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Am J Physiol Gastrointest Liver Physiol 275: G874-G878, 1998;
0193-1857/98 $5.00
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Vol. 275, Issue 5, G874-G878, November 1998

THEMES
Mechanisms of Hepatic Toxicity
III. Intracellular signaling in response to toxic liver injury*

Brett E. Jones and Mark J. Czaja

Department of Medicine and Marion Bessin Liver Research Center, Albert Einstein College of Medicine, Bronx, New York 10461

Toxin-induced liver injury was formerly considered a passive biochemical event, but recent evidence has demonstrated that signal transduction pathways actively modulate the hepatocyte's response to this form of injury. Investigations have examined the effects of a variety of toxins on the activation of receptor-coupled signal transduction, mitogen-activated protein kinases, and Fas signaling, as well as the generation of second messengers such as ceramide and nitric oxide. Many of these pathways culminate in the activation of transcription factors such as activator protein-1, c-Myc, or nuclear factor-kappa B. This Themes article discusses the effects of toxic injury on these signaling pathways and their known functions in regulating hepatocyte death and proliferation following injury.

mitogen-activated protein kinase; ceramide; nitric oxide; activator protein-1; c-Myc; nuclear factor-kappa B; Fas


* Third in a series of invited articles on Mechanisms of Hepatic Toxicity.




This article has been cited by other articles:


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Characterization of Nitric Oxide Production following Isolation of Rat Hepatocytes
Toxicol. Sci., January 1, 2000; 53(1): 56 - 62.
[Abstract] [Full Text] [PDF]




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