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Galactosamine-induced fulminant liver failure--observation in a porcine model.

Abstract
Fulminant hepatic failure can only be treated successfully by liver transplantation, which, however, is not always available. To "bridge" the patient with fulminant hepatic failure until a liver graft is available, various forms of liver support devices had been designed but they were not uniformly successful. To prove the efficacy of a liver support device for fulminant hepatic failure, testing in an animal model is necessary. We attempted to induce a pig model with fulminant hepatic failure by administering galactosamine into pigs and reported the observation. Three pigs were given a dose of 0.5 gm/kg of galactosamine and five pigs were given 1 gm/kg of galactosamine. One pig receiving 0.5 gm/kg galactosamine survived after manifestation of liver failure, while all the other pigs died. The two pigs receiving 0.5 gm/kg galactosamine survived longer than the five pigs receiving 1 gm/kg galactosamine. Before death, a significant elevation of parenchymal liver enzymes, lactate dehydrogenase, bilirubin, bile acid, ammonia, tumour necrosis factor-alpha, activated clotting time, a decrease of platelet concentration, ketone bodies ratio, blood glucose and plasma albumin, and serious impairment of indocyanine green clearance were indicated. At post-mortem, severe liver necrosis was observed. The model may be suitable for testing the efficacy of liver support device for fulminant hepatic failure, preferably 24-48 hours after administration of galactosamine.
AuthorsDavid W Y Ho, Douglas K Lam, Ying-Bo Chen, Jensen To, Irene O L Ng, S T Fan
JournalAsian journal of surgery (Asian J Surg) Vol. 25 Issue 1 Pg. 73-9; discussion 80-1 (Jan 2002) ISSN: 1015-9584 [Print] China
PMID17585450 (Publication Type: Journal Article)
Chemical References
  • Galactosamine
Topics
  • Animals
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Drug Costs
  • Galactosamine (administration & dosage, economics)
  • Liver Failure, Acute (chemically induced, metabolism, pathology)
  • Swine

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