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Novel genomic biomarkers for acute gentamicin nephrotoxicity in dog

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DOI: 10.4236/ojmip.2013.33018    3,566 Downloads   6,531 Views   Citations

ABSTRACT

Objectives: Novel biomarkers indicative of drug-induced kidney injury (DIKI) in dogs would have significant application in preclinical drug development. We conducted a feasibility study to identify genomic expression profiles for monitoring progressive, acute DIKI in dogs. Materials and Methods: Animals were intramuscularly administered either 0.9% physiological saline or gentamicin (40 mg/kg/day) for 10 consecutive days and euthanized on day 11. Serum and urine samples were collected at various time points and kidney samples were collected at necropsy for biomarker measurements. Results: Acute gentamicin-induced renal histopathology changes were localized to the proximal convoluted tubules and characterized as slight-to-marked, diffuse cortical-medullary tubular epithelial degeneration/necrosis. Serum creatinine (sCr) and blood urea nitrogen (BUN) elevations suggestive of mild renal dysfunction were first observed on days 7 to 8. Gentamicin-induced increased urinary kidney injury molecule-1 (KIM-1) mRNA was observed on day 6 preceding detectable elevations of sCr and/or BUN. Increased urinary KIM-1 mRNA correlated with multifocal KIM-1 immunostaining in the corticomedullary tubular epithelial cells. Microarray analysis revealed changes in additional mRNA expression products detected in urine and/or kidney that should be further investigated for use as potential biomarkers for acute gentamicin related nephrotoxicity in dogs. Conclusion: These findings suggested the utility of non-invasive urinary genomic parameters for monitoring acute DIKI in dogs.

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

McDuffie, J. , Gao, J. , Ma, J. , La, D. , Bittner, A. , Sonee, M. , Wagoner, M. and Snook, S. (2013) Novel genomic biomarkers for acute gentamicin nephrotoxicity in dog. Open Journal of Molecular and Integrative Physiology, 3, 125-133. doi: 10.4236/ojmip.2013.33018.

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