Yamamoto T, Moriwaki Y, Takahashi S, Tsutsumi Z, Hada T
Third Department of Internal Medicine, Hyogo College of Medicine, Japan.
Metabolism. 2001 Feb;50(2):241-5. doi: 10.1053/meta.2001.19489.
To examine whether furosemide affects the plasma concentration and urinary excretion of purine bases and oxypurinol, we administered allopurinol (300 mg) orally to 6 healthy subjects and then administered furosemide (20 mg) intravenously 10 hours later. Furosemide (20 mg) decreased the urinary excretion of uric acid by 40% (P < .01), oxypurinol by 39% (P < .05), and xanthine by 43% (P < .05) and the fractional clearance of uric acid by 45% (P < .01) and oxypurinol by 34% (P < .05) when measured 1 to 2 hours after administration. Moreover, furosemide increased the plasma concentration of uric acid by 6% at 1.5 hours after administration. These results indicate that furosemide may decrease the urinary excretion of uric acid and oxypurinol by acting on their common renal transport pathway(s). In addition, it is suggested that the effect of furosemide on oxypurinol is clinically important, since the hypouricemic effect of allopurinol may become more potent as a result.
为了研究呋塞米是否会影响嘌呤碱和氧嘌呤醇的血浆浓度及尿排泄,我们对6名健康受试者口服给予别嘌醇(300mg),然后在10小时后静脉给予呋塞米(20mg)。给药后1至2小时测量发现,呋塞米(20mg)使尿酸尿排泄减少40%(P <.01),氧嘌呤醇减少39%(P <.05),黄嘌呤减少43%(P <.05),尿酸的分数清除率减少45%(P <.01),氧嘌呤醇减少34%(P <.05)。此外,呋塞米在给药后1.5小时使尿酸血浆浓度升高6%。这些结果表明,呋塞米可能通过作用于尿酸和氧嘌呤醇共同的肾脏转运途径来减少它们的尿排泄。此外,由于别嘌醇的降尿酸作用可能因此变得更强,提示呋塞米对氧嘌呤醇的影响具有临床重要性。