Literature DB >> 2731378

Metabolism of pyrazinamide and allopurinol in hereditary xanthine oxidase deficiency.

T Yamamoto1, K Higashino, N Kono, M Kawachi, M Nanahoshi, S Takahashi, M Suda, T Hada.   

Abstract

The metabolism of pyrazinamide and allopurinol was studied in three xanthinuric patients from two families with hereditary xanthinuria to determine whether both substrates were oxidized only by xanthine oxidase or by other oxidases as well. One xanthinuric patient could neither metabolize pyrazinamide into 5-hydroxypyrazinamide nor allopurinol into oxypurinol. Two xanthinuric patients could metabolize both pyrazinamide into 5-hydroxypyrazinamide and allopurinol into oxypurinol but could not oxidize pyrazinoic acid to 5-hydroxypyrazinoic acid. These findings suggest that xanthinuria comprises at least two subgroups.

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Year:  1989        PMID: 2731378     DOI: 10.1016/0009-8981(89)90348-3

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  2 in total

1.  Xanthine urolithiasis: ultrastructure analysis of renal and bladder calculi.

Authors:  K Kario; T Matsuo; H Tankawa
Journal:  Int Urol Nephrol       Date:  1991       Impact factor: 2.370

Review 2.  Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.

Authors:  Kimiyoshi Ichida; Yoshihiro Amaya; Ken Okamoto; Takeshi Nishino
Journal:  Int J Mol Sci       Date:  2012-11-21       Impact factor: 5.923

  2 in total

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