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Warfarin-Related Nephropathy Modeled by Nephron Reduction and Excessive Anticoagulation
Author(s) -
Kyle Ware,
Polina Brodsky,
Anjali A. Satoskar,
Tibor Nádasdy,
Gyongyi Nadasdy,
Haifeng Wu,
Brad H. Rovin,
Udayan Bhatt,
Jon Von Visger,
Lee A. Hebert,
Sergey V. Brodsky
Publication year - 2011
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.2010101110
Subject(s) - medicine , nephron , warfarin , nephropathy , acute kidney injury , kidney disease , creatinine , pathogenesis , nephrectomy , urology , acute tubular necrosis , kidney , renal function , gastroenterology , endocrinology , diabetes mellitus , atrial fibrillation
An acute increase in international normalized ratio (INR) to >3.0 in patients with chronic kidney disease (CKD) can associate with an unexplained acute increase in serum creatinine and accelerated progression of CKD. A subset of these patients have renal tubular obstruction by casts of red blood cells, presumably the dominant mechanism of the acute kidney injury described as warfarin-related nephropathy. Here, we developed an animal model of this acute kidney injury that is based on the 5/6-nephrectomy model to aid future investigation of the pathogenesis of this condition. We found that acute excessive anticoagulation with brodifacoum ("superwarfarin") increased serum creatinine levels and hematuria in 5/6-nephrectomized rats but not in controls. In addition, morphologic findings in 5/6-nephrectomized rats included glomerular hemorrhage, occlusive red blood cell casts, and acute tubular injury, similar to the biopsy findings among affected patients. Furthermore, in the rat model, we observed an increase in apoptosis of glomerular endothelial cells. In summary, the 5/6-nephrectomy model combined with excessive anticoagulation may be a useful tool to study the pathogenesis of warfarin-related nephropathy.

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