Strain-related Differences in Urine Composition of Male Rats of Potential Relevance to Urolithiasis

Author:

Tannehill-Gregg Sarah H.1,Dominick Mark A.1,Reisinger Amy J.1,Moehlenkamp Jeffrey D.1,Waites C. Robbie12,Stock David A.3,Sanderson Thomas P.1,Cohen Samuel M.4,Arnold Lora L.4,Schilling Beth E.1

Affiliation:

1. Bristol-Myers Squibb Research & Development, Department of Drug Safety Evaluation, Mount Vernon, Indiana, USA

2. SABIC Innovative Plastics, Mount Vernon, Indiana, USA

3. Bristol-Myers Squibb Research & Development, Department of Global Biometric Sciences, Wallingford, Connecticut, USA

4. Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, USA

Abstract

In carcinogenicity studies with PPAR γ and α/γ agonists, urinary bladder tumors have been reported in Harlan Sprague-Dawley (HSD) and Charles River Sprague-Dawley (SD) but not Wistar (WI) rats, with urolithiasis purported to be the inciting event. In two 3-month studies, the authors investigated strain-related differences in urine composition by sampling urine multiple times daily. Urine pH, electrolytes, creatinine, protein, citrate and oxalate levels, and serum citrate were assessed; urine sediment was analyzed by scanning electron microscopy and energy dispersive x-ray spectroscopy. HSD rats had significantly higher urine calcium than SD or WI rats, primarily as calcium phosphate-containing precipitate. When compared to SD rats, HSD rats had lower urine volume, higher urine protein, and a comparable (week 4) to lower (week 13) burden of MgNH4PO4 aggregates. Relative to WI rats, HSD rats had higher urine protein and magnesium and lower serum and urine citrate. Overall, the susceptibility to urolithiasis in male rats was HSD > SD > WI; this was likely due to strain-related differences in the amount of urine protein (a nidus for crystal formation), lithogenic ions, citrate (an inhibitor of lithogenesis), and/or volume. Strain-related differences in urine composition need to be considered when interpreting the outcome of studies with compounds that alter urine composition.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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