Hepatic tyrosine aminotransferase and glucocorticoid abuse in meat cattle

J Vet Pharmacol Ther. 2012 Dec;35(6):596-603. doi: 10.1111/j.1365-2885.2012.01378.x. Epub 2012 Feb 29.

Abstract

Besides being extensively applied as therapeutical remedies, glucocorticoids (GCs) - most notably dexamethasone or prednisolone - are also illegally used in livestock for growth-promoting purposes. This study was designed to assess the suitability of liver tyrosine aminotransferase (TAT), a gluconeogenic enzyme known to be induced by GCs, to act as a reliable candidate biomarker to screen for GC abuse in cattle. Enzyme activity was measured spectrophotometrically in liver cytosols or in cell extracts, and TAT gene expression was determined by real-time PCR. Compared with untreated veal calves, a notable scatter (20-fold) and much higher median values (3-fold) characterized TAT specific activity in liver samples from commercially farmed veal calves. A time-related increase in both enzyme activity and gene expression was detected in rat hepatoma cell lines treated with dexamethasone concentrations (10(-8) or 10(-9) m) in the range of those recorded in noncompliant samples from EU official controls. In experimental studies in which finishing bulls were administered GCs at growth-promoting dosages, however, no such changes were recorded in dexamethasone-treated animals; a statistically significant rise in liver TAT activity (+95%) only occurred in prednisolone-treated bulls. Although further research is needed to characterize the GC-mediated response in cattle liver, TAT does not appear to be a specific and sensitive biomarker of GC abuse in the bovine species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • Carcinoma, Hepatocellular / metabolism
  • Cattle / metabolism*
  • Cell Line, Tumor
  • Dexamethasone
  • Gene Expression Regulation, Enzymologic
  • Glucocorticoids / administration & dosage*
  • Glucocorticoids / pharmacology
  • Liver / drug effects
  • Liver / enzymology*
  • Liver Neoplasms / metabolism
  • Male
  • RNA / genetics
  • RNA / metabolism
  • Rats
  • Real-Time Polymerase Chain Reaction
  • Substance Abuse Detection / methods
  • Substance Abuse Detection / veterinary*
  • Tyrosine Transaminase / metabolism*

Substances

  • Biomarkers
  • Glucocorticoids
  • RNA
  • Dexamethasone
  • Tyrosine Transaminase