Influence of histamine in a liver injury model induced by Propionibacterium acnes and lipopolysaccharide

Biol Pharm Bull. 2003 Oct;26(10):1393-7. doi: 10.1248/bpb.26.1393.

Abstract

In normal mice, plasma histamine levels were 29.4+/-10.1 pmol/ml. When 0.1 microg of lipopolysaccharide (LPS) was intravenously injected into Propionibacterium acnes (P. acnes)-primed ICR mice, histamine levels increased remarkably to 61.2+/-15.9 pmol/ml (p<0.001). An increase was also observed in liver tissues. Oral administration of histidine at 200 mg/kg once daily for 5 d before intravenous LPS injection increased the plasma alanine aminotransferase (ALT) activity to 2936.5+/-356.3 IU/l, a significant change compared with the controls (2244.8+/-425.5 IU/l, p<0.05). The 24 h survival rate after LPS injection was 72.7% in the mice treated with 50 mg/kg of ranitidine, in contrast with 50% in the control group although the treatment did not significantly decrease the plasma ALT activity. On the other hand, 50 mg/kg of pyrilamine significantly reduced plasma ALT activity (p<0.001). The results suggested that histamine levels are related to hepatic damage in the P. acnes plus LPS induction of liver injury.

Publication types

  • Comparative Study

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Chemical and Drug Induced Liver Injury
  • Disease Models, Animal*
  • Drug Synergism
  • Histamine / blood*
  • Lipopolysaccharides / toxicity*
  • Liver Diseases / blood*
  • Liver Diseases / microbiology
  • Male
  • Mice
  • Mice, Inbred ICR
  • Propionibacterium acnes*

Substances

  • Lipopolysaccharides
  • Histamine
  • Alanine Transaminase