Increased excretion of formiminoglutamic acid (FIGLU) in the urine has been demonstrated in experimental animals and in patients with folic acid deficiency.¹⁻⁶FIGLU is an intermediate metabolite in the degradation of histidine (Figure). In the presence of tetrahydrofolic acid, the formimino group is transferred from FIGLU to the tetrahydrofolic acid which is thus converted to 5-formiminotetrahydrofolic acid.⁷⁻⁹This conversion apparently is facilitated by the enzyme FIGLU transferase, which has been found in hog liver.¹⁰5-Formiminotetrahydrofolic acid is then converted by a series of reactions to 10-formyltetrahydrofolic acid, a labile, highly active compound in formyl transfer reactions.⁹,¹⁰If tetrahydrofolic acid is not present, which is the case in folic-acid-deficient subjects, this transfer of the formimino group cannot take place, and FIGLU is then excreted in the urine. Normally, only a very small amount is demonstrable in the urine. Even in folic-acid-deficient persons the FIGLU excretion may be
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FRANK C. CARTER (1961) studied this question.
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