Villeneuve J P, Verbeeck R K, Wilkinson G R, Branch R A
Clin Pharmacol Ther. 1986 Jul;40(1):14-20. doi: 10.1038/clpt.1986.132.
Factors that influence intersubject variability in response to furosemide have been investigated in normal subjects and patients with cirrhosis. Furosemide pharmacokinetics and pharmacodynamics were measured in eight normal subjects and 14 patients with cirrhosis, eight of whom were resistant to diuretic therapy. Furosemide renal clearance decreased in proportion to creatinine clearance, whereas nonrenal clearance and volume of distribution were unchanged. These pharmacokinetic changes were, however, minimal and resulted in an only marginal alteration in the plasma concentration-time curve. The maximal rate of urinary sodium excretion decreased with reductions in creatinine clearance (r = 0.77). However, the extent of reduction in urinary excretion of sodium was proportionally greater than the reduction in creatinine clearance, whereas the rate of urinary furosemide excretion required to achieve 50% of maximal response did not change. Furosemide's pharmacokinetics were not, therefore, appreciably altered by cirrhosis. However, cirrhosis was associated with a reduction in pharmacodynamic response to this diuretic.
在正常受试者和肝硬化患者中,对影响速尿反应个体间变异性的因素进行了研究。在8名正常受试者和14名肝硬化患者中测量了速尿的药代动力学和药效学,其中8名患者对利尿治疗有抵抗性。速尿肾清除率与肌酐清除率成比例下降,而非肾清除率和分布容积不变。然而,这些药代动力学变化很小,仅导致血浆浓度-时间曲线有轻微改变。尿钠排泄的最大速率随肌酐清除率的降低而降低(r = 0.77)。然而,尿钠排泄减少的程度按比例大于肌酐清除率的降低,而达到最大反应50%所需的速尿尿排泄速率没有变化。因此,肝硬化并未明显改变速尿的药代动力学。然而,肝硬化与对这种利尿剂的药效学反应降低有关。