Pathophysiological role of the acute inflammatory response during acetaminophen hepatotoxicity

Cathleen Cover, Jie Liu, Anwar Farhood, Ernst Malle, Michael P. Waalkes, Mary Lynn Bajt, Hartmut Jaeschke

Research output: Contribution to journalArticle

111 Citations (Scopus)

Abstract

Neutrophils are recruited into the liver after acetaminophen (AAP) overdose but the pathophysiological relevance of this acute inflammatory response remains unclear. To address this question, we compared the time course of liver injury, hepatic neutrophil accumulation and inflammatory gene mRNA expression for up to 24 h after treatment with 300 mg/kg AAP in C3Heb/FeJ and C57BL/6 mice. Although there was no relevant difference in liver injury (assessed by the increase of plasma alanine aminotransferase activities and the areas of necrosis), the number of neutrophils and the expression of several pro-inflammatory genes (e.g., tumor necrosis factor-α, interleukin-1β and macrophage inflammatory protein-2) was higher in C3Heb/FeJ than in C57BL/6 mice. In contrast, the expression of the anti-inflammatory genes interleukin-10 and heme oxygenase-1 was higher in C57BL/6 mice. Despite substantial hepatic neutrophil accumulation, none of the liver sections from both strains stained positive for hypochlorite-modified proteins, a specific marker for a neutrophil-induced oxidant stress. In addition, treatment with the NADPH oxidase inhibitors diphenyleneiodonium chloride or apocynin or the anti-neutrophil antibody Gr-1 did not protect against AAP hepatotoxicity. Furthermore, although intercellular adhesion molecule-1 (ICAM-1) was previously shown to be important for neutrophil extravasation and tissue injury in several models, ICAM-1-deficient mice were not protected against AAP-mediated liver injury. Together, these data do not support the hypothesis that neutrophils aggravate liver injury induced by AAP overdose.

Original languageEnglish (US)
Pages (from-to)98-107
Number of pages10
JournalToxicology and Applied Pharmacology
Volume216
Issue number1
DOIs
StatePublished - Oct 1 2006

Fingerprint

Acetaminophen
Liver
Neutrophils
Genes
Inbred C57BL Mouse
Intercellular Adhesion Molecule-1
Wounds and Injuries
Chemokine CXCL2
Hypochlorous Acid
Heme Oxygenase-1
NADPH Oxidase
Alanine Transaminase
Interleukin-1
Oxidants
Interleukin-10
Anti-Inflammatory Agents
Tumor Necrosis Factor-alpha
Tissue
Plasmas
Anti-Idiotypic Antibodies

Keywords

  • Cytokines
  • Hypochlorite
  • Inflammation
  • NAPDH oxidase
  • Neutrophils
  • Oxidant stress

ASJC Scopus subject areas

  • Pharmacology
  • Toxicology

Cite this

Pathophysiological role of the acute inflammatory response during acetaminophen hepatotoxicity. / Cover, Cathleen; Liu, Jie; Farhood, Anwar; Malle, Ernst; Waalkes, Michael P.; Bajt, Mary Lynn; Jaeschke, Hartmut.

In: Toxicology and Applied Pharmacology, Vol. 216, No. 1, 01.10.2006, p. 98-107.

Research output: Contribution to journalArticle

Cover, Cathleen ; Liu, Jie ; Farhood, Anwar ; Malle, Ernst ; Waalkes, Michael P. ; Bajt, Mary Lynn ; Jaeschke, Hartmut. / Pathophysiological role of the acute inflammatory response during acetaminophen hepatotoxicity. In: Toxicology and Applied Pharmacology. 2006 ; Vol. 216, No. 1. pp. 98-107.
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