The antinociceptive and antiedematogenic effects of essential oils (EO, types I and II) from the leaves of two chemotypes of Lippia alba were studied with mice using the hot plate test, acetic acid-induced writhing, and the formalin test, and with rats using paw edema induced by carrageenan or dextran. The results showed dose-dependent inhibition of writhing with doses of 0.5 and 1 mg/kg, i.p., and 1 and 2 mg/kg, p.o., with chemotypes I and II, respectively. A similar but less intense effect was detected in the formalin test, where the two chemotypes (0.5 and 1 mg/kg, i.p.) predominantly inhibited the 2nd phase of the response, and only the effect of the EO I was reversed by the opioid antagonist, naloxone. Latency time to the thermic stimulus as detected by the hot plate test was increased with I but not with II, at doses higher than 10 mg/kg, p.o. A significant antiedematogenic effect was seen at 2 h with 10 and 50 mg/kg, p.o., of I, in paw edema induced by carr ageenan or dextran. However, in the same dose range, II was more effective against dextran-induced edema, but no effect was seen with the carrageenan model. The essential oils of the two types of L. alba are chemically distinct, with I containing a high content of citral and II a high content of carvone with no citral, which could explain the observed differences in their pharmacological actions.
No takes yet. Share an insight, caveat, or question.
Viana et al. (1998) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: