Kojima T, Nishina T, Kitamura M, Yamanak H, Nishioka K
Department of Clinical Chemistry, Toranomon Hospital, Tokyo, Japan.
Biomed Chromatogr. 1991 Mar;5(2):57-61. doi: 10.1002/bmc.1130050203.
A new method for the determination of adenine phosphoribosyltransferase (APRT) activity in human erythrocytes is described. APRT activity was assayed by a non-radiochemical method in which adenosine monophosphate (AMP) and AMP metabolites produced from a substrate adenine were converted to inosine by alkaline phosphatase and adenosine deaminase. The inosine thus produced was quantitated by reversed phase HPLC. This method was simple, precise, sensitive and free from interference with other co-existing erythrocyte enzymes. Four patients with 2,8-dihydroxyadenine urolithiasis and others with several disorders in purine metabolism have been studied, showing that the present method is clinically useful for the diagnosis and the evaluation of the severity of some human diseases.
描述了一种测定人红细胞中腺嘌呤磷酸核糖转移酶(APRT)活性的新方法。通过非放射化学方法测定APRT活性,其中底物腺嘌呤产生的一磷酸腺苷(AMP)和AMP代谢产物通过碱性磷酸酶和腺苷脱氨酶转化为肌苷。如此产生的肌苷通过反相高效液相色谱法进行定量。该方法简单、精确、灵敏,且不受其他共存红细胞酶的干扰。对4例2,8 - 二羟基腺嘌呤尿石症患者和其他嘌呤代谢存在多种紊乱的患者进行了研究,表明该方法在临床上可用于某些人类疾病的诊断和严重程度评估。