| Literature DB >> 32012434 |
Tom Darius1,2, Martial Vergauwen2, Thomas Smith3, Isabelle Gerin4, Virginie Joris5, Matteo Mueller6, Selda Aydin7, Xavier Muller6, Andrea Schlegel8, Jay Nath9, Christian Ludwig3, Chantal Dessy5, Marie-Christine Many10, Guido Bommer4, Philipp Dutkowski6, Pierre Gianello2, Michel Mourad1,2.
Abstract
With oxygenation proposed as a resuscitative measure during hypothermic models of preservation, the aim of this study was to evaluate the optimal start time of oxygenation during continuous hypothermic machine perfusion (HMP). In this porcine ischemia-reperfusion autotransplant model, the left kidney of a ±40 kg pig was exposed to 30 minutes of warm ischemia prior to 22 hours of HMP and autotransplantation. Kidneys were randomized to receive 2 hours of oxygenation during HMP either at the start (n = 6), or end of the perfusion (n = 5) and outcomes were compared to standard, nonoxygenated HMP (n = 6) and continuous oxygenated HMP (n = 8). The brief initial and continuous oxygenated HMP groups were associated with superior graft recovery compared to either standard, nonoxygenated HMP or kidneys oxygenated at the end of HMP. This correlated with significant metabolic differences in perfusate (eg, lactate, succinate, flavin mononucleotide) and tissues (eg, succinate, adenosine triphosphate, hypoxia-inducible factor-1α, nuclear factor erythroid 2-related factor 2) suggesting superior mitochondrial preservation with initial oxygenation. Brief initial O2 uploading during HMP at procurement site might be an easy and effective preservation strategy to maintain aerobic metabolism, protect mitochondria, and achieve an improved early renal graft function compared with standard HMP or oxygen supply shortly at the end of HMP preservation.Entities:
Keywords: animal models: porcine; autotransplantation; ischemia-reperfusion injury (IRI); kidney (allograft) function/dysfunction; kidney transplantation/nephrology; organ perfusion and preservation; organ procurement and allocation; translational research/science
Mesh:
Year: 2020 PMID: 32012434 DOI: 10.1111/ajt.15800
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086