The concentration of zileuton used in the present study is able to completely block the synthesis of eicosanoids produced by the lipoxygenase pathway (Horizoe et al., 1998; Canetti et al., 2003). Previous observations on the reversal of the inhibitory action of venom and crotoxin by zileuton (Sampaio

et al., 2006; Nunes et al., 2010), as well as the prevention of the inhibitory effect of venom in edema by zileuton observed in the present study, strongly suggest the involvement of eicosanoids from the lipoxygenase pathway in modulating the inhibitory action of venom. We do not yet have unambiguous data on which component or components generated in the lipoxygenase pathway could be involved in the inhibitory effect of the venom. However, this set of results, in conjunction with data obtained from macrophage culture studies and models of acute inflammatory response

(Sampaio Thiazovivin datasheet et al., 2006; Nunes et al., 2010) suggest the involvement of lipoxins in this process. It is known that Cdt venom is able to induce the generation of lipoxins in cultured macrophages (Sampaio et al., 2006) and that the inhibitory activity of this venom on the acute inflammation induced by carrageenan depends on their action on formyl find more peptide receptors, which are related to lipoxins or resolvins (Nunes et al., 2010). Studies have shown that lipoxins may regulate the chronic and the acute inflammatory responses (Kantarci and van Dyke, 2003). Considering that lipoxins need to bind to G-protein coupled receptors, such as

formyl peptides receptors family, to exert their biological actions (Chiang and Serhan, 2006; Ye et al. 2009), the results obtained in the present study with animals pre-treated with Boc2, a specific inhibitor of formyl peptide receptors, reinforce a possible involvement of lipoxins in this inhibitory effect of the Cdt venom on this chronic inflammatory response. To identify which component in the Cdt venom is responsible for the toxin’s inhibitory effect on chronic edema induced by BCG, we found that crotoxin, the major component of the venom and the main toxin responsible for the observed effects in the pathophysiology of Crotalus Reverse transcriptase envenoming, was the only component that presented similar inhibitory results to those observed with crude venom. This result confirms previous studies showing that this toxin interferes with the biological and metabolic activities of macrophages and is responsible for the inhibition of acute inflammatory processes ( Sampaio et al., 2006; Nunes et al., 2010). In conclusion, our results show that C. durissus terrificus venom, and in particular crotoxin, significantly inhibits the chronic paw edema induced by the injection of BCG in mice and suggest that this inhibition may be due to the generation of anti-inflammatory mediator(s) from the lipoxygenase pathway, possibly by the generation of lipoxins.