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para-Acetamidobenzoylglutamate Is a Suitable Indicator of Folate Catabolism in Rats1

Francis L. Geoghegan, Joseph M. McPartlin, Donald G. Weir and John M. Scott*,2

Departments of Clinical Medicine * Biochemistry, University of Dublin, Trinity College, Dublin, Ireland

The amount of biologically active folate excreted in the urine corresponds to a small fraction of the recommended dietary allowance, suggesting that a large amount of folate is excreted as its catabolites. A strategy of assessing folate requirement by measuring the daily urinary levels of products of folate catabolism depends on the demonstration of an exclusive mechanism of breakdown as well as a suitable marker of the catabolic process. Rats were given [3H] and [14C]folic acid by gastric intubation daily for 10 d to simulate normal dietary intake of the vitamin. Total urine was collected throughout this period as well as for the following 10 d. Reverse-phase HPLC of the radiolabeled urinary products revealed the presence of a variety of intact folates as well as products of C9-N10 scission of the folate molecule, pteridines, para-aminobenzoylglutamate and para-acetamidobenzoylglutmate. We detected no other N10-containing catabolites, nor did we find the oxidized folate derivative ‘4{alpha}-hydroxy-5-methyltetrahydrofolate’. Of all the urinary folate metabolites, only para-acetamidobenzoylglutmate persisted at high levels up to 10 d after radiolabel treatment was withdrawn. We conclude that folate catabolism occurs exclusively through C9-N10 cleavage and that measurement of urinary para-acetamidobenzoylglutmate provides a suitable indicator of daily folate turnover.


KEY WORDS: • rats • folate catabolism • folate requirement • recommended dietary allowance • para-acetamidobenzoylglutamate

1 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.

2 To whom correspondence should be addressed.

Manuscript received 12 September 1994. Revision accepted 25 April 1995.







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