Mineralocorticoid receptor blockade reduced oxidative stress in renal transplant recipients: A double-blind, randomized pilot study


Por: Ojeda-Cervantes, M, Barrera-Chimal, J, Alberu, J, Perez-Villalva, R, Morales-Buenrostro, LE, Bobadilla, NA

Publicada: 1 ene 2013
Categoría: Nephrology

Resumen:
Background: Previous experimental studies from our laboratory have demonstrated that aldosterone plays a central role in renal ischemic processes. This study was designed to evaluate the effect of mineralocorticoid receptor blockade in renal transplant recipients from living donors. Methods: 20 adult kidney transplant recipients from living donors were included in a double-blind, randomized, placebo-controlled clinical pilot study that compared spironolactone and placebo. Placebo or spironolactone (25 mg) was administered 1 day before and 3 days posttransplantation. Renal function and urinary kidney injury molecule-1, interleukin-18, and heat shock protein 72 as well as urinary hydrogen peroxide (H2O2) levels were quantified. Results: No significant differences were seen between the groups studied regarding age, gender, indication for kidney transplantation, residual renal function, renal replacement therapy, or warm and cold ischemia periods. In contrast, spironolactone administration significantly reduced the oxidative stress assessed by the urinary H2O2 excretion, in spite of no differences in renal function or reduction in tubular injury biomarkers. Conclusions: The findings of this exploratory study strongly suggest that aldosterone promotes oxidative stress and that the administration of spironolactone reduces the production of urinary H2O2 as a result of lesser formation of surrogate reactive oxygen species secondary to the ischemia-reperfusion phenomenon. Copyright © 2013 S. Karger AG, Basel.

Filiaciones:
Ojeda-Cervantes, M:
 Univ Nacl Autonoma Mexico, Dept Transplantat, Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Mexico City 04510, DF, Mexico

 Univ Nacl Autonoma Mexico, Dept Nephrol, Mexico City 04510, DF, Mexico

Barrera-Chimal, J:
 Univ Nacl Autonoma Mexico, Mol Physiol Unit, Inst Invest Biomed, Mexico City 04510, DF, Mexico

 Univ Nacl Autonoma Mexico, Dept Nephrol, Mexico City 04510, DF, Mexico

Alberu, J:
 Univ Nacl Autonoma Mexico, Dept Transplantat, Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Mexico City 04510, DF, Mexico

Perez-Villalva, R:
 Univ Nacl Autonoma Mexico, Mol Physiol Unit, Inst Invest Biomed, Mexico City 04510, DF, Mexico

 Univ Nacl Autonoma Mexico, Dept Nephrol, Mexico City 04510, DF, Mexico

Morales-Buenrostro, LE:
 Univ Nacl Autonoma Mexico, Dept Transplantat, Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Mexico City 04510, DF, Mexico

 Univ Nacl Autonoma Mexico, Dept Nephrol, Mexico City 04510, DF, Mexico

Bobadilla, NA:
 Univ Nacl Autonoma Mexico, Mol Physiol Unit, Inst Invest Biomed, Mexico City 04510, DF, Mexico

 Univ Nacl Autonoma Mexico, Dept Nephrol, Mexico City 04510, DF, Mexico
ISSN: 02508095
Editorial
KARGER, ALLSCHWILERSTRASSE 10, CH-4009 BASEL, SWITZERLAND, Suiza
Tipo de documento: Article
Volumen: 37 Número: 5
Páginas: 481-490
WOS Id: 000318703900010
ID de PubMed: 23635604

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