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      Anti-Inflammatory Activity of Chitooligosaccharides in Vivo

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          Abstract

          All the reports to date on the anti-inflammatory activity of chitooligosaccharides (COS) are mostly based on in vitro methods. In this work, the anti-inflammatory activity of two COS mixtures is characterized in vivo (using balb/c mice), following the carrageenan-induced paw edema method. This is a widely accepted animal model of acute inflammation to evaluate the anti-inflammatory effect of drugs. Our data suggest that COS possess anti-inflammatory activity, which is dependent on dose and, at higher doses, also on the molecular weight. A single dose of 500 mg/kg b.w. weight may be suitable to treat acute inflammation cases; however, further studies are needed to ascertain the effect upon longer inflammation periods as well as studies upon the bioavailability of these compounds.

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          Most cited references15

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          Carrageenin-induced edema in hind paw of the rat as an assay for antiiflammatory drugs.

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            Biphasic development of carrageenin edema in rats.

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              Hyaluronan: a multifunctional, megaDalton, stealth molecule.

              Hyaluronan has been implicated in biological processes such as cell adhesion, migration and proliferation. Traditionally, it was thought to be associated with the extracellular matrix, but, hyaluronan may also have unimagined roles inside the cell. Investigation of hyaluronan synthesis and degradation, the identification of new receptors and binding proteins, and the elucidation of hyaluronan-dependent signaling pathways are providing novel insights into the true biological functions of this fascinating molecule.
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                Author and article information

                Journal
                Mar Drugs
                MD
                Marine Drugs
                Molecular Diversity Preservation International
                1660-3397
                2010
                28 May 2010
                : 8
                : 6
                : 1763-1768
                Affiliations
                [1 ] CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, P-4200-072 Porto, Portugal; E-Mails: mmpintado@ 123456esb.ucp.pt (M.E.P.); fxmalcata@ 123456docente.ismai.pt (F.X.M.)
                [2 ] CPQBA/Divisão de Farmacologia e Toxicologia, Universidade Estadual de Campinas, Campinas, São Paulo, Brazil; E-Mails: hmspindola@ 123456hotmail.com (H.S.); vanahelena@ 123456hotmail.com (V.d.S.); carvalho_je@ 123456yahoo.com.br (J.E.C.)
                [3 ] Serviço de Bioquímica, Faculdade de Farmácia da Universidade do Porto, Rua Aníbal Cunha, P-4050-047 Porto, Portugal; E-Mail: assilva@ 123456ff.up.pt (A.S.-S.)
                [4 ] Instituto de Biologia Molecular e Celular (IBMC) da Universidade do Porto, Rua do Campo Alegre, P-4169-007 Porto, Portugal
                Author notes
                *Author to whom correspondence should be addressed; E-Mail: jfernandes@ 123456email.com ; Tel.: +351-96-7892999; Fax: +351-22-5090351.
                Article
                marinedrugs-08-01763
                10.3390/md8061763
                2901823
                20631868
                88e59a31-a555-4fa4-bb05-9d9ca53feb93
                © 2008 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland

                This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 15 April 2010
                : 14 May 2010
                : 26 May 2010
                Categories
                Communication

                Pharmacology & Pharmaceutical medicine
                animal model,anti-inflammatory,chitooligosaccharides

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