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[嘌呤核苷酸的代谢与尿酸的产生]

[Metabolism of purine nucleotides and the production of uric acid].

作者信息

Yamaoka T, Itakura M

机构信息

Otsuka Department of Clinical and Molecular Nutrition, School of Medicine, University of Tokushima.

出版信息

Nihon Rinsho. 1996 Dec;54(12):3188-94.

PMID:8976090
Abstract

The molecular and biochemical aspects of purine nucleotide biosynthesis through de novo and salvage pathways, the production of uric acid, and their regulation mechanisms are reviewed for further understanding of hyperuricemia and gout. The metabolic rate of purine nucleotide biosynthesis is chiefly determined by the regulation of the de novo pathway, especially amidophosphoribosyltransferase and PRPP synthetase, and the accumulation of uric acid results from the acceleration of de novo biosynthesis and catabolism of purine nucleotide or the decrease in urinary excretion of uric acid. Moreover, several enzyme mutations of purine nucleotide metabolism are also clinically important including gout with hyperactive HPRT and the deficiency of HPRT (Lesch-Nyhan syndrome), adenylosuccinate lyase, xanthine oxidase, APRT, PNP, or ADA (SCID) with gene therapy.

摘要

本文综述了嘌呤核苷酸通过从头合成途径和补救途径进行生物合成的分子和生化方面、尿酸的产生及其调节机制,以进一步了解高尿酸血症和痛风。嘌呤核苷酸生物合成的代谢速率主要由从头合成途径的调节决定,尤其是酰胺磷酸核糖转移酶和PRPP合成酶,尿酸的积累是由于嘌呤核苷酸从头生物合成和分解代谢加速或尿酸尿排泄减少所致。此外,嘌呤核苷酸代谢的几种酶突变在临床上也很重要,包括伴有高活性HPRT的痛风和HPRT缺乏症(莱施-奈恩综合征)、腺苷琥珀酸裂解酶、黄嘌呤氧化酶、APRT、PNP或ADA(重症联合免疫缺陷)以及基因治疗。

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