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痛风患者淋巴细胞中嘌呤的从头合成

Purine synthesis de novo in lymphocytes from patients with gout.

作者信息

Gordon R B, Counsilman A C, Cross S M, Emmerson B T

出版信息

Clin Sci (Lond). 1982 Nov;63(5):429-35. doi: 10.1042/cs0630429.

Abstract
  1. Variables that affect the measurement of purine synthesis de novo in human lymphocytes were studied and a reliable method of measurement of purine synthetic activity in these cells was established. 2. Purine synthesis de novo was measured as the rate of incorporation of [14C] formate into alpha-N-formylglycinamide ribonucleotide when further steps in the biosynthetic pathway had been blocked by azaserine. Incubation was carried out in a synthetic medium with a high phosphate concentration (25 mmol/l). 3. Purine synthesis de novo was measured in lymphocytes obtained on several occasions both from control subjects and from patients with gout, particularly those who tended to overproduce urate as suggested by high values of urinary urate. 4. Lymphocytes obtained from each individual on different occasions showed considerable variations in purine biosynthetic activity. This variation was such that there was no difference between the mean values obtained for the gouty subjects and the control subjects. 5. No correlation was obtained between the mean purine synthetic activity de novo in lymphocytes and either the serum urate concentration or the 24 h urinary urate excretion on a purine-free diet. 6 Apart from those with recognized enzyme mutations, no subgroup of the gouty population has been demonstrated in whom isolated lymphocytes demonstrate an intrinsic abnormality of purine synthesis de novo.
摘要
  1. 研究了影响人淋巴细胞中嘌呤从头合成测量的变量,并建立了一种可靠的测量这些细胞中嘌呤合成活性的方法。2. 当生物合成途径的后续步骤被重氮丝氨酸阻断时,嘌呤从头合成以[14C]甲酸掺入α-N-甲酰甘氨酰胺核糖核苷酸的速率来衡量。在高磷酸盐浓度(25 mmol/l)的合成培养基中进行孵育。3. 多次从对照受试者和痛风患者,特别是那些尿尿酸值高提示尿酸产生过多的患者中获取淋巴细胞,测量嘌呤从头合成。4. 从每个个体在不同时间获取的淋巴细胞在嘌呤生物合成活性方面表现出相当大的差异。这种差异使得痛风患者和对照受试者获得的平均值之间没有差异。5. 在无嘌呤饮食条件下,淋巴细胞中嘌呤从头合成的平均活性与血清尿酸浓度或24小时尿尿酸排泄之间均未获得相关性。6. 除了那些具有已确认酶突变的患者外,尚未在痛风人群中证明有亚组的孤立淋巴细胞表现出嘌呤从头合成的内在异常。

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