Peripheral antinociception and anti-edematogenic effect of a sulfated polysaccharide from Acanthophora muscoides |
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Authors: | Ana L.G. Quinderé Bruno R. Fontes Edfranck de S.O. Vanderlei Ismael N.L. de Queiroz José A.G. Rodrigues Ianna W.F. de Araújo Roberta J.B. Jorge Dalgimar B. de Menezes Antonio A.R. e Silva Hellíada V. Chaves Janaina S.A.M. Evangelista Mirna M. Bezerra Norma M.B. Benevides |
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Affiliation: | 1. Department of Biochemistry and Molecular Biology, Federal University of Ceará, Avenida Humberto Monte, s/n, Zip Code: 60455-760, Fortaleza, Brazil;2. Department of Physiology and Pharmacology, Federal University of Ceará, Avenida Coronel Nunes de Melo, 1127, Zip Code: 60430-270, Fortaleza, Brazil;3. Department of Pathology and Forensic Medicine, Federal University of Ceará, Rua Monsenhor Furtado, s/n, Zip Code: 60441-750, Fortaleza, Brazil;4. Faculty of Dentistry, Federal University of Ceará, Rua Comandante Maurocélio Rocha Ponte, 100, Zip Code: 62042-280, Sobral, Brazil;5. Faculty of Veterinary Medicine, State University of Ceará, Avenida Paranjana, 1700, Zip Code: 60740-903, Fortaleza, Brazil;6. Faculty of Medicine, Federal University of Ceará, Rua Comandante Maurocélio Rocha Ponte, 100, Zip Code: 62042-280, Sobral, Brazil |
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Abstract: | BackgroundSulfated polysaccharides from red marine algae have presented a variety of potentially therapeutic biological effects, however, their antinocicpetive and anti-inflammatory properties are not well understood.MethodsMale Swiss mice were pretreated with a sulfated polysaccharidic fraction obtained from the marine alga Acanthophora muscoides (AmII) (1, 3 or 9 mg/kg, iv) 30 min prior to either receiving an injection of 0.8% acetic acid or 1% formalin or prior to a thermal stimulus. AmII (1, 3 or 9 mg/kg, sc) was evaluated on carrageenan-, dextran- bradykinin-, histamine- and serotonin-induced rat paw edema models. AmII (500 jig, sc) was also injected into the paw. Additionally, mice were treated with the total sulfated polysaccharides from A. muscoides (Am-TSP) (20 mg/kg, ip) for 14 days.ResultsAmII reduced the number of acetic acid-induced writhes and licking time in the second phase of the formalin test, but it did not alter the response latency in the hot plate test, suggesting that its antinociceptive action occurs through a peripheral mechanism. AmII did not reduce carrageenan-induced paw edema and MPO activity. However, it reduced dextran-, histamine- and serotonin- induced paw edemas, but not bradykinin-induced edema, suggesting that histamine is the major target of AmII anti-edematogenic activity. AmII inj ected into the paw did not evoke local edema. Furthermore, Am-TSP induced no consistent signs of systemic damage, as revealed by body mass, organs wet weight and by biochemical, hematological and histopathological analyses.ConclusionAmII has important antinociceptive and anti-inflammatory properties and represents an important therapeutic agent warranting future studies. |
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Keywords: | marine alga sulfated polysaccharide nociception inflammation |
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