Cold preservation injury in rat liver: effect of liposomally-entrapped adenosine triphosphate

J Hepatol. 2000 Jul;33(1):68-75. doi: 10.1016/s0168-8278(00)80161-0.

Abstract

Background/aims: Energy charge and capacity for adenosine triphosphate (ATP) synthesis have been demonstrated to play a major role in the maintenance of organ function after liver preservation for transplantation. The aim of this study was to evaluate whether a supply of liposomally-entrapped ATP during preservation could improve the energy state and metabolism of cold-stored rat liver.

Methods: In the first set of experiments, the uptake of ATP-containing liposomes and their effects on hepatic viability were determined in isolated perfused unstored rat liver. In the second set of experiments, rat livers were preserved for 18 h at 4 degrees C in UW solution in the presence of these liposomes, and effects on energy state, cell volume and metabolism were evaluated. In each part, data were compared with adequate control, unloaded liposome-treated, and free ATP-treated groups (n=6 in each group).

Results: In non-stored livers, ATP-containing liposomes were taken up by the liver; they did not alter hepatic viability and induced a decrease in energy substrate consumption (glucose and amino acids), and an improvement in intrahepatic ATP content (+23% vs. Control). Addition of liposomally-entrapped ATP during cold storage produced a significant attenuation of the decrease in hepatic ATP content (Lip ATP 2: 524+/-45 vs. Control 2: 364+/-106 nmol/g; p<0.05), and induced, during reperfusion, a decrease in proteolysis associated with an increase in cell volume compared with the other groups (Lip ATP 2: 633+/-63 vs. Control 2: 532+/-38, Unloaded Lip 2: 483+/-55 and Free ATP 2: 500+/-29 microl/g; p<0.01).

Conclusions: These data indicate that liposomally-entrapped ATP represents an effective means to improve liver graft energy state and function. The decrease in protein degradation may be related to the modification of cell volume.

MeSH terms

  • Adenosine Triphosphate / administration & dosage*
  • Adenosine Triphosphate / therapeutic use
  • Animals
  • Cryopreservation*
  • Drug Carriers
  • Energy Metabolism / drug effects
  • In Vitro Techniques
  • Liposomes
  • Liver / drug effects
  • Liver / injuries*
  • Liver / pathology
  • Liver / physiopathology
  • Male
  • Peptide Hydrolases / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reference Values
  • Tissue Survival
  • Wounds and Injuries / drug therapy*
  • Wounds and Injuries / etiology*
  • Wounds and Injuries / pathology
  • Wounds and Injuries / physiopathology

Substances

  • Drug Carriers
  • Liposomes
  • Adenosine Triphosphate
  • Peptide Hydrolases