Assessment of the AMC-bioartificial liver in the anhepatic pig

被引:48
作者
Sosef, MN [1 ]
Abrahamse, LSL [1 ]
van de Kerkhove, MP [1 ]
Hartman, R [1 ]
Chamuleau, RAFM [1 ]
van Gulik, TM [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Surg, Surg Lab TWO 1 155, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1097/00007890-200201270-00009
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. The anhepatic pig model was used to evaluate a bioartificial liver developed in our institution (AMC-BAL). The bioartificial liver is based on oxygenated plasma perfusion of porcine hepatocytes attached to a polyester matrix. Methods. Pigs (n=15) underwent total hepatectomy with restoration of caval continuity using a polyethylene, three-way prosthesis. In group 1, pigs received limited intensive care under continuation of general anesthesia (n=5). Group II pigs (n=5) underwent, in addition, extracorporeal plasma perfusion of an AMC-BAL without hepatocytes (device control group). In group III (n=5), plasma perfusion occurred with an AMC-BAL loaded with autologous hepatocytes. Groups II and III were connected to the extracorporeal system 24 hr after hepatectomy, for a period of 24 hr. The main outcome parameters were as follows: survival time, liver enzymes (aspartate aminotransferase, alanine aminotransferase), blood ammonia, and total/direct bilirubin. Results. Survival (mean +/- SD) of the anhepatic pigs was significantly increased in the BAL-treated group (group III: 65+/-15 hr), as compared with the control groups (group I: 46+/-6 hr and group II: 43+/-14 hr). Mean blood ammonia levels during BAL treatment were significantly lower in the BAL-treated group in comparison with both control groups (P=0.02). Total and direct bilirubin levels gradually increased after hepatectomy and reached maximum values of 1.98 mg/dl and 1.50 mg/dl, respectively, showing no differences between the three groups. Conclusions. (1) Treatment of anhepatic pigs with the AMC-BAL containing autologous hepatocytes significantly increases survival time, which is associated with a significant decrease in blood ammonia. 2) Anhepatic pigs demonstrate increasing direct bilirubin levels as a result of extrahepatic bilirubin conjugation.
引用
收藏
页码:204 / 209
页数:6
相关论文
共 40 条
[1]   Acute liver failure; clinical features and management [J].
Bernal, W ;
Wendon, J .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1999, 11 (09) :977-984
[2]   Enhancement of intestinal UDP-glucuronosyltranferase activity in partially hepatectomized rats [J].
Catania, VA ;
Luquita, MG ;
Pozzi, EJS ;
Mottino, AD .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1998, 1380 (03) :345-353
[3]  
DIXIT V, 1988, EUR J SURG S, P71
[4]   HETEROLOGOUS LIVER PERFUSION IN TREATMENT OF HEPATIC FAILURE [J].
EISEMAN, B ;
LIEM, DS ;
RAFFUCCI, F .
ANNALS OF SURGERY, 1965, 162 (03) :329-&
[5]   A new technique for total hepatectomy in the pig for testing liver support devices [J].
Filipponi, F ;
Boggi, U ;
Meacci, L ;
Burchielli, S ;
Vistoli, F ;
Bellini, R ;
Prota, C ;
Colizzi, L ;
Kusmic, C ;
Campani, D ;
Gneri, C ;
Trivella, MG ;
Mosca, F .
SURGERY, 1999, 125 (04) :448-455
[6]   In vitro evaluation of a novel bioreactor based on an integral oxygenator and a spirally wound nonwoven polyester matrix for hepatocyte culture as small aggregates [J].
Flendrig, LM ;
laSoe, JW ;
Jorning, GGA ;
Steenbeek, A ;
Karlsen, OT ;
Bovee, WMMJ ;
Ladiges, NCJJ ;
teVelde, AA ;
Chamuleau, RAFM .
JOURNAL OF HEPATOLOGY, 1997, 26 (06) :1379-1392
[7]   Significantly improved survival time in pigs with complete liver ischemia treated with a novel bioartificial liver [J].
Flendrig, LM ;
Calise, F ;
Di Florio, E ;
Mancini, A ;
Ceriello, A ;
Santaniello, W ;
Mezza, E ;
Sicoli, F ;
Belleza, G ;
Bracco, A ;
Cozzolino, S ;
Scala, D ;
Mazzone, M ;
Fattore, M ;
Gonzales, E ;
Chamuleau, RAFM .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1999, 22 (10) :701-709
[8]   Evaluation of a novel bioartificial liver in rats with complete liver ischemia:: treatment efficacy and species-specific α-GST detection to monitor hepatocyte viability [J].
Flendrig, LM ;
Chamuleau, RAFM ;
Maas, MAW ;
Daalhuisen, J ;
Hasset, B ;
Kilty, CG ;
Doyle, S ;
Ladiges, NCJJ ;
Jörning, GGA ;
la Soe, JW ;
Sommeijer, D ;
te Velde, AA .
JOURNAL OF HEPATOLOGY, 1999, 30 (02) :311-320
[9]   HYBRID LIVER SUPPORT SYSTEM IN A SHORT-TERM APPLICATION ON HEPATECTOMIZED PIGS [J].
GERLACH, J ;
TROST, T ;
RYAN, CJ ;
MEISSLER, M ;
HOLE, O ;
MULLER, C ;
NEUHAUS, P .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1994, 17 (10) :549-553
[10]   BIOREACTOR FOR A LARGER SCALE HEPATOCYTE IN-VITRO PERFUSION [J].
GERLACH, JC ;
ENCKE, J ;
HOLE, O ;
MULLER, C ;
RYAN, CJ ;
NEUHAUS, P .
TRANSPLANTATION, 1994, 58 (09) :984-988