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Protective effects of E3330, a novel quinone derivative, on galactosamine/tumor necrosis factor-alpha-induced hepatitis in mice.

Abstract
Oral pretreatment with E3330, a novel quinone derivative, attenuated liver injury induced with tumor necrosis factor-alpha in galactosamine-sensitized mice. Tumor necrosis factor-alpha is known to induce inflammatory mediators such as leukotrienes and prostanoids. An in vitro study showed that E3330 inhibited the generation of leukotriene B4 and thromboxane B2, but enhanced prostaglandin E2 generation from rat peritoneal exudate cells stimulated with the Ca(2+)-ionophore, A23187. These findings suggest that the protective effect of E3330 on galactosamine/tumor necrosis factor-alpha hepatitis is due at least in part to its inhibition of the generation of leukotrienes. The inhibition of thromboxane B2 generation or the enhancement of prostaglandin E2 generation by E3330 may also contribute to its hepatoprotective effect.
AuthorsJ Nagakawa, I Hishinuma, K Hirota, K Miyamoto, T Yamanaka, I Yamatsu, K Katayama
JournalEuropean journal of pharmacology (Eur J Pharmacol) Vol. 229 Issue 1 Pg. 63-7 (Dec 08 1992) ISSN: 0014-2999 [Print] Netherlands
PMID1335420 (Publication Type: Journal Article)
Chemical References
  • Benzoquinones
  • Propionates
  • Tumor Necrosis Factor-alpha
  • E 3330
  • Leukotriene B4
  • Thromboxane B2
  • Galactosamine
  • Dinoprostone
Topics
  • Animals
  • Ascitic Fluid (metabolism)
  • Benzoquinones (pharmacology)
  • Chemical and Drug Induced Liver Injury (physiopathology, prevention & control)
  • Dinoprostone (metabolism)
  • Galactosamine
  • In Vitro Techniques
  • Leukotriene B4 (metabolism)
  • Male
  • Mice
  • Mice, Inbred C3H
  • Propionates (pharmacology)
  • Rats
  • Thromboxane B2 (metabolism)
  • Tumor Necrosis Factor-alpha (antagonists & inhibitors, physiology)

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