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.
Key words
Artemisia annua
- Asteraceae - antiulcer activity - sesquiterpenes
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