Clearance of transaminases during normothermic ex situ liver perfusion

PLoS One. 2019 Apr 24;14(4):e0215619. doi: 10.1371/journal.pone.0215619. eCollection 2019.

Abstract

Background: One of the most promising applications of liver normothermic machine perfusion (NMP) is the potential to directly assess graft viability and injury. In most NMP studies, perfusate transaminases are utilized as markers of graft injury. Our aim was to further elucidate the metabolism of transaminases by healthy porcine livers during NMP, specifically whether such livers could clear circuit perfusate transaminases.

Methods: A highly concentrated transaminase solution was prepared from homogenized liver, with an aspartate aminotransferase (AST) level of 107,427 U/L. Three livers in the treatment group were compared to three controls, during 48 hours of NMP. In the treatment group, the circuit perfusate was injected with the transaminase solution to artificially raise the AST level to a target of 7,500 U/L. Perfusate samples were taken at two-hour intervals and analyzed for biochemistry until NMP end. Graft oxygen consumption and vascular parameters were monitored.

Results: Compared to controls, treated perfusions demonstrated abrupt elevations in transaminase levels (p>0.0001) and lactate dehydrogenase (LDH) (p>0.0001), which decreased over time, but never to control baseline. Liver function, as demonstrated by lactate clearance and oxygen consumption was not different between groups. The treatment group demonstrated a higher portal vein resistance (p = 0.0003), however hepatic artery resistance was similar. Treated livers had higher bile production overall (p<0.0001).

Conclusions: Addition of high levels of transaminases and LDH to a healthy porcine liver during ex situ perfusion results in progressive clearance of these enzymes, suggesting preserved liver metabolism. Such tolerance tests may provide valuable indicators of prospective graft function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Humans
  • In Vitro Techniques
  • Liver / anatomy & histology
  • Liver / metabolism*
  • Liver / physiology
  • Liver Function Tests / methods
  • Liver Transplantation / methods
  • Metabolic Clearance Rate
  • Models, Animal
  • Organ Preservation / instrumentation
  • Organ Preservation / methods
  • Oxygen Consumption
  • Perfusion / instrumentation
  • Perfusion / methods
  • Portal Vein / physiology
  • Sus scrofa
  • Temperature
  • Transaminases / metabolism*
  • Vascular Resistance

Substances

  • Biomarkers
  • Transaminases

Grants and funding

MB is the recipient of the American Society of Transplant Surgeons (ASTS) 2015 Scientist Scholarship. AMJS holds a Tier-1 Canada Research Chair in Transplantation Surgery and Regenerative Medicine, and a Senior Clinical Scholarship from Alberta Innovates Healthcare Solutions. Funding from the Canadian Donation and Transplant Research Project (CDTRP) is gratefully acknowledged.