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[尿酸代谢的遗传性疾病——分类、酶学及DNA诊断]

[Inherited disorders of uric acid metabolism--classification, enzymatic- and DNA-diagnosis].

作者信息

Iwahana H, 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):3303-8.

PMID:8976110
Abstract

Uric acid is the end product of purine metabolism in human. Then, the enzymatic abnormalities, concerning purine metabolism, cause disorders of uric acid metabolism including hyperuricemia and hypouricemia. The superactivity of 5-phosphoribosyl-pyrophosphate (PRPP) synthetase and deficiency of hypoxanthine-guanine phosphoribosyltransferase (HGPRT) caused hyperuricemia. In glycogen storage diseases of type I, III, V, and VII, decreased energy supply induces hyperuricemia by accelerating ATP degradation. Deficiencies of xanthine oxidase (XO), purine nucleoside phosphorylase (PNP), and PRPP were reported causing hypouricemia. Many methods for DNA-diagnosis were developed including Southern blot, Northern blot, PCR-SSCP (polymerase chain reaction-single strand conformation polymorphism), PCR-RFLP (restriction fragment length polymorphism), and allele specific oligonucleotide hybridization etc.

摘要

尿酸是人体嘌呤代谢的终产物。那么,与嘌呤代谢相关的酶异常会导致尿酸代谢紊乱,包括高尿酸血症和低尿酸血症。5-磷酸核糖焦磷酸(PRPP)合成酶活性过高和次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HGPRT)缺乏会导致高尿酸血症。在I型、III型、V型和VII型糖原贮积病中,能量供应减少通过加速ATP降解诱导高尿酸血症。据报道,黄嘌呤氧化酶(XO)、嘌呤核苷磷酸化酶(PNP)和PRPP缺乏会导致低尿酸血症。已经开发出许多DNA诊断方法,包括Southern印迹、Northern印迹、聚合酶链反应-单链构象多态性(PCR-SSCP)、聚合酶链反应-限制性片段长度多态性(PCR-RFLP)以及等位基因特异性寡核苷酸杂交等。

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