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在一名痛风患者中给予三甘氨酰加压素后丙磺舒促尿酸排泄作用的恢复。

Restoration of the uricosuric effect of probenecid after triglycylvasopressine administration in a gouty patient.

作者信息

Decaux G, Soupart A, Musch W, Hannotier P, Prospert F

机构信息

Hôpital Universitaire Erasme, Université Libre de Bruxelles, Belgium.

出版信息

Clin Nephrol. 1998 Oct;50(4):262-5.

PMID:9799074
Abstract

A 35-year-old patient with severe gout and mild renal insufficiency presented very low urinary urate excretion. Volume expansion induced by fludrocortisone combined or not with a uricosuric drug (Benzbromarone) was unable to significantly increase his urate excretion. A combined Probenecid (PB) and Pyrazinamide (PZA) test was performed. These drugs being considered to affect renal tubular reabsorption or secretion. No significant modification of uric acid fractional excretion (FE.uric acid) was observed after PB and PZA. When the same test was performed after the administration of Triglycyl-lysine vasopressine (TGLV), a potent V1 receptor stimulator, we observed a three fold increase in FE.uric acid after PB intake (from 6 to 18%) followed by a decrease after PZA (from 18 to 5.6%). When TGLV was administered alone their was no significant modification of uric acid fractional excretion. We propose that TGLV decrease proximal tubular urate reabsorption that could only be detected when postsecretory reabsorption is blocked by an uricosuric drug.

摘要

一名35岁患有严重痛风和轻度肾功能不全的患者尿尿酸排泄极低。使用氟氢可的松单独或联合促尿酸排泄药物(苯溴马隆)诱导的容量扩张均未能显著增加其尿酸排泄。进行了丙磺舒(PB)和吡嗪酰胺(PZA)联合试验。这些药物被认为会影响肾小管重吸收或分泌。给予PB和PZA后,未观察到尿酸排泄分数(FE.尿酸)有显著改变。当给予强效V1受体刺激剂三甘氨酰赖氨酸加压素(TGLV)后进行相同试验时,我们观察到摄入PB后FE.尿酸增加了三倍(从6%增至18%),随后给予PZA后下降(从18%降至5.6%)。单独给予TGLV时,尿酸排泄分数无显著改变。我们提出,TGLV降低近端肾小管尿酸重吸收,而这只有在促尿酸排泄药物阻断分泌后重吸收时才能被检测到。

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