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(13)C-Enrichment of Urinary Uric Acid after l-[Ring-2-(13)C]Histidine Dose in Adult Humans

We determined whether ring-2 carbon of histidine is folate-dependently transferred to carbons 8 (C(8)) and/or 2 (C(2)) in urinary uric acid in humans. Two adults collected each urine void for four days. Aliquots of urine for the first day were used for baseline values; then the subjects ingested 0.7...

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Detalles Bibliográficos
Autores principales: Tamura, Tsunenobu, Baggott, Joseph E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303862/
https://www.ncbi.nlm.nih.gov/pubmed/25608940
http://dx.doi.org/10.3390/nu7010697
Descripción
Sumario:We determined whether ring-2 carbon of histidine is folate-dependently transferred to carbons 8 (C(8)) and/or 2 (C(2)) in urinary uric acid in humans. Two adults collected each urine void for four days. Aliquots of urine for the first day were used for baseline values; then the subjects ingested 0.7 g (3.3 mmol) of l-[ring-2-(13)C]histidine and collected urine for three experimental days. Aliquots were analyzed for percentage (13)C-content at C(2) and C(8) by a liquid-chromatography-mass spectrometry method. Percentage enrichment was determined by subtracting time-of-day paired baseline percentage (13)C-content from experimental percentage (13)C-content for each void. C(2) was predominantly (13)C-enriched in the majority of voids. The percentage enrichments at C(2) for two subjects were 0.14 (±0.028 [SEM], n = 26) and 0.18 (±0.049, n = 21), whereas at C(8), they were 0.008 (±0.006) and −0.005 (±0.008), respectively. The mean C(2)-enrichments were significantly greater than zero (p < 0.01), whereas those of C(8) were not (p > 0.2). The enrichment had a diurnal rhythm peaking in the morning. Our results may be useful in the estimation of the timing for the administration of drugs that interfere with purine nucleotide biosynthesis in the treatment of cancer and autoimmune disease.