The effect of hepatic ischemia reperfusion injury in a murine model of nonalcoholic steatohepatitis

J Surg Res. 2011 Jul;169(1):e7-14. doi: 10.1016/j.jss.2011.01.056. Epub 2011 Mar 2.

Abstract

Background: Nonalcoholic fatty liver disease (NAFLD) refers to an increasingly diagnosed condition involving triglyceride accumulation into hepatocytes resulting in a broad spectrum of liver injury. The progression of NAFLD, a relatively benign condition, to nonalcoholic steatohepatitis (NASH) involves the hepatic infiltration of inflammatory cells and subsequent hepatocellular injury. Ischemia/reperfusion (I/R) injury of the liver is a major complication of liver resection, hepatic trauma, and liver transplantation. To date, there have been no studies that have evaluated the effects of hepatic I/R on models of NASH.

Objective: Evaluate the effects of hepatic I/R on a mouse model of NASH.

Methods: A mouse model of progressive NASH was developed and evaluated using C57BL/6 mice fed a methionine choline deficient diet for 3, 6, 9, and 12 wk. Mice subsequently underwent 90 min of partial hepatic ischemia with reperfusion of 1, 4, and 8 h. Mice were sacrificed after the indicated periods, and blood and liver samples were taken for analysis.

Results: Mice fed the MCD diet showed a rapid induction of hepatic steatosis, inflammation, and fibrosis by 3 wk that persisted over the 12-wk period of diet, as demonstrated by histologic examination, alanine aminotransferase (ALT), and liver content of myeloperoxidase (MPO). The response to I/R in livers with progressive NASH fed MCD diet for 3, 6, 9, and 12 wk showed marked neutrophil recruitment and hepatocyte necrosis.

Conclusion: These data suggest the inflammatory response from I/R is augmented in livers with NASH histopathology compared with normal liver.

MeSH terms

  • Alanine Transaminase / metabolism
  • Animals
  • Diet
  • Disease Models, Animal
  • Disease Progression
  • Fatty Liver / etiology
  • Fatty Liver / metabolism
  • Fatty Liver / physiopathology*
  • Ischemia / metabolism
  • Ischemia / pathology
  • Ischemia / physiopathology*
  • Liver / blood supply*
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Methionine / deficiency
  • Mice
  • Mice, Inbred C57BL
  • Non-alcoholic Fatty Liver Disease
  • Peroxidase / metabolism
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / pathology
  • Reperfusion Injury / physiopathology*

Substances

  • Methionine
  • Peroxidase
  • Alanine Transaminase