Rosmarinus officinalis L, crude hydroalcoholic (70%) extract was evaluated
for antiulcerogenic activity employing different experimental models. The c
rude hydroalcoholic extract (CHE) decreased the ulcerative lesion index pro
duced by indomethacin, ethanol and reserpine in rats. No antisecretory acti
vity was observed on pyloric ligation model. The previous administration of
L-NAME, a NO-synthase inhibitor, did not reduce the antiulcerogenic activi
ty of CHE in ethanol induced ulcer model, suggesting that the pharmacologic
al mechanism has no relationship with nitric oxide (NO). Whereas when the a
nimal groups were treated with indomethacin, using the same experimental mo
del, CHE did not reduce the antiulcerogenic activity, suggesting that the p
harmacological mechanism has no relationship with prostaglandins. The previ
ous treatment with N-ethymaleimide, a thiol blocker, including mucosal nonp
rotein sulfhydryl groups, reduced the anitulcerogenic activity of CHE on et
hanol induced ulcer model. This result suggests that the crude hydroalcohol
ic extract of R. officinalis L. has active substances that increase the muc
osal nonprotein sulfhydryl groups content. In another hypothesis, the pharm
acological mechanism could be attributed to the activity of antioxidant com
pounds found in the crude hydroalcoholic extract which can react with N-eth
yl-maleimide. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.