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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on September 26, 2008; DOI: 10.1124/jpet.108.143792


0022-3565/09/3281-62-68$20.00
JPET 328:62-68, 2009
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TOXICOLOGY

Tumor Necrosis Factor{alpha} Is a Proximal Mediator of Synergistic Hepatotoxicity from Trovafloxacin/Lipopolysaccharide Coexposure

Patrick J. Shaw, Patricia E. Ganey, and Robert A. Roth

Department of Pharmacology and Toxicology, National Food Safety and Toxicology Center, Center for Integrative Toxicology, Michigan State University, East Lansing, Michigan

The use of trovafloxacin (TVX), a fluoroquinolone antibiotic, was severely restricted because of an association of TVX therapy with idiosyncratic hepatotoxicity in patients. The mechanisms underlying idiosyncratic toxicity are unknown; however, one hypothesis is that an inflammatory stress can render an individual sensitive to the drug. Previously, we reported that treatment of mice with TVX and lipopolysaccharide (LPS) induced tumor necrosis factor (TNF) {alpha}-dependent liver injury, whereas TVX or LPS treatment alone was nontoxic. The goal of this study was to elucidate the role of TNF{alpha} in TVX/LPS-induced liver injury. TNF receptor (TNFR) 1 p55-/- and TNFR2 (p75-/-) mice were protected from hepatotoxicity caused by TVX/LPS coexposure, suggesting that TVX/LPS-induced liver injury requires both TNF receptors. TNF{alpha} inhibition using etanercept significantly reduced the TVX/LPS-induced increases in the plasma concentrations of several cytokines around the time of onset of liver injury. However, despite the reduction in chemokines, etanercept treatment did not affect the TVX/LPS-induced hepatic accumulation of neutrophils. In addition, etanercept treatment attenuated TVX/LPS induction of plasminogen activator inhibitor-1, and this was associated with a reduction in hepatic fibrin deposition. Mice treated with TVX and a nontoxic dose of TNF{alpha} also developed liver injury. In summary, TNF{alpha} acts through p55 and p75 receptors to precipitate an innocuous inflammatory cascade. TVX enhances this cascade, converting it into one that results in hepatocellular injury.


Received July 21, 2008; accepted September 25, 2008.

Address correspondence to: Dr. Robert Roth, 221 Food Safety Building, Michigan State University, East Lansing, MI 48824. E-mail: rothr{at}msu.edu




This article has been cited by other articles:


Home page
J. Pharmacol. Exp. Ther.Home page
P. J. Shaw, P. E. Ganey, and R. A. Roth
Trovafloxacin Enhances the Inflammatory Response to a Gram-Negative or a Gram-Positive Bacterial Stimulus, Resulting in Neutrophil-Dependent Liver Injury in Mice
J. Pharmacol. Exp. Ther., July 1, 2009; 330(1): 72 - 78.
[Abstract] [Full Text] [PDF]




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