Differential protection with inhibitors of caspase-8 and caspase-3 in murine models of tumor necrosis factor and Fas receptor-mediated hepatocellular apoptosis

Toxicol Appl Pharmacol. 2001 Sep 15;175(3):243-52. doi: 10.1006/taap.2001.9242.

Abstract

Excessive apoptosis has been implicated in a number of acute and chronic human diseases. The activation of caspases has been shown to be critical for the apoptotic process. The objective of this investigation was to evaluate the beneficial effects and mechanism of action of the caspase-8 inhibitor IETD-CHO and the caspase-3 inhibitor DEVD-CHO against tumor necrosis factor (TNF)-induced hepatocellular apoptosis in vivo and compare these results to effects of the same inhibitors against Fas-induced apoptosis. Treatment of C3Heb/FeJ mice with 700 mg/kg galactosamine/100 microg/kg endotoxin induced parenchymal apoptosis (indicated by caspase-3 activation and morphology) and severe liver injury (indicated by the increase in plasma alanine aminotransferase activities and histology) at 7 h. Treatment with IETD-CHO or DEVD-CHO (10 mg/kg at 3, 4.5, and 5.5 h) significantly attenuated caspase-3 activation and liver injury. Western analysis showed that DEVD-CHO had no effect while IETD-CHO substantially reduced procaspase-3 and procaspase-9 processing. On the other hand, caspase-3 activation and liver injury by the anti-Fas antibody Jo-2 was completely prevented by a single dose of DEVD-CHO and, as previously shown, by IETD-CHO at 90 min. Both inhibitors prevented procaspase-3 and procaspase-9 processing. Thus, there are fundamental differences in the efficacy of caspase inhibitors in these two models. We conclude that Fas may rely exclusively on caspase-8 activation and mitochondria to activate caspase-3, which can process more procaspase-8 and thus propagate the amplification of the apoptotic signal. TNF can activate a similar signaling pathway. However, alternative signaling mechanisms seem to exist, which can compensate if the main pathway is blocked.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Blotting, Western
  • Caspase 3
  • Caspase 8
  • Caspase 9
  • Caspase Inhibitors
  • Cysteine Proteinase Inhibitors / pharmacology*
  • DNA / analysis
  • DNA Fragmentation
  • Galactosamine / pharmacology
  • Hepatocytes / drug effects*
  • Hepatocytes / enzymology
  • Hepatocytes / pathology
  • Liver Failure / chemically induced
  • Liver Failure / pathology
  • Liver Failure / prevention & control*
  • Male
  • Mice
  • Mice, Inbred C3H
  • Models, Animal
  • Oligopeptides / pharmacology*
  • Single-Blind Method
  • Time Factors
  • Tumor Necrosis Factor-alpha / pharmacology
  • fas Receptor / pharmacology

Substances

  • Caspase Inhibitors
  • Cysteine Proteinase Inhibitors
  • Oligopeptides
  • Tumor Necrosis Factor-alpha
  • acetyl-isoleucyl-glutamyl-threonyl-aspartyl-aldehyde
  • aspartyl-glutamyl-valyl-aspartal
  • fas Receptor
  • Galactosamine
  • DNA
  • CASP3 protein, human
  • CASP8 protein, human
  • CASP9 protein, human
  • Casp3 protein, mouse
  • Casp8 protein, mouse
  • Casp9 protein, mouse
  • Caspase 3
  • Caspase 8
  • Caspase 9