Role of purines on hepatic ischemia-reperfusion lesions in rabbit

Transplant Proc. 2009 Apr;41(3):807-11. doi: 10.1016/j.transproceed.2009.01.057.

Abstract

In this work, we evaluate the effects of adenosine 5' triphosphate (ATP) on hepatic lesions caused by ischemia/reperfusion (I/R) in liver rabbit. Rabbits were pretreated with ATP (15 mg/kg IV) or saline solution 0.9% (SS), before the hepatic I/R procedure. We evaluated the effects of ATP on hepatic injury before and after I/R. The 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 these changes were attenuate by ATP treatment before the hepatic I/R procedure. These results suggested that ATP exerted protective effects on hepatic I/R lesions in the rabbit. This ATP effect may be related to improved energy metabolism during reperfusion in ischemic livers protecting against functional damage of cellular and subcellular membranes during lipid peroxidation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / therapeutic use
  • Alanine Transaminase / drug effects
  • Alanine Transaminase / metabolism
  • Animals
  • Aspartate Aminotransferases / drug effects
  • Aspartate Aminotransferases / metabolism
  • Ischemia / physiopathology
  • L-Lactate Dehydrogenase / drug effects
  • L-Lactate Dehydrogenase / metabolism
  • Liver / drug effects
  • Liver / physiopathology
  • Liver Diseases / physiopathology*
  • Liver Diseases / prevention & control
  • Male
  • Mitochondria, Liver / drug effects
  • Mitochondria, Liver / metabolism
  • Purines / metabolism*
  • Rabbits
  • Reperfusion Injury / physiopathology*
  • Reperfusion Injury / prevention & control

Substances

  • Purines
  • Adenosine Triphosphate
  • L-Lactate Dehydrogenase
  • Aspartate Aminotransferases
  • Alanine Transaminase