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II型瓜氨酸血症中精氨琥珀酸尿排泄增加。

Increased urinary excretion of argininosuccinate in type II citrullinemia.

作者信息

Saheki T, Kobayashi K, Inoue I, Matuo S, Hagihara S, Noda T

机构信息

Department of Biochemistry, Faculty of Medicine, Kagoshima University, Japan.

出版信息

Clin Chim Acta. 1987 Dec;170(2-3):297-304. doi: 10.1016/0009-8981(87)90140-9.

Abstract

Although argininosuccinate is a product of the catalytic action of deficient argininosuccinate synthetase in citrullinemia, its concentration was found to be elevated in the urine of patients with type II citrullinemia. Urinary argininosuccinate was identified by two methods; its conversions to anhydride by boiling in an acidic solution and to arginine by the enzymatic action of argininosuccinate lyase. Oral administration of citrulline to patients with type II citrullinemia and control subjects increased urinary argininosuccinate levels. These phenomena are consistent with our previous findings on type II citrullinemia (Adv Exp Med Biol 1983;153:63-76,J Clin Biochem Nutr 1986;1:129-142), namely that renal argininosuccinate synthetase which plays a role in arginine synthesis is not deficient in patients with type II citrullinemia; and that serum arginine levels in patients with type II citrullinemia are rather higher than the controls, and increase after the oral administration of citrulline. The organ-specific deficiency of argininosuccinate synthetase in type II citrullinemia is further confirmed by this paper.

摘要

尽管精氨琥珀酸是瓜氨酸血症中精氨琥珀酸合成酶缺乏催化作用的产物,但在II型瓜氨酸血症患者的尿液中发现其浓度升高。通过两种方法鉴定尿中的精氨琥珀酸;在酸性溶液中煮沸将其转化为酸酐,以及通过精氨琥珀酸裂解酶的酶促作用将其转化为精氨酸。对II型瓜氨酸血症患者和对照受试者口服瓜氨酸会增加尿中精氨琥珀酸水平。这些现象与我们之前关于II型瓜氨酸血症的研究结果一致(《实验生物学与医学进展》1983年;153:63 - 76,《临床生物化学与营养杂志》1986年;1:129 - 142),即参与精氨酸合成的肾精氨琥珀酸合成酶在II型瓜氨酸血症患者中并不缺乏;并且II型瓜氨酸血症患者的血清精氨酸水平高于对照组,口服瓜氨酸后会升高。本文进一步证实了II型瓜氨酸血症中精氨琥珀酸合成酶的器官特异性缺乏。

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