Why the study?
Does a high-fat diet induce nonalcoholic steatohepatitis and MARCO expression in wild-type and hyperlipidaemic mice?
Does a high-fat diet induce nonalcoholic steatohepatitis and MARCO expression in wild-type and hyperlipidaemic mice?
Long-term high-fat diet induces NASH and liver-restricted MARCO expression in mice, suggesting endotoxin involvement in NASH pathogenesis, whereas hyperlipidaemia alone is insufficient.
High-fat diet but not hyperlipidaemia alone induces NASH features in mice; leaves open MARCO's role in human pathogenesis.
Nonalcoholic steatohepatitis (NASH) is one of the life-threatening hepatic diseases; however, its pathogenesis is still unknown. To evaluate the causative role of hyperlipidaemia and high-fat diet, we compared C57BL/6 mice with inherited hyperlipidaemic model mice (LDLR(-/-)mice and ApoE(-/-) mice) fed a normal or a high-fat diet. LDLR(-/-) and ApoE(-/-) mice fed the normal diet showed significantly higher serum cholesterol level than that of C57BL/6 mice fed the high-fat diet. These mice, however, have shown neither significant elevation of serum alanine transaminase (ALT) level nor histopathologic features of steatohepatitis. High-fat diet groups of all three strains showed histopathological characteristics of steatohepatitis with elevated serum ALT levels and high expression of macrophage scavenger receptor MARCO mRNA in the liver. Semiquantitative endotoxin analysis showed an elevated serum endotoxin level in the portal vein but not in the vena cava in ApoE(-/-) mice fed the high-fat diet. These results indicate that long-term feeding of a high-fat diet induces NASH, whereas hyperlipidaemia alone is not enough to induce NASH. Liver-restricted induction of MARCO in mice with high-fat diet and portal endotoxaemia in ApoE(-/-) mice fed the high-fat diet suggest the possible involvement of endotoxin in the pathogenesis of NASH.
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Yoshimatsu et al. (2004) studied this question.
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