Metabolomic studies in the inborn error of metabolism alkaptonuria reveal new biotransformations in tyrosine metabolism



Norman, Brendan P ORCID: 0000-0001-9293-4852, Davison, Andrew S ORCID: 0000-0001-5501-4475, Hughes, Juliette H ORCID: 0000-0001-6155-4136, Sutherland, Hazel, Wilson, Peter JM, Berry, Neil G ORCID: 0000-0003-1928-0738, Hughes, Andrew T, Milan, Anna M, Jarvis, Jonathan C, Roberts, Norman B
et al (show 3 more authors) (2022) Metabolomic studies in the inborn error of metabolism alkaptonuria reveal new biotransformations in tyrosine metabolism. GENES & DISEASES, 9 (4). pp. 1129-1142.

Access the full-text of this item by clicking on the Open Access link.

Abstract

Alkaptonuria (AKU) is an inherited disorder of tyrosine metabolism caused by lack of active enzyme homogentisate 1,2-dioxygenase (HGD). The primary consequence of HGD deficiency is increased circulating homogentisic acid (HGA), the main agent in the pathology of AKU disease. Here we report the first metabolomic analysis of AKU homozygous <i>Hgd</i> knockout (<i>Hgd</i> <sup>-/-</sup>) mice to model the wider metabolic effects of <i>Hgd</i> deletion and the implication for AKU in humans. Untargeted metabolic profiling was performed on urine from <i>Hgd</i> <sup>-/-</sup> AKU (<i>n</i> = 15) and <i>Hgd</i> <sup>+/-</sup> non-AKU control (<i>n</i> = 14) mice by liquid chromatography high-resolution time-of-flight mass spectrometry (Experiment 1). The metabolites showing alteration in <i>Hgd</i> <sup>-/-</sup> were further investigated in AKU mice (<i>n</i> = 18) and patients from the UK National AKU Centre (<i>n</i> = 25) at baseline and after treatment with the HGA-lowering agent nitisinone (Experiment 2). A metabolic flux experiment was carried out after administration of <sup>13</sup>C-labelled HGA to <i>Hgd</i> <sup>-/-</sup>(<i>n</i> = 4) and <i>Hgd</i> <sup>+/-</sup>(<i>n</i> = 4) mice (Experiment 3) to confirm direct association with HGA. <i>Hgd</i> <sup>-/-</sup> mice showed the expected increase in HGA, together with unexpected alterations in tyrosine, purine and TCA-cycle pathways. Metabolites with the greatest abundance increases in <i>Hgd</i> <sup>-/-</sup> were HGA and previously unreported sulfate and glucuronide HGA conjugates, these were decreased in mice and patients on nitisinone and shown to be products from HGA by the <sup>13</sup>C-labelled HGA tracer. Our findings reveal that increased HGA in AKU undergoes further metabolism by mainly phase II biotransformations. The data advance our understanding of overall tyrosine metabolism, demonstrating how specific metabolic conditions can elucidate hitherto undiscovered pathways in biochemistry and metabolism.

Item Type: Article
Uncontrolled Keywords: Alkaptonuria, Biotransformation, Metabolism, Metabolomics, Mice
Divisions: Faculty of Health and Life Sciences
Faculty of Health and Life Sciences > Clinical Directorate
Faculty of Health and Life Sciences > Institute of Life Courses and Medical Sciences
Depositing User: Symplectic Admin
Date Deposited: 30 Jun 2021 14:26
Last Modified: 18 Jan 2023 21:37
DOI: 10.1016/j.gendis.2021.02.007
Open Access URL: https://www.sciencedirect.com/science/article/pii/...
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3128295