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Research ArticleArticle

Role of Plasma Protein Binding on Renal Metabolism and Dynamics of Furosemide in the Rabbit

Vincent Pichette, David Geadah and Patrick du Souich
Drug Metabolism and Disposition January 1999, 27 (1) 81-85;
Vincent Pichette
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David Geadah
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Patrick du Souich
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Abstract

To investigate the influence of furosemide plasma protein binding on its kinetics and dynamics, the kinetics of furosemide was studied in the presence of a protein binding displacer, warfarin, and in hypoalbuminemic rabbits. Compared with controls, in anesthetized rabbits pretreated with warfarin, the unbound fraction of furosemide increased from 1.8 ± 0.4% to 7.0 ± 0.4% (p < .001), and its metabolic clearance increased by 30%, whereas furosemide urinary excretion decreased by 48% (p < .05). Experiments in nephrectomized rabbits showed that the increase in metabolic clearance was secondary to an increase in its renal metabolic clearance (p < .05). Compared with controls, in warfarin pretreated rabbits, sodium excretion and diuresis were decreased by 30% (p < .05). However, when furosemide was injected mixed with albumin, warfarin-induced kinetic and dynamic alterations of furosemide were reversed. Compared with control rabbits, in conscious hypoalbuminemic rabbits, furosemide unbound fraction was enhanced from 1.2 ± 0.1% to 5.5 ± 0.5% (p < .001), and its urinary excretion, diuresis, and sodium excretion were reduced by 22% (p < .05). The administration of warfarin to hypoalbuminemic rabbits further increased the fraction of unbound furosemide, and diminished its urinary excretion and diuretic effect. In conclusion, 1) binding of furosemide to plasma proteins, and not albumin per se, facilitates its renal secretion and pharmacological response; 2) the decrease in furosemide binding, secondary to drug displacement and/or hypoalbuminemia, can be a cause of resistance to the diuretic; and 3) when furosemide binding is decreased, the administration of furosemide mixed with albumin enhances its renal secretion and diuretic effect.

Footnotes

  • Send reprint requests to: Patrick du Souich, Department of Pharmacology, Faculty of Medicine, University of Montréal, Box 6128, Station “Centre Ville”, Montréal, Québec Canada H3C 3J7. E-mail: dusouicp{at}ERE.UMontreal.CA

  • This work was supported by the Medical Research Council of Canada (Grant MT-10874). Part of this work has been presented at the 30th annual meeting of the American Society of Nephrology in San Antonio.

  • Abbreviations used are::
    GFR
    glomerular filtration rate
    AUC0–60 orAUC0–150, area under its plasma concentration-time curve
    Clu, urinary clearance of furosemide
    • Received March 30, 1998.
    • Accepted August 13, 1998.
  • The American Society for Pharmacology and Experimental Therapeutics
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Drug Metabolism and Disposition: 27 (1)
Drug Metabolism and Disposition
Vol. 27, Issue 1
1 Jan 1999
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Research ArticleArticle

Role of Plasma Protein Binding on Renal Metabolism and Dynamics of Furosemide in the Rabbit

Vincent Pichette, David Geadah and Patrick du Souich
Drug Metabolism and Disposition January 1, 1999, 27 (1) 81-85;

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Research ArticleArticle

Role of Plasma Protein Binding on Renal Metabolism and Dynamics of Furosemide in the Rabbit

Vincent Pichette, David Geadah and Patrick du Souich
Drug Metabolism and Disposition January 1, 1999, 27 (1) 81-85;
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