Journal
JOURNAL OF PHARMACY AND PHARMACOLOGY
Volume 53, Issue 6, Pages 867-872Publisher
WILEY
DOI: 10.1211/0022357011776027
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The anti-inflammatory activity of abietic acid, a diterpene isolated from Pimenta racemosa var. grissea (Myrtaceae), was evaluated in-vivo and in-vitro. This compound significantly inhibited rat paw oedema induced by carrageenan in a time- and dose-dependent manner, and mouse ear oedema induced by 12-O-tetradecanoylphorbol acetate, after oral or topical administration. The inhibition of myeloperoxidase enzyme showed that its topical activity was influenced by neutrophil infiltration into the inflamed tissues (ears). In addition, the effect of abietic acid on some macrophage functions was analysed in-vitro. Non-toxic concentrations of abietic acid inhibited prostaglandin E-2 (PGE(2)) production in lipopolysaccharide-treated macrophages, whereas nitrite, tumour necrosis factor alpha and interleukin-1 beta production were only weakly affected by this diterpene. PGE(2) production from A23187-stimulated macrophages was only inhibited at high doses (100 muM) and it failed to modify leukotriene C-4 production. These results indicate that abietic acid exerts in-vivo anti-inflammatory activity after oral or topical administration and has partial ability to prevent the production of some inflammatory mediators.
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