A surgical model of fulminant hepatic failure in rabbits
Version of Record online: 13 JUN 2007
Volume 27, Issue 10, pages 1333–1341, December 2007
How to Cite
Hung, K.-C., Yong, C.-C., Chen, Y.-S., Eng, H.-L., Kuo, F.-Y., Lin, C.-C., Young, T.-H., Kobayashi, E., Chen, C.-L. and Wang, C.-C. (2007), A surgical model of fulminant hepatic failure in rabbits. Liver International, 27: 1333–1341. doi: 10.1111/j.1478-3231.2007.01512.x
- Issue online: 13 JUN 2007
- Version of Record online: 13 JUN 2007
- Received 22 February 2007accepted 16 March 2007
- animal model;
- hepatic encephalopathy;
- intracranial pressure
Aim: Animal models of fulminant hepatic failure (FHF) have been developed for characterization of disease progression and to evaluate the effectiveness of liver-assist devices, some by treatment with hepatotoxic drugs, viral hepatitis or surgical procedures. We have developed a model in the rabbit by combining resection of the three anterior lobes with ligation of the pedicle of the right lateral lobes, resulting in liver necrosis; the remnant quadrate lobes are left intact.
Materials and methods: Adult male New Zealand white rabbits (n=16) were used. Six animals were killed to measure the weight of the separate liver lobes. The others (n=10) underwent left neck central line placement to monitor continuous blood pressure and collect blood for laboratory analysis, and a burr hole on the right parietal bone to monitor the intracranial pressure (ICP). Blood laboratory analysis, clinical hepatic encephalopathy and ICP levels were measured in FHF animals (n=6). Animals (n=4) undergoing a sham operation served as controls.
Results: All FHF animals died between 12 and 26 h after liver surgery from FHF characterized by a progressive increase in liver enzymes, ammonia, total bilirubin, coagulopathy, hepatic encephalopathy and intracranial hypertension. Histological features of the ischaemic lobes showed coagulative necrosis of hepatocytes with absence of nuclei and collapse of cell plates. Brain histology revealed hypoxic cell damage.
Conclusion: We have developed a simple, reproducible model of FHF in rabbits that has a number of features comparable with clinical FHF patients and is well suited for testing experimental bioartificial liver systems and investigating the pathogenesis of FHF.