Machine perfusion at 20°C reduces preservation damage to livers from non-heart beating donors
Male
LIVER
610
NON-HEART BEATING DONORS
612
03 medical and health sciences
Adenosine Triphosphate
0302 clinical medicine
Glutamate Dehydrogenase
Animals
Bile
Aspartate Aminotransferases
Sulfhydryl Compounds
Rats, Wistar
Glutathione Disulfide
L-Lactate Dehydrogenase
Organ Preservation
Glutathione
Portal Pressure
Tissue Donors
Rats
Cold Temperature
Perfusion
MACHINE PERFUSION PRESERVATION
Liver
Reperfusion
Glycogen
DOI:
10.1016/j.cryobiol.2011.02.004
Publication Date:
2011-02-11T09:27:10Z
AUTHORS (10)
ABSTRACT
We previously reported that machine perfusion (MP) performed at 20°C enhanced the preservation of steatotic rat livers. Here, we tested whether rat livers retrieved 30 min after cardiac arrest (NHBDs) were better protected by MP at 20°C than with cold storage. We compared the recovery of livers from NHBDs with organs obtained from heart beating donors (HBDs) preserved by cold storage. MP technique: livers were perfused for 6h with UW-G modified at 20°C. Cold storage: livers were perfused in situ and preserved with UW solution at 4°C for 6h. Both MP and cold storage preserved livers were reperfused with Krebs-Heinselet buffer (2h at 37°C). AST and LDH release and mitochondrial glutamate dehydrogenase (GDH) levels were evaluated. Parameters assessed included: bile production and biliary enzymes; tissue ATP; reduced and oxidized glutathione (GSH/GSSG); protein-SH group concentration. Livers preserved by MP at 20°C showed significantly lower hepatic damage at the end of reperfusion compared with cold storage. GDH release was significantly reduced and bile production, ATP levels, GSH/GSSG and protein-SH groups were higher in livers preserved by MP at 20°C than with cold storage. The best preserved morphology and high glycogen content was obtained with livers submitted to MP at 20°C. Liver recovery using MP at 20°C was comparable to recovery with HBDs. MP at 20°C improves cell survival and gives a better-quality of preservation for livers obtained from NHBDs and may provide a new method for the successful utilization of marginal livers.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (42)
CITATIONS (41)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....