Akaoka I, Nishizawa T, Yano E, Kamtani N, Nishida Y, Sasaki S
J Rheumatol. 1977 Spring;4(1):86-94.
Renal urate excretion was studied in two familial, one suspected familial, and two isolated cases of hypouricemia due to a renal defect. All had very low plasma urate concentrations. In four cases, the urate clearances were approximately the same as the creatinine clearances, and in one case reduced to about one-third. In all cases the urate clearances were minimally diminished by both pyrazinamide and probenecid. This renal response to the drugs is probably due to and isolated tubular defect in the reabsorptive transport mechanism of urate. Following intravenous administration of uric acid, one patient excreted uric acid in the urine more rapidly than a normal subject. In this patient, uric acid secretion from renal tubules was clearly demonstrated during infusion of uric acid. In de novo synthesis of purine, no definite abnormalities were found by incorporation of glycine-15N to uric acid.
对两例家族性、一例疑似家族性以及两例因肾脏缺陷导致的特发性低尿酸血症患者的肾脏尿酸排泄情况进行了研究。所有患者的血浆尿酸浓度都非常低。在四例患者中,尿酸清除率与肌酐清除率大致相同,一例患者的尿酸清除率降至约三分之一。在所有病例中,吡嗪酰胺和丙磺舒对尿酸清除率的降低作用均微乎其微。肾脏对这些药物的反应可能是由于尿酸重吸收转运机制中存在孤立的肾小管缺陷。静脉注射尿酸后,一名患者尿液中尿酸的排泄速度比正常受试者更快。在该患者输注尿酸期间,清楚地证明了肾小管能分泌尿酸。在嘌呤的从头合成过程中,通过将甘氨酸 - 15N掺入尿酸未发现明确异常。