Quantification of the flux of tyrosine pathway metabolites during nitisinone treatment of Alkaptonuria

Milan, AM ORCID: 0000-0002-0452-2338, Hughes, AT, Davison, AS ORCID: 0000-0001-5501-4475, Khedr, M ORCID: 0000-0002-4998-2397, Rovensky, J, Psarelli, EE ORCID: 0000-0002-3102-0288, Cox, TF, Rhodes, NP ORCID: 0000-0002-5173-7032, Gallagher, JA and Ranganath, LR (2019) Quantification of the flux of tyrosine pathway metabolites during nitisinone treatment of Alkaptonuria. SCIENTIFIC REPORTS, 9 (1). 10024-.

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Official URL: http://dx.doi.org/10.1038/s41598-019-46033-x

Abstract

Nitisinone decreases homogentisic acid (HGA) in Alkaptonuria (AKU) by inhibiting the tyrosine metabolic pathway in humans. The effect of different daily doses of nitisinone on circulating and 24 h urinary excretion of phenylalanine (PA), tyrosine (TYR), hydroxyphenylpyruvate (HPPA), hydroxyphenyllactate (HPLA) and HGA in patients with AKU was studied over a four week period. Forty AKU patients, randomised into five groups of eight patients, received doses of 1, 2, 4 or 8 mg of nitisinone daily, or no drug (control). Metabolites were analysed by tandem mass spectrometry in 24 h urine and serum samples collected before and after nitisinone. Serum metabolites were corrected for total body water and the sum of 24 hr urine plus total body water metabolites of PA, TYR, HPPA, HPLA and HGA were determined. Body weight and urine urea were used to check on stability of diet and metabolism over the 4 weeks of study. The sum of quantities of urine metabolites (PA, TYR, HPPA, HPLA and HGA) were similar pre- and post-nitisinone. The sum of total body water metabolites were significantly higher post-nitisinone (p < 0.0001) at all doses. Similarly, combined 24 hr urine:total body water ratios for all analytes were significantly higher post-nitisinone, compared with pre-nitisinone baseline for all doses (p = 0.0002 - p < 0.0001). Significantly higher concentrations of metabolites from the tyrosine metabolic pathway were observed in a dose dependant manner following treatment with nitisinone and we speculate that, for the first time, experimental evidence of the metabolite pool that would otherwise be directed towards pigment formation, has been unmasked.

Item Type:	Article
Uncontrolled Keywords:	Humans, Alkaptonuria, Nitrobenzoates, Homogentisic Acid, Cyclohexanones, Phenylalanine, Tyrosine, Adult, Middle Aged, Female, Male, Pigments, Biological, Tandem Mass Spectrometry
Depositing User:	Symplectic Admin
Date Deposited:	12 Jul 2019 14:47
Last Modified:	19 Jan 2023 00:37
DOI:	10.1038/s41598-019-46033-x
Open Access URL:	https://doi.org/10.1038/s41598-019-46033-x
Related URLs:	Author Publisher
URI:	https://livrepository.liverpool.ac.uk/id/eprint/3049667