Antiulcerogenic activity of some sesquiterpene lactones isolated from Artemisia annua

Planta Med. 2002 Jun;68(6):515-8. doi: 10.1055/s-2002-32570.

Abstract

Artemisinin 1, dihydro-epideoxyarteannuin B 2 and deoxyartemisinin 3 were isolated from the sequiterpene lactone-enriched fraction obtained from the crude ethanolic extract of Artemisia annua L. These compounds were tested on ethanol and indomethacin-induced ulcer models. Compound 1 did not afford cytoprotection under the experimental models tested. Only compounds 2 and 3 decreased the ulcerative lesion index produced by ethanol and indomethacin in rats. These compounds did not demonstrate antiulcerogenic activity when tested on the ethanol-induced ulcer model, with previous administration of indomethacin, suggesting that the antiulcerogenic activity is a consequence of prostaglandin synthesis increase.

MeSH terms

  • Animals
  • Anti-Ulcer Agents / chemistry
  • Anti-Ulcer Agents / pharmacology*
  • Anti-Ulcer Agents / therapeutic use
  • Artemisinins*
  • Asteraceae*
  • Carbenoxolone / pharmacology
  • Cimetidine / pharmacology
  • Drug Interactions
  • Ethanol / administration & dosage
  • Indomethacin / administration & dosage
  • Male
  • Phytotherapy
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Plant Extracts / therapeutic use
  • Rats
  • Rats, Wistar
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / isolation & purification
  • Sesquiterpenes / pharmacology*
  • Sesquiterpenes / therapeutic use
  • Stomach / drug effects*
  • Stomach / pathology
  • Stomach Ulcer / chemically induced
  • Stomach Ulcer / drug therapy*

Substances

  • Anti-Ulcer Agents
  • Artemisinins
  • Plant Extracts
  • Sesquiterpenes
  • deoxyartemisinin 3
  • Ethanol
  • deoxyartemisinin
  • Cimetidine
  • artemisinin
  • Carbenoxolone
  • Indomethacin