Fatty liver and anti-oxidant enzyme activities along with peroxisome proliferator-activated receptors γ and α expressions in the liver of Wilson's disease

Mol Genet Metab. 2012 Nov;107(3):542-7. doi: 10.1016/j.ymgme.2012.08.004. Epub 2012 Aug 11.

Abstract

Background: The mechanisms of liver damage and steatosis in Wilson's disease (WD) presenting accumulation of copper generating oxidants remain unclear. Recent studies have shown that peroxisome proliferator-activated receptors (PPARs), in particular PPARs α and γ, regulate fat content of the liver together with the anti-oxidant and anti-inflammation systems. However, such PPARs have never been studied in WD.

Methods: We examined PPARs along with the liver damage and steatosis of WD using liver specimens from affected patients exhibiting mild liver damage (group I, n = 5), moderate or greater liver damage (group II, n = 10) and fulminant hepatic failure (group III, n = 5), and from asymptomatic carriers (group H, n = 4).

Results: PPAR α expression was increased over the control levels in groups H and I but was decreased in groups II and III in parallel with the progression of liver damage (group H = I>II>III). PPAR γ expression was inversely increased (group H<I<II<III). Mn-dependent superoxide dismutase (Mn-SOD), CuZn-SOD, and catalase activities were decreased in the affected three groups, and were increased in group H. Among group II exhibiting substantial inter-individual variances in parameters, the severity of steatosis showed a significant positive correlation with PPAR γ expression (p<0.001) but not PPAR α expression. CuZn-SOD activity was positively correlated with PPARα expression (p<0.05) but not PPAR γ expression.

Conclusion: These results suggest that changes of PPARs γ and α are associated with the steatosis and the impairment of anti-oxidant system in the liver of WD.

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adolescent
  • Adult
  • Asymptomatic Diseases
  • Catalase / metabolism*
  • Cation Transport Proteins / genetics
  • Child
  • Child, Preschool
  • Copper / metabolism
  • Copper-Transporting ATPases
  • Fatty Liver / genetics*
  • Fatty Liver / metabolism
  • Fatty Liver / pathology
  • Female
  • Gene Expression
  • Hepatolenticular Degeneration / genetics*
  • Hepatolenticular Degeneration / metabolism
  • Hepatolenticular Degeneration / pathology
  • Humans
  • Isoenzymes / metabolism
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Mutation
  • PPAR alpha / genetics*
  • PPAR alpha / metabolism
  • PPAR gamma / genetics*
  • PPAR gamma / metabolism
  • Severity of Illness Index
  • Superoxide Dismutase / metabolism*

Substances

  • Cation Transport Proteins
  • Isoenzymes
  • PPAR alpha
  • PPAR gamma
  • Copper
  • Catalase
  • Superoxide Dismutase
  • Adenosine Triphosphatases
  • Copper-Transporting ATPases