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Department of Food Science and Human Nutrition, University of Florida, Gainesville, FL 32611
* Department of Medicine, University of Florida, Gainesville, FL 32611
Fisons Pharmaceuticals, Divisional Research and Development, Rochester, NY 14603
Six healthy men (2231 y) were supplemented for 4 wk with folic acid labeled with deuterium [3',5'-2H2; 3.6 µmol/d (1.6 mg/d)] to permit evaluation of in vivo kinetics of this vitamin. Total folate in urine, serum and erythrocytes was determined by microbiological assay, and isotopic labeling of urinary and erythrocyte folate was determined by gas chromatographymass spectrometry. During supplementation, serum folate reached maximal concentration in
18 d, whereas excretion of total and deuterium-labeled folates increased rapidly and reached isotopic steady state in 12 wk. Isotopic labeling of erythrocyte folate increased continually over the entire supplementation period. Upon cessation of supplementation, red blood cell folate and urinary folate excretion (total and labeled) decreased linearly. The decline in total serum folate could be described with a biexponential model that yielded a slow-phase half-life of 18.7 ± 2.3 d. This model also indicated a turnover of 4.5% of the total body folate pool per day. Pool sizes of total body folate before and after supplementation (at steady state) were calculated to be 10 µmol (4.4 mg) and 98.9 µmol (43.7 mg), respectively. These kinetic data and stable isotope methodology may be used to address a wide range of experimental questions related to folate metabolism.
KEY WORDS: folate supplementation deuterium kinetics humans
1 Supported in part by grant 86-CRCR-1-1240 from the U.S. Department of Agriculture Competitive Research Grants Office.
2 Florida Agricultural Experiment Station Journal Series No. R-02037.
3 To whom correspondence and reprint requests should be addressed.
Manuscript received 14 November 1991. Revision accepted 15 January 1992.