URINARY ENZYME EVALUATION OF NEPHROTOXICITY IN THE DOG

Authors
Citation
Fas. Clemo, URINARY ENZYME EVALUATION OF NEPHROTOXICITY IN THE DOG, Toxicologic pathology, 26(1), 1998, pp. 29-32
Citations number
28
Categorie Soggetti
Toxicology,Pathology
Journal title
ISSN journal
01926233
Volume
26
Issue
1
Year of publication
1998
Pages
29 - 32
Database
ISI
SICI code
0192-6233(1998)26:1<29:UEEONI>2.0.ZU;2-M
Abstract
Over the past 20 yr, increased attention has been directed toward eval uation of urinary enzymes as markers of nephrotoxicity in dogs because the technique is noninvasive and considered to be more sensitive than the more commonly used conventional tests of renal function. Urinary enzymes also have the potential of determining the primary site of ren al damage because different sections of the nephron have a characteris tic complement of enzymes. In dogs, increases in brush border enzymes, including gamma-glutamyl transferase and alkaline phosphatase, have b een associated with renal proximal tubular damage, while increases in N-acetyl-beta-D-glucosaminidase have been observed in the early stage of renal papillary necrosis. Urinary enzymes have been particularly us eful in detection of acute renal damage in dogs, Specifically tubular damage; however, their corresponding value in providing information ab out chronic renal damage remains to be established. Although elevation of certain enzymes appears to be a relatively sensitive measure of ne phrotoxicity in the dog, there is no current agreement regarding which enzyme assays are the most appropriate for routine use in safety asse ssment studies. In addition, elevation of a single enzyme is of limite d diagnostic value in detection of renal damage because spurious incre ases in urinary enzymes sometimes occur in normal dogs. Therefore, if one wishes to conduct special assessment of nephrotoxicity in dogs, ev aluation of several enzymes at multiple time points is needed to compe nsate for normal enzyme variation and to identify potential anatomic s ite selectivity of the toxin.