Protective effects of esculentic acid against endotoxic shock in Kunming mice

Int Immunopharmacol. 2014 Nov;23(1):229-35. doi: 10.1016/j.intimp.2014.08.022. Epub 2014 Sep 18.

Abstract

Esculentic acid (EA), a triterpene compound extracted from the root of Phytolacca esculenta (the Chinese name Shang Lu), has been widely used to therapy a variety of inflammatory diseases such as rheumatoid arthritis, edema, hepatitis and bronchitis. The present study was designed to investigate the protective effects of EA against LPS-induced endotoxic shock by the intraperitoneal injection of EA (1, 5 and 10 mg/kg) prior to LPS stimulation (1 mg/kg, i.p.). We examined the effects of EA on the survival rate of mice, inflammatory cytokine and pro-inflammatory mediator production, histopathological changes and protein expression of COX-2 in tissue sections from lung, liver and kidney. The results indicate that EA not only increases the survival rate of mice, but decreases the levels of TNF-α, IL-6, NO and PGE2 in serum or tissues, histopathological changes and COX-2 protein expression also. Furthermore, EA also increases the levels of anti-inflammatory cytokine IL-10 in serum. Overall, these data suggest that the protective effects of EA against LPS-induced endotoxic shock may be mediated, at least in part, by regulation the release of inflammatory cytokines and mediators, and protein expression of COX-2 in mice.

Keywords: Cyclooxygenase-2; Endotoxic shock; Esculentic acid; Inflammatory cytokines; Pro-inflammatory mediators.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism*
  • Cytokines / metabolism
  • Dinoprostone / blood
  • Disease Models, Animal
  • Down-Regulation / drug effects
  • Humans
  • Inflammation Mediators / metabolism
  • Lipopolysaccharides / administration & dosage
  • Male
  • Mice
  • Mice, Inbred Strains
  • Phytolacca / immunology
  • Phytotherapy / methods*
  • Shock, Septic / chemically induced
  • Shock, Septic / drug therapy*
  • Triterpenes / therapeutic use*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cytokines
  • Inflammation Mediators
  • Lipopolysaccharides
  • Triterpenes
  • esculentic acid
  • Cyclooxygenase 2
  • Dinoprostone