Ma. Gomez et al., Study of the topical anti-inflammatory activity of Achillea ageratum on chronic and acute inflammation models, Z NATURFO C, 54(11), 1999, pp. 937-941
Citations number
17
Categorie Soggetti
Biochemistry & Biophysics
Journal title
ZEITSCHRIFT FUR NATURFORSCHUNG C-A JOURNAL OF BIOSCIENCES
We have produced a chloroform extract from Achillea which includes stigmast
erol and sitosterol. By comparing it with the pure compounds an anti-inflam
matory effect (with mouse ears) is assumed.
The topical anti-inflammatory effect of the chloroform extract from Achille
a ageratum (Asteraceae)and of stigmasterol and beta-sitosterol, isolated of
this extract has been evaluated, against to 12-0-tetradecanoylphorbol acet
ate (TPA)-induced mouse ear edema, using simple (acute model) and multiple
applications (chronic model) of the phlogistic agent. Myeloperoxydase activ
ity also was studied in the inflamed ears.
In thr acute model the extract exerted a dose-dependent effect. All the dos
es assayed (1, 3 and 5 mg/ear) significantly reduced the edema (50%, 66% an
d 82%, respectively). The isolated sterols stigmasterol and beta-sitosterol
(with doses of 0.5 mg/ear) had similar effect as the extract with doses of
1 and 3 mg (59% and 65% respectively).
In the chronic model the anti-inflammatory effect generally was a more mode
rate one. nit: highest dose of the extract decreased the edema reduction to
26% with the highest dose of the extract applied. With the compounds the e
ffect decreased to 36% with stigmasterol, and 40.6% with beta-sitosterol.
Myeloperoxydase activity (MPO) was reduced by the extract and the compounds
in the acute model, however, in the chronic edema, the enzyme inhibition w
as very weak with all treatments even with the standard substance.
These results indicate that the chloroform extract of Achillea ageratum and
some of the its components stigmasterol and beta-sitosterol are more effec
tive as topical anti-inflammatory agents in acute than in the chronic proce
ss and their action is markedly influenced by the inhibition of neutrophil
migration into inflamed tissue.