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Uric acid synthesis by rat liver supernatants from purine bases, nucleosides and nucleotides. Effect of allopurinol
Author(s) -
Bleisch Siegfried,
Sillero Maria A. Günther,
Torrecilla Amparo,
Sillero Antonio
Publication year - 1994
Publication title -
cell biochemistry and function
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.933
H-Index - 61
eISSN - 1099-0844
pISSN - 0263-6484
DOI - 10.1002/cbf.290120403
Subject(s) - uric acid , nucleotide , purine , allopurinol , biochemistry , chemistry , purine metabolism , enzyme , medicine , gene
Abstract The synthesis of uric acid from purine bases, nucleosides and nucleotides has been measured in reaction mixtures containing rat liver supernatant and each one of the following compounds at 1 m M concentration (except xanthine, 0·5 m M and guanosine and guanine, 0·1 mM). The rates of the reaction, expressed as nanomoles of uric acid synthesized g −1 of wet liver min −1 were: ATP, 10; ADP, 37; AMP, 62; adenosine, 108; adenine 6; adenylo‐succinate, 9; IMP 32; inosine, 112; hypoxanthine, 50; GTP, 19; GDP, 19; GMP, 27; guanosine, 34; guanine, 72; XMP, 10; xanthosine, 24; xanthine, 144. These figures divided by 55 correspond to nanomoles of uric acid synthesized min −1 per mg −1 of protein. The rate of synthesis of uric acid obtained with each one of those compounds at 0·1 and 0·05 m M concentrations was also determined. ATP (1 nM) strongly inhibited uric acid synthesis from 0·05 m M AMP (91 per cent) and from 0·05 m M ADP (88 per cent), but not from adenosine. CTP or UTP (1 m M ) also inhibited (by more than 90 per cent) the synthesis of uric acid from 0·05 m M AMP. Xanthine oxidase was inhibited by concentrations of hypoxanthine higher than 0·012 mM. The results favour the view that the level of uric acid in plasma may be an index of the energetic state of the organism. Allopurinol, besides inhibiting uric acid synthesis, reduced the rate of degradation of AMP. The ability of crude extracts to catabolize purine nucleotides to uric acid is an important factor to be considered when some enzymes related to purine nucleotide metabolism, particularly CTP synthase, are measured in crude liver extracts.