Probiotics and antibodies to TNF inhibit inflammatory activity and improve nonalcoholic fatty liver disease

Hepatology. 2003 Feb;37(2):343-50. doi: 10.1053/jhep.2003.50048.

Abstract

Ob/ob mice, a model for nonalcoholic fatty liver disease (NAFLD), develop intestinal bacterial overgrowth and overexpress tumor necrosis factor alpha (TNF-alpha). In animal models for alcoholic fatty liver disease (AFLD), decontaminating the intestine or inhibiting TNF-alpha improves AFLD. Because AFLD and NAFLD may have a similar pathogenesis, treatment with a probiotic (to modify the intestinal flora) or anti-TNF antibodies (to inhibit TNF-alpha activity) may improve NAFLD in ob/ob mice. To evaluate this hypothesis, 48 ob/ob mice were given either a high-fat diet alone (ob/ob controls) or the same diet + VSL#3 probiotic or anti-TNF antibodies for 4 weeks. Twelve lean littermates fed a high-fat diet served as controls. Treatment with VSL#3 or anti-TNF antibodies improved liver histology, reduced hepatic total fatty acid content, and decreased serum alanine aminotransferase (ALT) levels. These benefits were associated with decreased hepatic expression of TNF-alpha messenger RNA (mRNA) in mice treated with anti-TNF antibodies but not in mice treated with VSL#3. Nevertheless, both treatments reduced activity of Jun N-terminal kinase (JNK), a TNF-regulated kinase that promotes insulin resistance, and decreased the DNA binding activity of nuclear factor kappaB (NF-kappaB), the target of IKKbeta, another TNF-regulated enzyme that causes insulin resistance. Consistent with treatment-related improvements in hepatic insulin resistance, fatty acid beta-oxidation and uncoupling protein (UCP)-2 expression decreased after treatment with VSL#3 or anti-TNF antibodies. In conclusion, these results support the concept that intestinal bacteria induce endogenous signals that play a pathogenic role in hepatic insulin resistance and NAFLD and suggest novel therapies for these common conditions.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antibodies / pharmacology*
  • DNA / metabolism
  • Dietary Fats / administration & dosage
  • Fatty Acids / metabolism
  • Fatty Liver / metabolism
  • Fatty Liver / pathology*
  • Hepatitis / prevention & control*
  • Insulin Resistance / physiology
  • Ion Channels
  • JNK Mitogen-Activated Protein Kinases
  • Liver / metabolism
  • Male
  • Membrane Transport Proteins*
  • Mice
  • Mice, Inbred C57BL / genetics
  • Mitochondrial Proteins*
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • NF-kappa B / metabolism
  • Obesity / genetics
  • Oxidation-Reduction
  • Probiotics / pharmacology*
  • Proteins / metabolism
  • RNA, Messenger / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology*
  • Uncoupling Protein 2

Substances

  • Antibodies
  • Dietary Fats
  • Fatty Acids
  • Ion Channels
  • Membrane Transport Proteins
  • Mitochondrial Proteins
  • NF-kappa B
  • Proteins
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Ucp2 protein, mouse
  • Uncoupling Protein 2
  • DNA
  • Alanine Transaminase
  • JNK Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinases