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Artif Organs ; 31(2): 148-51, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17298404

ABSTRACT

An extracorporeal bioartificial liver (BAL) that could prevent death from hepatic encephalopathy in acute hepatic insufficiency was aimed to develop. A functional human hepatocellular carcinoma cell line (FLC-4) was cultured in a radial-flow bioreactor. The function of the BAL was tested in mini-pigs with acute hepatic failure induced by alpha-amanitin and lipopolysaccharide. When the BAL system was connected with cultured FLC-4 to three pigs with hepatic dysfunction, all demonstrated electroencephalographic improvement and survived. Relatively low plasma concentrations of S-100 beta protein, as a marker of astrocytic damage, from pigs with hepatic failure during BAL therapy were noted. BAL therapy can prevent irreversible brain damage from hepatic encephalopathy in experimental acute hepatic failure.


Subject(s)
Bioreactors , Hepatic Encephalopathy/therapy , Liver, Artificial , Amanitins , Animals , Cells, Cultured , Enzyme-Linked Immunosorbent Assay , Hepatic Encephalopathy/blood , Hepatic Encephalopathy/chemically induced , Lipopolysaccharides , Male , Nerve Growth Factors/blood , S100 Calcium Binding Protein beta Subunit , S100 Proteins/blood , Swine , Swine, Miniature
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