Assessment of the AMC-bioartificial liver in the anhepatic pig
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. Pigs (n=15) underwent total hepatectomy with restoration of caval continui...
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Veröffentlicht in: | Transplantation 2002-01, Vol.73 (2), p.204-209 |
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creator | SOSEF, Meindert N ABRAHAMSE, Leo S. L VAN DE KERKHOVE, Maarten-Paul HARTMAN, Robin CHAMULEAU, Rob A. F. M VAN GULIK, Thomas M |
description | 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.
Pigs (n=15) underwent total hepatectomy with restoration of caval continuity using a polyethylene, three-way prosthesis. In group I, 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.
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.
(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. |
doi_str_mv | 10.1097/00007890-200201270-00009 |
format | Article |
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Pigs (n=15) underwent total hepatectomy with restoration of caval continuity using a polyethylene, three-way prosthesis. In group I, 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.
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.
(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.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/00007890-200201270-00009</identifier><identifier>PMID: 11821731</identifier><identifier>CODEN: TRPLAU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott</publisher><subject>Alanine Transaminase - blood ; Ammonia - blood ; Animals ; Bilirubin - blood ; Biological and medical sciences ; Female ; Hepatectomy ; Liver Failure - mortality ; Liver Failure - therapy ; Liver, Artificial ; Liver, biliary tract, pancreas, portal circulation, spleen ; Medical sciences ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the digestive system ; Swine</subject><ispartof>Transplantation, 2002-01, Vol.73 (2), p.204-209</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13452098$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11821731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SOSEF, Meindert N</creatorcontrib><creatorcontrib>ABRAHAMSE, Leo S. L</creatorcontrib><creatorcontrib>VAN DE KERKHOVE, Maarten-Paul</creatorcontrib><creatorcontrib>HARTMAN, Robin</creatorcontrib><creatorcontrib>CHAMULEAU, Rob A. F. M</creatorcontrib><creatorcontrib>VAN GULIK, Thomas M</creatorcontrib><title>Assessment of the AMC-bioartificial liver in the anhepatic pig</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>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.
Pigs (n=15) underwent total hepatectomy with restoration of caval continuity using a polyethylene, three-way prosthesis. In group I, 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.
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.
(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.</description><subject>Alanine Transaminase - blood</subject><subject>Ammonia - blood</subject><subject>Animals</subject><subject>Bilirubin - blood</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Hepatectomy</subject><subject>Liver Failure - mortality</subject><subject>Liver Failure - therapy</subject><subject>Liver, Artificial</subject><subject>Liver, biliary tract, pancreas, portal circulation, spleen</subject><subject>Medical sciences</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the digestive system</subject><subject>Swine</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0EtLAzEQAOAgiq3VvyB70Vt0JsluJhehFF9Q8aLnJU0TG9mXm63gv3fVikfnMszMx8AMYxnCBYLRlzCGJgNcAAhAoYF_tcwem2IuFS-AYJ9NARRylFJP2FFKr6PIpdaHbIJIArXEKbuap-RTqn0zZG3Iho3P5g8Lvoqt7YcYoou2yqr47vssNt9j22x8Z4fosi6-HLODYKvkT3Z5xp5vrp8Wd3z5eHu_mC95JwoauJUKgAQ5cmvhyBiLAi2ZEHIrgyKvtVArh7IwLlhFwVEBThF6F8RYyhk7_9nb9e3b1qehrGNyvqps49ttKjUqMV6k_oVIkkQuxAhPd3C7qv267PpY2_6j_H3NCM52wCZnq9DbxsX056TKBRiSnyjaclI</recordid><startdate>20020127</startdate><enddate>20020127</enddate><creator>SOSEF, Meindert N</creator><creator>ABRAHAMSE, Leo S. L</creator><creator>VAN DE KERKHOVE, Maarten-Paul</creator><creator>HARTMAN, Robin</creator><creator>CHAMULEAU, Rob A. F. M</creator><creator>VAN GULIK, Thomas M</creator><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20020127</creationdate><title>Assessment of the AMC-bioartificial liver in the anhepatic pig</title><author>SOSEF, Meindert N ; ABRAHAMSE, Leo S. L ; VAN DE KERKHOVE, Maarten-Paul ; HARTMAN, Robin ; CHAMULEAU, Rob A. F. M ; VAN GULIK, Thomas M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p268t-a3400828c8cd2c899a121a89ff5a3f48e7724bc1369cfa48fc860c481ecf248f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Alanine Transaminase - blood</topic><topic>Ammonia - blood</topic><topic>Animals</topic><topic>Bilirubin - blood</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Hepatectomy</topic><topic>Liver Failure - mortality</topic><topic>Liver Failure - therapy</topic><topic>Liver, Artificial</topic><topic>Liver, biliary tract, pancreas, portal circulation, spleen</topic><topic>Medical sciences</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the digestive system</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SOSEF, Meindert N</creatorcontrib><creatorcontrib>ABRAHAMSE, Leo S. L</creatorcontrib><creatorcontrib>VAN DE KERKHOVE, Maarten-Paul</creatorcontrib><creatorcontrib>HARTMAN, Robin</creatorcontrib><creatorcontrib>CHAMULEAU, Rob A. F. M</creatorcontrib><creatorcontrib>VAN GULIK, Thomas M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SOSEF, Meindert N</au><au>ABRAHAMSE, Leo S. L</au><au>VAN DE KERKHOVE, Maarten-Paul</au><au>HARTMAN, Robin</au><au>CHAMULEAU, Rob A. F. M</au><au>VAN GULIK, Thomas M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment of the AMC-bioartificial liver in the anhepatic pig</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>2002-01-27</date><risdate>2002</risdate><volume>73</volume><issue>2</issue><spage>204</spage><epage>209</epage><pages>204-209</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><coden>TRPLAU</coden><abstract>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.
Pigs (n=15) underwent total hepatectomy with restoration of caval continuity using a polyethylene, three-way prosthesis. In group I, 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.
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.
(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.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>11821731</pmid><doi>10.1097/00007890-200201270-00009</doi><tpages>6</tpages></addata></record> |
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subjects | Alanine Transaminase - blood Ammonia - blood Animals Bilirubin - blood Biological and medical sciences Female Hepatectomy Liver Failure - mortality Liver Failure - therapy Liver, Artificial Liver, biliary tract, pancreas, portal circulation, spleen Medical sciences Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the digestive system Swine |
title | Assessment of the AMC-bioartificial liver in the anhepatic pig |
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