% CI, −28 to −9%; P<0.01) and the serine/glycine ratio (−20%; 95% CI, −63 to −6%; P<0.01) decreased significantly, and the AdoMet/AdoHcy ratio (11%; 95% CI, 1–20%; P=0.02) increased significantly. Changes in one-carbon flux rates did not correlate significantly with changes in plasma concentration of these amino acids. In conclusion, folic acid treatment lowered plasma homocysteine concentration and increased whole-body remethylation and transmethylation flux in healthy subjects.
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May 2005
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Research Article|
April 22 2005
Folic acid treatment increases homocysteine remethylation and methionine transmethylation in healthy subjects
Frank STAM;
*Department of Internal Medicine, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
†Institute for Cardiovascular Research, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
Correspondence: Dr Frank Stam, Department of Internal Medicine, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands (email [email protected]).
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Yvo M. SMULDERS;
Yvo M. SMULDERS
*Department of Internal Medicine, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
†Institute for Cardiovascular Research, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
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Coen van GULDENER;
Coen van GULDENER
*Department of Internal Medicine, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
†Institute for Cardiovascular Research, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
§Department of Internal Medicine, Amphia Hospital, Langendijk, PO Box 90517, 4800 RL Breda, The Netherlands
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Cornelis JAKOBS;
Cornelis JAKOBS
‡Department of Clinical Chemistry, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
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Coen D. A. STEHOUWER;
Coen D. A. STEHOUWER
*Department of Internal Medicine, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
†Institute for Cardiovascular Research, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
∥Department of Internal Medicine, Academic Hospital Maastricht, P. Debyelaan 25, 6229 HX Maastricht, The Netherlands
¶Cardiovascular Research Institute Maastricht, Maastricht University, PO Box 5800, 6202 AZ Maastricht, The Netherlands
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Kees de MEER
Kees de MEER
†Institute for Cardiovascular Research, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
‡Department of Clinical Chemistry, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands
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Publisher: Portland Press Ltd
Received:
October 12 2004
Revision Received:
December 21 2004
Accepted:
January 12 2005
Accepted Manuscript online:
January 12 2005
Online ISSN: 1470-8736
Print ISSN: 0143-5221
The Biochemical Society
2005
Clin Sci (Lond) (2005) 108 (5): 449–456.
Article history
Received:
October 12 2004
Revision Received:
December 21 2004
Accepted:
January 12 2005
Accepted Manuscript online:
January 12 2005
Citation
Frank STAM, Yvo M. SMULDERS, Coen van GULDENER, Cornelis JAKOBS, Coen D. A. STEHOUWER, Kees de MEER; Folic acid treatment increases homocysteine remethylation and methionine transmethylation in healthy subjects. Clin Sci (Lond) 1 May 2005; 108 (5): 449–456. doi: https://doi.org/10.1042/CS20040295
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