QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text (PDF) Purchase Article View Shopping Cart Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Jacob, R. A. Articles by Swendseid, M. E. Search for Related Content PubMed PubMed Citation Articles by Jacob, R. A. Articles by Swendseid, M. E.

In Vivo Methylation Capacity Is Not Impaired in Healthy Men during Short-Term Dietary Folate and Methyl Group Restriction^1,2,3,

Western Human Nutrition Research Center, U.S. Department of Agriculture, Agricultural Research Service, Presidio of San Francisco, CA 94129 ^* School of Public Health, University of California, Los Angeles, CA 90024

Ten healthy adult men were fed a diet low in folate and exogenous methyl groups to study the effects on in vivo methylation capability. The men were housed in a metabolic unit for the entire 108 d of the study. After a 9-d baseline period (Period 1), the men were fed a soy-product-amino acid defined diet for 45 d, which provided 25 µg/d of folate for 30 d (Period 2) and, with a folate supplement, 99 µg/d for 15 d (Period 3). During Period 2 and Period 3, the low methionine and choline diet was supplemented with methionine for half the subjects to vary the dietary methyl group intake. The periods were then repeated over the next 54 d (Periods 4–6), with a crossover of methionine intakes in Period 5 and Period 6. A 1-g oral dose of nicotinamide was given at the end of each period and methylated urine metabolites determined. Other measures related to in vivo methylation capability included urine creatinine, and plasma and urine carnitine. Even with moderate folate depletion, none of these measures was decreased by low methionine and choline intakes. Plasma methionine concentrations were unchanged throughout. Limiting exogenous methyl group intake by restricting dietary methionine and choline did not impair in vivo methylation capabilities for the variables tested, even at low folate intake.

KEY WORDS: • methylation • methyl group • methionine • humans

¹ Project at UCLA supported in part by NIHCA42710 and Westreco, Inc., Van Nuys, CA.

² Reference to a company or product name does not imply approval or recommendation of the product by the U.S. Department of Agriculture to the exclusion of others that may be suitable.

³ The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 USC section 1734 solely to indicate this fact.

⁴ To whom correspondence should be addressed.

Manuscript received 16 August 1994. Revision accepted 1 December 1994.

This article has been cited by other articles:

				S. J Lewis, D. A Lawlor, B. G Nordestgaard, A. Tybjaerg-Hansen, S. Ebrahim, J. Zacho, A. Ness, S. Leary, and G. D. Smith The methylenetetrahydrofolate reductase C677T genotype and the risk of obesity in three large population-based cohorts. Eur. J. Endocrinol., July 1, 2008; 159(1): 35 - 40. [Abstract] [Full Text] [PDF]

				L. M Fischer, K. A. daCosta, L. Kwock, P. W Stewart, T.-S. Lu, S. P Stabler, R. H Allen, and S. H Zeisel Sex and menopausal status influence human dietary requirements for the nutrient choline Am. J. Clinical Nutrition, May 1, 2007; 85(5): 1275 - 1285. [Abstract] [Full Text] [PDF]