Anti-apoptotic and hepatoprotective effects of gomisin A on fulminant hepatic failure induced by D-galactosamine and lipopolysaccharide in mice

J Pharmacol Sci. 2008 Feb;106(2):225-33. doi: 10.1254/jphs.fp0071738. Epub 2008 Feb 9.

Abstract

This study examined the effects of gomisin A, a lignan compound from Schisandra fructus, on D-galactosamine (GalN) and lipopolysaccharide (LPS)-induced hepatic apoptosis and liver failure. Mice were given an intraperitoneal injection of GalN (700 mg/kg) / LPS (10 microg/kg). Gomisin A (25, 50, 100, and 200 mg/kg) was administered intraperitoneally 1 h before the GalN/LPS injection. The liver injury was assessed biochemically and histologically. GalN/LPS increased the serum aminotransferase levels and lipid peroxidation but decreased the reduced glutathione level. The pretreatment with gomisin A attenuated these changes in a dose-dependent manner. The survival rate of the gomisin A group was significantly higher than that of the control. The mitochondria isolated after the mice had been injected with GalN/LPS were swollen, which was attenuated by the gomisin A pretreatment. The elevation of serum tumor necrosis factor-alpha and activation of caspase-3 were observed in the GalN/LPS group, which was attenuated by gomisin A. The gomisin A-pretreated groups showed significantly fewer apoptotic (TUNEL-positive) cells and DNA fragmentation as compared with the GalN/LPS mice. The liver protection afforded by gomisin A is the result of the reduced oxidative stress and its anti-apoptotic activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Apoptosis
  • Caspase 3 / blood
  • Cyclooctanes / therapeutic use*
  • DNA Fragmentation
  • Dioxoles / therapeutic use*
  • Galactosamine
  • Glutathione / metabolism
  • Lignans / therapeutic use*
  • Lipid Peroxidation / drug effects
  • Lipopolysaccharides
  • Liver Failure / chemically induced
  • Liver Failure / metabolism
  • Liver Failure / pathology
  • Liver Failure / prevention & control*
  • Male
  • Mice
  • Mice, Inbred ICR
  • Mitochondria, Liver / drug effects
  • Mitochondria, Liver / metabolism
  • Mitochondrial Swelling / drug effects
  • Oxidative Stress / drug effects
  • Protective Agents / therapeutic use*
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Cyclooctanes
  • Dioxoles
  • Lignans
  • Lipopolysaccharides
  • Protective Agents
  • Tumor Necrosis Factor-alpha
  • schizandrol B
  • Galactosamine
  • Alanine Transaminase
  • Caspase 3
  • Glutathione