痛风患者淋巴细胞重新合成嘌呤。

P Kamoun, J Chanard, M Brami, J L Funck-Brentano
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引用次数: 2

摘要

1. 提出了一种体外测定人体循环淋巴细胞嘌呤生物合成的方法。嘌呤生物从头合成的早期反应速率是通过将[14C]甲酸掺入n -甲酰基甘氨酰胺核糖核苷酸来确定的,而随后的代谢途径的反应被抗生素氮扎塞林完全抑制。2. 在接受或不接受别嘌呤醇治疗的健康对照者和原发性痛风或继发于肾功能衰竭的高尿酸血症患者中,淋巴细胞合成14c标记的n -甲酰基甘氨酸酰胺核糖核苷酸。3.未经治疗的痛风患者的平均合成高于对照组,但所获得的值与正常范围重叠。继发性高尿酸血症患者的合成值与对照组相同。4. 这些结果与其他通过测量[14C]甘氨酸并入尿尿酸的人所看到的痛风患者从头开始的嘌呤生物合成的不恒定加速一致。
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Purine biosynthesis de novo by lymphocytes in gout.

1. A method of measurement in vitro of purine biosynthesis de novo in human circulating blood lymphocytes is proposed. The rate of early reactions of purine biosynthesis de novo was determined by the incorporation of [14C]formate into N-formyl glycinamide ribonucleotide when the subsequent reactions of the metabolic pathway were completely inhibited by the antibiotic azaserine. 2. Synthesis of 14C-labelled N-formyl glycinamide ribonucleotide by lymphocytes was measured in healthy control subjects and patients with primary gout or hyperuricaemia secondary to renal failure, with or without allopurinol therapy. 3. The average synthesis was higher in gouty patients without therapy than in control subjects, but the values obtained overlap the normal range. In secondary hyperuricaemia the synthesis was at same value as in control subjects. 4. These results are in agreement with the inconstant acceleration of purine biosynthesis de novo in gouty patients as seen by others with measurement of [14C]glycine incorporation into urinary uric acid.

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