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Decreased survival in rat liver transplantation with extended cold preservation: Role of portal vein clamping time
Author(s) -
Urata Koichi,
Nguyen Bich,
Brault Antoine,
Lavoie Joël,
Rocheleau Bernard,
Huet PierreMichel
Publication year - 1998
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.510280211
Subject(s) - medicine , liver transplantation , transplantation , ischemia , clamping , viaspan , cold storage , hepatocyte , perfusion , surgery , biology , biochemistry , mechanical engineering , horticulture , engineering , in vitro
Primary liver graft dysfunction is currently related to cold ischemia‐reperfusion injury, although a wide survival range has been reported using 24‐hour preservation in cold University of Wisconsin (UW) solution. We hypothesized that the portal vein clamping time (PVCT) played a more important role than cold preservation injury in the postoperative outcome. Rat liver transplantation was performed using different clamping times after 24‐hour cold ischemia in the UW solution. Survival rates, plasma tumor necrosis factor (TNF), and nitrate/nitrite levels were examined. Subsequently, the effect of clamping time was evaluated on hepatocyte and sinusoidal endothelial cell (SEC) function using isolated perfused livers. Survival rate was directly related to clamping time length. Marked increases in TNF and nitrate/nitrite levels were found after surgery, particularly after long clamping times. In perfusion studies, the SEC function was already markedly altered after preservation alone and was not further modified by transplantation. By contrast, the hepatocyte function was moderately altered after transplantation, irrespective of clamping times, even when rats operated with long clamping times were in terminal conditions. In rats, 24‐hour preservation in cold UW solution is not a severely compromising condition leading to primary liver nonfunction. Long PVCTs are associated with an endotoxemia‐like syndrome more related to a warm intestinal ischemia than to cold ischemia injury of the liver.