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改良红细胞尿卟啉原I合酶测定及其临床解读。

Modified erythrocyte uroporphyrinogen I synthase assay, and its clinical interpretation.

作者信息

Piepkorn M W, Hamernyik P, Labbé R F

出版信息

Clin Chem. 1978 Oct;24(10):1751-4.

PMID:699283
Abstract

Assay of erythrocyte uroporphyrinogen I synthase is an accepted diagnostic test for acute intermittent porphyria, particularly in those individuals who are asymptomatic or in whom the disease is not biochemically manifested by excretion of excess porphyrin precursor. The assay described is based upon a coupled-enzyme procedure in which added delta-aminolevulinic acid and its dehydratase present in erythrocytes are used to generate porphobilinogen as substrate for uroporphyrinogen synthase. Zinc and dithiothreitol are added with preincubation to give maximum activity and reproducibility. These agents also prevent inhibition by lead. Healthy young women had a mean activity of 40 nmol of porphyrin formed per milliliter of erythrocytes per hour, men and activity of 38 nmol/ml/h. Preparation of control specimens is described. This assay gave within-day CVs ranging from 1.9 to 2.8%. Precautions in interpretation of results are discussed.

摘要

红细胞尿卟啉原 I 合酶检测是急性间歇性卟啉症公认的诊断试验,尤其适用于那些无症状或疾病未通过过量卟啉前体排泄而在生化上表现出来的个体。所述检测基于一种偶联酶程序,其中添加的δ-氨基乙酰丙酸及其存在于红细胞中的脱水酶用于生成胆色素原作为尿卟啉原合酶的底物。添加锌和二硫苏糖醇并进行预孵育以获得最大活性和重现性。这些试剂还可防止铅的抑制作用。健康年轻女性每毫升红细胞每小时形成的卟啉平均活性为40 nmol,男性为38 nmol/ml/h。描述了对照标本的制备方法。该检测的日内变异系数范围为1.9%至2.8%。讨论了结果解读中的注意事项。

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