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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/69193
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dc.contributor.authorDos Santos, Michel David-
dc.contributor.authorAlmeida, Maria Camila-
dc.contributor.authorLopes, Norberto Peporine-
dc.contributor.authorDe Souza, Glória Emília Petto-
dc.date.accessioned2014-05-27T11:22:01Z-
dc.date.accessioned2016-10-25T18:22:53Z-
dc.date.available2014-05-27T11:22:01Z-
dc.date.available2016-10-25T18:22:53Z-
dc.date.issued2006-11-01-
dc.identifierhttp://dx.doi.org/10.1248/bpb.29.2236-
dc.identifier.citationBiological and Pharmaceutical Bulletin, v. 29, n. 11, p. 2236-2240, 2006.-
dc.identifier.issn0918-6158-
dc.identifier.issn1347-5215-
dc.identifier.urihttp://hdl.handle.net/11449/69193-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/69193-
dc.description.abstractPhenolic compounds are numerous and ubiquitous in the plant kingdom, being particularly present in health-promoting foods. Epidemiological evidences suggest that the consumption of polyphenol-rich foods reduces the incidence of cancer, coronary heart disease and inflammation. Chlorogenic acid (CGA) is one of the most abundant polyphenol compounds in human diet. Data obtained from in vivo and in vitro experiments show that CGA mostly presents antioxidant and anti-carcinogenic activities. However, the effects of CGA on the inflammatory reaction and on the related pain and fever processes have been explored less so far. Therefore, this study was designed to evaluate the anti-inflammatory, antinociceptive and antipyretic activities of CGA in rats. In comparison to control, CGA at doses 50 and 100 mg/kg inhibited carrageenin-induced paw edema beginning at the 2nd hour of the experimental procedure. Furthermore, at doses 50 and 100 mg/kg CGA also inhibited the number of flinches in the late phase of formalin-induced pain test. Such activities may be derived from the inhibitory action of CGA in the peripheral synthesis/release of inflammatory mediators involved in these responses. On the other hand, even at the highest tested dose (200 mg/kg), CGA did not inhibit the febrile response induced by lipopolysaccharide (LPS) in rats. Additional experiments are necessary in order to clarify the true target for the anti-inflammatory and analgesic effects of CGA. © 2006 Pharmaceutical Society of Japan.en
dc.format.extent2236-2240-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAnalgesic-
dc.subjectAnti-inflammatory-
dc.subjectCarrageenin-
dc.subjectChlorogenic acid-
dc.subjectFormalin-
dc.subjectLipopolysaccharide (LPS)-
dc.subjectchlorogenic acid-
dc.subjectlipopolysaccharide-
dc.subjectpolyphenol derivative-
dc.subjectanalgesic activity-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectantiinflammatory activity-
dc.subjectantineoplastic activity-
dc.subjectantinociception-
dc.subjectantioxidant activity-
dc.subjectantipyretic activity-
dc.subjectcontrolled study-
dc.subjectdose response-
dc.subjectdrug effect-
dc.subjectdrug inhibition-
dc.subjectfever-
dc.subjectinflammation-
dc.subjectmale-
dc.subjectnonhuman-
dc.subjectpain assessment-
dc.subjectpaw edema-
dc.subjectrat-
dc.subjectAdministration, Oral-
dc.subjectAnalgesics-
dc.subjectAnalgesics, Non-Narcotic-
dc.subjectAnimals-
dc.subjectAnti-Inflammatory Agents, Non-Steroidal-
dc.subjectCarrageenan-
dc.subjectChlorogenic Acid-
dc.subjectDisease Models, Animal-
dc.subjectDose-Response Relationship, Drug-
dc.subjectDrug Evaluation, Preclinical-
dc.subjectEdema-
dc.subjectFever-
dc.subjectFlavonoids-
dc.subjectFormaldehyde-
dc.subjectHindlimb-
dc.subjectInflammation-
dc.subjectLipopolysaccharides-
dc.subjectMale-
dc.subjectMolecular Structure-
dc.subjectPain-
dc.subjectPhenols-
dc.subjectRats-
dc.subjectRats, Wistar-
dc.subjectTime Factors-
dc.titleEvaluation of the anti-inflammatory, analgesic and antipyretic activities of the natural polyphenol chlorogenic aciden
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniversity of São Paulo Faculty of Pharmaceutical Sciences of Ribeirão Preto Campus Universitário da USP, Avenida do Café s/n, Ribeirão Preto-SP 14040-903-
dc.description.affiliationUniversity of São Paulo Medical School of Ribeirão Preto Campus Universitário da USP, Avenida dos Bandeirantes 3900, Ribeirão Preto-SP 14049-900-
dc.description.affiliationSão Paulo State University at Rio Claro Department of Zoology, Avenida 24A, 1515, Rio Claro-SP 13506-900-
dc.description.affiliationUnespSão Paulo State University at Rio Claro Department of Zoology, Avenida 24A, 1515, Rio Claro-SP 13506-900-
dc.identifier.doi10.1248/bpb.29.2236-
dc.rights.accessRightsAcesso aberto-
dc.relation.ispartofBiological and Pharmaceutical Bulletin-
dc.identifier.scopus2-s2.0-33750632133-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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