• Medientyp: E-Artikel
  • Titel: Biochemical, functional, and histopathologic characterization of lomustine-induced liver injury in dogs
  • Beteiligte: Dedeaux, Andrea M.; Flesner, Brian K.; Reinhart, Jennifer M.; Langohr, Ingeborg M.; Husnik, Roman; Geraci, Shawn N.; Taboada, Joseph; Rademacher, Nathalie; Thombs, Lori A.; Bryan, Jeffrey N.; Trepanier, Lauren A.; Boudreaux, Bonnie B.
  • Erschienen: American Veterinary Medical Association (AVMA), 2020
  • Erschienen in: American Journal of Veterinary Research, 81 (2020) 10, Seite 810-820
  • Sprache: Nicht zu entscheiden
  • DOI: 10.2460/ajvr.81.10.810
  • ISSN: 0002-9645
  • Schlagwörter: General Veterinary ; General Medicine
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: AbstractOBJECTIVETo characterize the biochemical, functional, and histopathologic changes associated with lomustine-induced liver injury in dogs.ANIMALSI0 healthy purpose-bred sexually intact female hounds.PROCEDURESDogs were randomly assigned to receive lomustine (approx 75 mg/m2, PO, q 21 d for 5 doses) alone (n = 5) or with prednisone (approx 1.5 mg/kg, PO, q 24 h for 12 weeks; 5). For each dog, a CBC, serum biochemical analysis, liver function testing, urinalysis, and ultrasonographic examination of the liver with acquisition of liver biopsy specimens were performed before and at predetermined times during and after lomustine administration. Results were compared between dogs that did and did not receive prednisone.RESULTS7 of the I0 dogs developed clinical signs of liver failure. For all dogs, serum alanine aminotransferase (ALT) and alkaline phosphatase (ALP) activities, bile acid concentrations, and liver histologic score increased and hepatic reduced glutathione content decreased over time. Peak serum ALT (r = 0.79) and ALP (r = 0.90) activities and bile acid concentration (r = 0.68) were positively correlated with the final histologic score. Prednisone did not appear to have a protective effect on histologic score.CONCLUSIONS AND CLINICAL RELEVANCEIn dogs, liver enzyme activities, particularly ALT and ALP activities, should be closely monitored during lomustine treatment and acute increases in those activities may warrant discontinuation of lomustine to mitigate liver injury. Nonspecific ultrasonographic findings and abnormal increases in liver function tests were not detected until the onset of clinical liver failure. Glutathione depletion may have a role in lomustine-induced hepatopathy and warrants further investigation.
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