Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1994-5-27
pubmed:abstractText
Metabolic activity of a gel-entrapment, hollow fiber, bioartificial liver was evaluated in vitro and during extracorporeal hemoperfusion in an anhepatic rabbit model. The bioartificial liver contained either 100 million rat hepatocytes (n = 12), fibroblasts (n = 3), or no cells (n = 7) during hemoperfusion of anhepatic rabbits. Eight other anhepatic rabbits were studied without hemoperfusion as anhepatic controls, and three sham rabbits served as normal controls. Albumin production rates (mean +/- SEM) were similar during in vitro (17.0 +/- 2.8 micrograms/h) and extracorporeal (18.0 +/- 4.0 micrograms/h) application of the hepatocyte bioartificial liver. Exogenous glucose requirements were reduced (p < 0.01) and euglycemia was prolonged (p < 0.001) in anhepatic rabbits treated with the hepatocyte bioartificial liver. The maximum rate of glucose production by the hepatocyte bioartificial liver ranged from 50-80 micrograms/h. Plasma concentrations of aromatic amino acids, proline, alanine, and ammonia were normalized in anhepatic rabbits during hepatocyte hemoperfusion. Gel-entrapped hepatocytes in the bioartifical liver performed sulfation and glucuronidation of 4-methylumbelliferone. P450 activity was demonstrated during both in vitro and extracorporeal application of the BAL device by the formation of 3-hydroxy-lidocaine, the major metabolite of lidocaine biotransformation by gel-entrapped rat hepatocytes. In summary, a gel-entrapment, bioartificial liver performed multiple hepatocyte-specific functions without adverse side effects during extracorporeal application in an anhepatic, small animal model. With its potential for short term support of acute liver failure, scale-up of the current bioartificial liver device is indicated for further investigations in large animal, preclinical trials.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0963-6897
pubmed:author
pubmed:issnType
Print
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
441-52
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:8167929-Albumins, pubmed-meshheading:8167929-Amino Acids, pubmed-meshheading:8167929-Animals, pubmed-meshheading:8167929-Artificial Organs, pubmed-meshheading:8167929-Biotransformation, pubmed-meshheading:8167929-Blood Cell Count, pubmed-meshheading:8167929-Blood Glucose, pubmed-meshheading:8167929-Cells, Cultured, pubmed-meshheading:8167929-Collagen, pubmed-meshheading:8167929-Equipment Design, pubmed-meshheading:8167929-Extracorporeal Circulation, pubmed-meshheading:8167929-Gels, pubmed-meshheading:8167929-Hemoperfusion, pubmed-meshheading:8167929-Hepatectomy, pubmed-meshheading:8167929-Hymecromone, pubmed-meshheading:8167929-Lidocaine, pubmed-meshheading:8167929-Liver, pubmed-meshheading:8167929-Male, pubmed-meshheading:8167929-Rabbits, pubmed-meshheading:8167929-Rats, pubmed-meshheading:8167929-Rats, Sprague-Dawley, pubmed-meshheading:8167929-Urea
pubmed:articleTitle
Extracorporeal application of a gel-entrapment, bioartificial liver: demonstration of drug metabolism and other biochemical functions.
pubmed:affiliation
Department of Surgery, University of Minnesota, Minneapolis 55455.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't