Journal of Nutrition LabDiet, Your World of Nutritional Answers

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kownacki-Brown, P. A.
Right arrow Articles by Gregory, J. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kownacki-Brown, P. A.
Right arrow Articles by Gregory, J. F., III

Urinary Excretion of Deuterium-Labeled Folate and the Metabolite p-Aminobenzoylglutamate in Humans1,2,3,4,

Patricia A. Kownacki-Brown, Changzheng Wang, Lynn B. Bailey, John P. Toth and Jesse F. Gregory, III5

Food Science and Human Nutrition Department, University of Florida, Gainesville, FL 32611-0370

Stable isotopic methods were employed to determine the proportion of ingested folate excreted as the metabolite p-aminobenzoylglutamate (pABG, free and N-acetyl) in urine. Adult male subjects (n = 7) were maintained on a 4.54 µmol/d (2 mg/d) folate saturation regimen. After 7 d, subjects were given a mixed oral dose containing 0.67 µmol (300 µg) each of bideuterofolic acid (d2) and tetradeutero-folic acid (d4). Urine was collected for the following 48 h and analyzed for folate and pABG. The extent of deuterium labeling of urinary folate and pABG was determined by gas chromatography-mass spectrometry. urinary total pABG excretion increased less than twofold as a result of the folate saturation, whereas urinary folate increased over 10-fold. Urinary d2 and d4 folates each contained 14–15% of the respective oral doses of labeled compounds, whereas urinary d2 and d4 pABG comprised only 0.98–1.15% of the labeled doses. Molar ratios (d2/d4) of excreted folate and pABG indicated that there was no in vivo isotopic discrimination between the labeled folates. Urinary pABG accounted for 5.1 ± 0.6% of total ingested folate, whereas labeled pABG was about 6.7–7.6% of the excretion of labeled compounds (i.e., labeled folate + pABG). This study indicated that pABG is not a major excretory product during folate supplementation, but its relative importance may increase in conditions of reduced folate nutriture.


KEY WORDS: • folate • stable isotope • humans • p-aminobenzoylglutamate

1 Presented in part at the Annual Meeting of the Federation of American Societies for Experimental Biology, April 1992, Anaheim, CA [Gregory, J. F., Brown, P. A., Bailey, L. B. & Toth, J. P. (1992) Urinary excretion of deuterium-labeled folate and the metabolite p-aminobenzoylglutamate in human subjects. FASEB J. 6: A150 (abs.)].

2 Supported by grant # 88-37200-3620 from the U.S. Department of Agriculture, Competitive Research Grants Program.

3 Florida Agricultural Experiment Station Journal Series no. R-02806.

4 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.

5 To whom correspondence should be addressed.

Manuscript received 18 November 1992. Revision accepted 5 February 1993.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Copyright © 1993 by American Society for Nutrition