Odlind B, Beermann B
Clin Pharmacol Ther. 1980 Jun;27(6):784-90. doi: 10.1038/clpt.1980.111.
Continuous intravenous infusion of furosemide (8 mg/hr) to 6 healthy subjects induced an average diuresis at steady state of 667 +/- 144 ml/30 min (+/- SD) with a mean plasma concentration of furosemide of 623 +/- 209 ng/ml. The urinary output of Cl- was 50.4 +/- 7.5, of Na+ 47.7 +/- 8.7, and of K+ 5.4 +/- 0.6 mmole/30 min. Intravenous injection of probenecid (1 gm) raised the plasma furosemide level to a maximum of 1,584 +/- 151 ng/ml. Despite this, the urinary excretion of water, Cl-, Na+, and K+ decreased to 52%, 39%, 39%, and 52%, respectively, of control values. Probenecid greatly reduced the urinary excretion and renal clearance of furosemide. There was no or negative correlation between the plasma levels of furosemide and its diuretic and saluretic effects. The urinary excretion and renal clearance of the diuretic correlated positively with these effects. No effect of probenecid on protein binding of furosemide was detected. The findings show that the diuretic effects of furosemide depend on active tubular secretion of the drug and thus on its tubular fluid concentration.
对6名健康受试者持续静脉输注呋塞米(8毫克/小时),在稳态时平均利尿量为667±144毫升/30分钟(±标准差),呋塞米的平均血浆浓度为623±209纳克/毫升。氯的尿量为50.4±7.5、钠为47.7±8.7、钾为5.4±0.6毫摩尔/30分钟。静脉注射丙磺舒(1克)使呋塞米的血浆水平最高升至1584±151纳克/毫升。尽管如此,水、氯、钠和钾的尿排泄量分别降至对照值的52%、39%、39%和52%。丙磺舒大大降低了呋塞米的尿排泄和肾清除率。呋塞米的血浆水平与其利尿和促尿钠排泄作用之间无相关性或呈负相关。利尿剂的尿排泄和肾清除率与这些作用呈正相关。未检测到丙磺舒对呋塞米蛋白结合的影响。研究结果表明,呋塞米的利尿作用取决于药物的肾小管主动分泌,因此取决于其肾小管液浓度。