You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/42348
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSantos, Marcelo L.-
dc.contributor.authorToyama, Daniela O.-
dc.contributor.authorOliveira, Simone C. B.-
dc.contributor.authorCotrim, Camila A.-
dc.contributor.authorDiz-Filho, Eduardo B. S.-
dc.contributor.authorFagundes, Fabio H. R.-
dc.contributor.authorSoares, Veronica C. G.-
dc.contributor.authorAparicio, Ricardo-
dc.contributor.authorToyama, Marcos H.-
dc.date.accessioned2014-05-20T15:33:53Z-
dc.date.accessioned2016-10-25T18:10:32Z-
dc.date.available2014-05-20T15:33:53Z-
dc.date.available2016-10-25T18:10:32Z-
dc.date.issued2011-01-01-
dc.identifierhttp://dx.doi.org/10.3390/molecules16010738-
dc.identifier.citationMolecules. Basel: Mdpi Ag, v. 16, n. 1, p. 738-761, 2011.-
dc.identifier.issn1420-3049-
dc.identifier.urihttp://hdl.handle.net/11449/42348-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/42348-
dc.description.abstractIn this work we have characterized the action of the naringin, a flavonoid found in grapefruit and known for its various pharmacological effects, which include antioxidant, blood lipid lowering and anticancer activity, on the structure and biochemical activities of a secretory phospholipase A (sPLA2) from Crotalus durissus cascavella, an important protein involved in the releasinge of arachidonic acid in phospholipid membranes. sPLA2 was incubated with naringin (mol:mol) at 37 degrees C and a discrete reduction in the UV scanning signal and a modification of the circular dichroism spectra were observed after treatment with naringin, suggesting modifications of the secondary structure of the protein. This flavonoid was able to decrease enzymatic activity and some pharmacological effects, such as myonecrosis, platelet aggregation, and neurotoxic activity caused by sPLA2, however, the inflammatory effect was not affected by naringin. In addition, small angle X-ray scattering (SAXS) data were collected for sPLA2 and naringin-treated sPLA2 to evaluate possible modifications of the protein structure. These structural investigations have shown that sPLA2 is an elongated dimer in solution and after treatment with naringin a conformational change in the dimeric configuration was observed. Our results suggest that structural modification may be correlated with the loss of enzymatic activity and alterations in pharmacological properties.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipFAEPEX/PRP/UNICAMP-
dc.format.extent738-761-
dc.language.isoeng-
dc.publisherMdpi Ag-
dc.sourceWeb of Science-
dc.subjectsecretoy phospholipase A2en
dc.subjectCrotalus durissus cascavellaen
dc.subjectnaringinen
dc.subjectenzymatic activity pharmacological effectsen
dc.subjectsmall angle X-ray scatteringen
dc.titleModulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringinen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniv Presbiteriana Mackenzie-
dc.description.affiliationUNESP CLP, Lab Macromol Quim, São Paulo, Brazil-
dc.description.affiliationUniv Estadual Campinas, Inst Quim, Lab Biol Estrutural & Cristalog, São Paulo, Brazil-
dc.description.affiliationUniv Presbiteriana Mackenzie, CCBS, São Paulo, Brazil-
dc.description.affiliationUniv Estadual Campinas, Inst Biol, Dept Bioquim, São Paulo, Brazil-
dc.description.affiliationUnespUNESP CLP, Lab Macromol Quim, São Paulo, Brazil-
dc.identifier.doi10.3390/molecules16010738-
dc.identifier.wosWOS:000286596400053-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000286596400053.pdf-
dc.relation.ispartofMolecules-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.