Tumor necrosis factor-α affects blood-brain barrier permeability in acetaminophen-induced acute liver failure

Eur J Gastroenterol Hepatol. 2011 Jul;23(7):552-8. doi: 10.1097/MEG.0b013e3283470212.

Abstract

Objectives: Cerebral edema is a major cause of death during acute liver failure (ALF), but the exact mechanism of this condition is still not entirely clear. The aim of this study was to investigate the role of tumor necrosis factor α (TNFα) in changing the permeability of the blood-brain barrier (BBB) during acetaminophen (APAP)-induced ALF.

Materials and methods: ALF animal models were generated by administering APAP. Anti-TNFα-IgG was intravenously injected (100 μg/mouse) 2 h after administration of APAP. We investigated BBB permeability with Evans blue staining, and structure with electron microscopy.

Results: BBB permeability increased in APAP-induced ALF mice and correlated with elevated serum TNFα levels. Electron microscopy of mouse brain tissues revealed tight junction (TJ) disruptions and endothelial cell shrinkage, as well as increased vesicles and vacuoles. In addition, the expression of the TJ-associated protein, occludin, was significantly decreased in APAP-induced ALF mice. Changes in BBB permeability and occludin expression could be prevented by administering anti-TNFα-IgG 2 h after APAP challenge.

Conclusion: TNFα plays a critical role in the development of brain edema in APAP-induced ALF. Increased BBB permeability may be due to the loss of the TJ-associated protein occludin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaminophen / adverse effects*
  • Analgesics, Non-Narcotic / adverse effects*
  • Animals
  • Antibodies, Neutralizing / therapeutic use
  • Blood-Brain Barrier / drug effects
  • Blood-Brain Barrier / pathology
  • Blood-Brain Barrier / physiopathology*
  • Blood-Brain Barrier / ultrastructure
  • Brain Edema / chemically induced
  • Brain Edema / pathology
  • Capillary Permeability*
  • Liver Failure, Acute / chemically induced*
  • Liver Failure, Acute / pathology
  • Male
  • Membrane Proteins / biosynthesis
  • Mice
  • Mice, Inbred BALB C
  • Occludin
  • Tight Junctions / drug effects
  • Tight Junctions / pathology
  • Tight Junctions / ultrastructure
  • Tumor Necrosis Factor-alpha / blood
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / physiology*

Substances

  • Analgesics, Non-Narcotic
  • Antibodies, Neutralizing
  • Membrane Proteins
  • Occludin
  • Ocln protein, mouse
  • Tumor Necrosis Factor-alpha
  • Acetaminophen