
pmid: 16275631
New therapeutic approaches for the treatment of allergic diseases can be aided by the development of agents capable of regulating eosinophilic leukocytes. Here, we evaluated the anti-allergic properties of a crude extract of the Brazilian bromeliaceae Nidularium procerum, focusing on its effects on allergic eosinophilia. By studying allergic pleurisy in actively sensitized C57Bl/6 mice, we observed that pretreatment with N. procerum (2 mg/kg; i.p.) reduced pleural eosinophil influx triggered by allergen challenge. N. procerum was also able to reduce lipid body numbers found within infiltrating eosinophils, indicating that N. procerum in vivo is able to affect both migration and activation of eosinophils. Consistently, pretreatment with N. procerum blocked pleural eosinophil influx triggered by PAF or eotaxin, key mediators of the development of allergic pleural eosinophilia. The effect of N. procerum was not restricted to eosinophils, since N. procerum also inhibited pleural neutrophil and mononuclear cell influx. Of note, N. procerum failed to alter the acute allergic reaction, characterized by mast cell degranulation, oedema, and cysteinyl leukotriene release. N. procerum also had direct effects on murine eosinophils, since it inhibited both PAF- and eotaxin-induced eosinophil chemotaxis on an in vitro chemotactic assay. Therefore, N. procerum may be a promising anti-allergic therapy, inasmuch as it presents potent anti-eosinophil activity.
Bromeliaceae, Chemokine CCL11, Inclusion Bodies, Male, Mice, Inbred C3H, Interleukin-13, Dose-Response Relationship, Drug, Lipid Metabolism, Asthma, Eosinophils, Disease Models, Animal, Mice, Cell Movement, Chemokines, CC, Anti-Allergic Agents, Animals, Female, Inflammation Mediators, Bronchoalveolar Lavage Fluid, Cells, Cultured
Bromeliaceae, Chemokine CCL11, Inclusion Bodies, Male, Mice, Inbred C3H, Interleukin-13, Dose-Response Relationship, Drug, Lipid Metabolism, Asthma, Eosinophils, Disease Models, Animal, Mice, Cell Movement, Chemokines, CC, Anti-Allergic Agents, Animals, Female, Inflammation Mediators, Bronchoalveolar Lavage Fluid, Cells, Cultured
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