Comparison between two warm ischemic models in experimental liver transplantation in pigs

被引:5
作者
Regueira, FM [1 ]
Espí, A [1 ]
Nwose, P [1 ]
Díez-Caballero, A [1 ]
Baixauli, J [1 ]
Rotellar, F [1 ]
Olea, J [1 ]
Pardo, F [1 ]
Hernández-Lizoain, JL [1 ]
Cienfuegos, JA [1 ]
机构
[1] Univ Clin Navarra, Dept Gen Surg, Pamplona 31008, Spain
关键词
D O I
10.1016/S0041-1345(03)00473-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Experimental models of warm ischemia in liver transplantation have been employed to study the mechanisms and treatment of ischemia reperfusion injury. Material. We compared a control group without (group A, n = 10) versus two models of warm ischemia of liver transplants in pigs: namely, occlusion of the hepatic artery and portal vein for 30 minutes (group B, n = 23) and extraction of the liver 60 minutes after cardiac arrest (group C, n = 5). Liver function tests, coagulation studies, and liver biopsies were performed during the first 24 hours post-liver transplant. Results. Clamping of the hepatic vasculature in group B produced a significant liver injury compared with the control group: elevation of the ALT and an abnormal 1-hour post-revascularization biopsy similar to that observed in the cardiac arrest group C. The transaminase levels were lower among group A animals (P < .05). But the hepatic synthetic functions as reflected in the protrombin time (PT) were not affected in group B versus group A. The alteration in PT with respect to the initial value was similar among group A and group B animals, which were significantly less than that in group C (P < .05). Conclusion. Occlusion of the hepatic artery and portal vein, a simple surgical maneuver, causes moderate damage to a liver graft but less alteration of hepatic synthetic function. Clamping of the hepatic vasculture obtains more long-term survivors after OLT than cardiac arrest.
引用
收藏
页码:1591 / 1593
页数:3
相关论文
共 11 条
[1]   PRINCIPLES OF SOLID-ORGAN PRESERVATION BY COLD-STORAGE [J].
BELZER, FO ;
SOUTHARD, JH .
TRANSPLANTATION, 1988, 45 (04) :673-676
[2]  
Calne RY, 1983, LIVER TRANSPLANTATIO
[3]  
CHUI C, 1987, TRANSPLANT P, V19, P1077
[4]   Influence of hepatic ischemia-reperfusion injury on tacrolimus acute renal toxicity in pigs [J].
Espí, A ;
Regueira, FM ;
Toledo, G ;
Díez-Caballero, A ;
Baixaulí, J ;
Hernández, JL ;
Roteller, F ;
Pardo, E ;
Cienfuegos, JA .
TRANSPLANTATION PROCEEDINGS, 2002, 34 (08) :3053-3056
[5]  
HERRERA J, 1982, TRANSPLANT P, V21, P2313
[6]   EVALUATION OF PROTOCOL BEFORE TRANSPLANTATION AND AFTER REPERFUSION BIOPSIES FROM HUMAN ORTHOTOPIC LIVER ALLOGRAFTS - CONSIDERATIONS OF PRESERVATION AND EARLY IMMUNOLOGICAL INJURY [J].
KAKIZOE, S ;
YANAGA, K ;
STARZL, TE ;
DEMETRIS, AJ .
HEPATOLOGY, 1990, 11 (06) :932-941
[7]   60-MINUTE NORMOTHERMIC LIVER ISCHEMIA IN RATS - EVIDENCE THAT ALLOPURINOL IMPROVES LIVER-CELL ENERGY-METABOLISM DURING REPERFUSION BUT THAT TIMING OF DRUG ADMINISTRATION IS IMPORTANT [J].
KARWINSKI, W ;
FARSTAD, M ;
ULVIK, R ;
SOREIDE, O .
TRANSPLANTATION, 1991, 52 (02) :231-234
[8]   PROBLEMS WITH ANIMAL-MODELS OF CHRONIC LIVER-DISEASE - SUGGESTIONS FOR IMPROVEMENT IN STANDARDIZATION [J].
MULLEN, KD ;
MCCULLOUGH, AJ .
HEPATOLOGY, 1989, 9 (03) :500-503
[9]   Effect of treatment with tranexamic acid on complement activation and ischemia reperfusion in liver transplantation in pigs [J].
Nwose, PE ;
Regueira, FM ;
Sierra, A ;
Diez-Caballero, A ;
Hernández, JL ;
Pardo, F ;
Cienfuegos, JA .
TRANSPLANTATION PROCEEDINGS, 1999, 31 (06) :2431-2432
[10]   Ischemic damage prevention by N-acetylcysteine treatment of the donor before orthotopic liver transplantation [J].
Regueira, FM ;
Hernández, JL ;
Sola, I ;
Cienfuegos, JA ;
Pardo, F ;
Díez-Caballero, A ;
Sierra, A ;
Nwose, E ;
Espí, A ;
Baixaúli, J ;
Rotellar, F .
TRANSPLANTATION PROCEEDINGS, 1997, 29 (08) :3347-3349