Effect of Vitamins C and E on Endogenous Synthesis of N-nitrosamino Acids in Humans: Precursor-product Studies with [15N]nitrate
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The endogenous formation of nitrosoproline (NPRO) following administration of nitrate and proline is reported in ten healthy young adults. There was a relatively constant basal excretion of NPRO, 26 +/- 10 (SD) nmol/day, in excess of amounts found in the diet. This basal synthesis of NPRO was not reduced by ascorbic acid (2 g/day) or alpha-tocopherol (400 mg/day). A significant rise in the excretion of NPRO was observed following the administration of nitrate and proline, ranging from 29 to 318 nmol/24 h with a mean of 100 nmol/24 h. [15N]Nitrate was used as a tracer to study the observed excess excretion of NPRO in urine. The data revealed that urinary NPRO excretion as a result of endogenous synthesis is not totally derived from ingested nitrate as its precursor. The ingestion of ascorbic acid and alpha-tocopherol inhibited the incorporation of [15N]nitrate into NPRO by 81 and 59%, respectively. An additional nitrosamino acid, N-nitrosothiazolidine-4-carboxylic acid, was present in the urine. It was found that N-nitrosothiazolidine-4-carboxylic acid increased 6-fold upon ingestion of nitrate. Ascorbic acid and alpha-tocopherol blocked this nitrate induced synthesis.
Inducible Nitric Oxide Synthase in the Carcinogenesis of Gastrointestinal Cancers.
de Oliveira G, Cheng R, Ridnour L, Basudhar D, Somasundaram V, McVicar D Antioxid Redox Signal. 2016; 26(18):1059-1077.
PMID: 27494631 PMC: 5488308. DOI: 10.1089/ars.2016.6850.
Urinary markers for exposures to alkylating or nitrosating agents.
Wishnok J, Tannenbaum S, Stillwell W, Glogowski J, Leaf C Environ Health Perspect. 1993; 99:155-9.
PMID: 8319614 PMC: 1567041. DOI: 10.1289/ehp.9399155.
Bednar C, Kies C Plant Foods Hum Nutr. 1994; 45(1):71-80.
PMID: 8146105 DOI: 10.1007/BF01091231.
Gerster H Z Ernahrungswiss. 1987; 26(2):125-37.
PMID: 3307183 DOI: 10.1007/BF02019608.
Houghton P, Leach S, Owen R, Mortensen N, Hill M, Williamson R Br J Cancer. 1989; 60(2):231-4.
PMID: 2765371 PMC: 2247036. DOI: 10.1038/bjc.1989.258.