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Transplant Proc ; 41(3): 820-3, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19376361

ABSTRACT

In this work, we evaluated the effects of allopurinol (ALO), an inhibitor of xanthine oxidase (XO), on hepatic lesions caused by ischemia/reperfusion (I/R) in the rabbit liver. Rabbits were pretreated with ALO (10 mg/kg IV) or saline solution 0.9% before the hepatic I/R procedure. The effects of ALO on hepatic injury were evaluated before and after I/R. A standard, warm hepatic I/R procedure caused profound acute liver injury, as indicated by elevated serum aspartate aminotransferase, alanine aminotransferase, and lactic dehydrogenase levels, as well as a high apoptotic cell count. All of these changes were reversed by the administration of ALO before the hepatic I/R procedure. In conclusion, ALO exerted protective effects on hepatic I/R lesions. This protective effect of ALO was probably associated with blocking the generation of superoxide anions during the hepatic I/R procedure by inhibiting XO activity.


Subject(s)
Allopurinol/therapeutic use , Liver Diseases/prevention & control , Reperfusion Injury/prevention & control , Alanine Transaminase/blood , Alanine Transaminase/drug effects , Animals , Aspartate Aminotransferases/blood , Aspartate Aminotransferases/drug effects , Enzyme Inhibitors/therapeutic use , L-Lactate Dehydrogenase/blood , L-Lactate Dehydrogenase/drug effects , Male , Rabbits , Xanthine Oxidase/antagonists & inhibitors
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