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A rodent model of NASH with cirrhosis, oval cell proliferation and hepatocellular carcinoma.

Authors :
de Lima VM
Oliveira CP
Alves VA
Chammas MC
Oliveira EP
Stefano JT
de Mello ES
Cerri GG
Carrilho FJ
Caldwell SH
Source :
Journal of hepatology [J Hepatol] 2008 Dec; Vol. 49 (6), pp. 1055-61. Date of Electronic Publication: 2008 Sep 24.
Publication Year :
2008

Abstract

Background/aims: Hepatocellular carcinoma (HCC) is a well recognized complication of advanced NASH (non-alcoholic steatohepatitis). We sought to produce a rat model of NASH, cirrhosis and HCC.<br />Methods: Adult Sprague-Dawley rats, weighing 250-300g, were fed a choline-deficient, high trans-fat diet and exposed to DEN in drinking water. After 16 weeks, the animals underwent liver ultrasound (US), sacrifice and assessment by microscopy, immunohistochemistry and transmission electron microscopy (TEM).<br />Results: US revealed steatosis and focal lesions in 6 of 7. All had steatohepatitis defined as inflammation, advanced fibrosis and ballooning with Mallory-Denk bodies (MDB) with frank cirrhosis in 6. Areas of more severe injury were associated with anti-CK19 positive ductular reaction. HCC, present in all, were macro-trabecullar or solid with polyhedral cells with foci of steatosis and ballooned cells. CK19 was positive in single or solid nests of oval cells and in neoplastic hepatocytes. TEM showed ballooning with small droplet fat, dilated endoplasmic reticulum and MDB in non-neoplastic hepatocytes and small droplet steatosis in some cancer cells.<br />Conclusions: This model replicated many features of NASH including steatohepatitis with ballooning, fibrosis, cirrhosis and hepatocellular carcinoma. Oval cell proliferation was evident and the presence anti-CK 19 positivity in the cancer suggests oval cell origin of the malignancy.

Details

Language :
English
ISSN :
0168-8278
Volume :
49
Issue :
6
Database :
MEDLINE
Journal :
Journal of hepatology
Publication Type :
Academic Journal
Accession number :
18929425
Full Text :
https://doi.org/10.1016/j.jhep.2008.07.024