TY - JOUR
T1 - Evaluation of IGL-1 preservation solution using an orthotopic liver transplantation model
AU - Abdennebi, Hassen Ben
AU - Elrassi, Ziad
AU - Scoazec, Jean Yves
AU - Steghens, Jean Paul
AU - Ramella-Virieux, Silvina
AU - Boiliot, Olivier
PY - 2006/9/7
Y1 - 2006/9/7
N2 - Aim: To compare, in a pig liver transplantation model, the protective effect of UW with that of IGL-1, a high-sodium preservation solution containing polyethylene glycol (PEG) as an oncotic supply. Methods: All livers were harvested and grafted orthotopically according to standard techniques. The livers were washed out and preserved for 7 h in IGL-1 (n = 6) or in UW solution (n = 7) at 4°C. In a sham group (n = 4), the livers underwent a 60-min warm ischemia at 37°C. The hepatocellular injury was assessed in organ preservation solution washed out from the graft at the end of ischemic storage (before revascularization), and in serum 2 h after reperfusion and daily for up to 6 d. Results: Livers preserved in IGL-1 solution released markedly less AST than that preserved in the UW solution before and after revascularization (P < 0.05). Besides, the activity of creatine kinase-BB, a marker of sinusoidal lining cells injury, was higher in the UW group than in the IGL-1 group (P < 0.05). Histological results showed less necrotic regions in livers preserved in IGL-1 solution; however, no difference was observed for inflammation. Conclusion: IGL-1 liquid effectively protects parenchymal and non-parenchymal cells against preservation-reperfusion injuries.
AB - Aim: To compare, in a pig liver transplantation model, the protective effect of UW with that of IGL-1, a high-sodium preservation solution containing polyethylene glycol (PEG) as an oncotic supply. Methods: All livers were harvested and grafted orthotopically according to standard techniques. The livers were washed out and preserved for 7 h in IGL-1 (n = 6) or in UW solution (n = 7) at 4°C. In a sham group (n = 4), the livers underwent a 60-min warm ischemia at 37°C. The hepatocellular injury was assessed in organ preservation solution washed out from the graft at the end of ischemic storage (before revascularization), and in serum 2 h after reperfusion and daily for up to 6 d. Results: Livers preserved in IGL-1 solution released markedly less AST than that preserved in the UW solution before and after revascularization (P < 0.05). Besides, the activity of creatine kinase-BB, a marker of sinusoidal lining cells injury, was higher in the UW group than in the IGL-1 group (P < 0.05). Histological results showed less necrotic regions in livers preserved in IGL-1 solution; however, no difference was observed for inflammation. Conclusion: IGL-1 liquid effectively protects parenchymal and non-parenchymal cells against preservation-reperfusion injuries.
KW - Cold preservation
KW - IGL-1 liquid
KW - Liver transplantation
KW - Sinusoidal endothelial cells
KW - University of Wisconsin solution
UR - http://www.scopus.com/inward/record.url?scp=33749400154&partnerID=8YFLogxK
U2 - 10.3748/wjg.v12.i33.5326
DO - 10.3748/wjg.v12.i33.5326
M3 - Article
C2 - 16981262
AN - SCOPUS:33749400154
SN - 1007-9327
VL - 12
SP - 5326
EP - 5330
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
IS - 33
ER -