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Modulation of the Pharmacological Activities of Secretory Phospholipase A2 from Crotalus durissus cascavella Induced by Naringin

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. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniv Presbiteriana Mackenzie
dc.date.accessioned2014-05-20T15:33:53Z
dc.date.available2014-05-20T15:33:53Z
dc.date.issued2011-01-01
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.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.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.identifierhttp://dx.doi.org/10.3390/molecules16010738
dc.identifier.citationMolecules. Basel: Mdpi Ag, v. 16, n. 1, p. 738-761, 2011.
dc.identifier.doi10.3390/molecules16010738
dc.identifier.fileWOS000286596400053.pdf
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/11449/42348
dc.identifier.wosWOS:000286596400053
dc.language.isoeng
dc.publisherMdpi Ag
dc.relation.ispartofMolecules
dc.relation.ispartofjcr3.098
dc.relation.ispartofsjr0,855
dc.rights.accessRightsAcesso aberto
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.typeArtigo
dcterms.licensehttp://www.mdpi.com/about/openaccess
dcterms.rightsHolderMdpi Ag
dspace.entity.typePublication
unesp.author.orcid0000-0002-9176-5767[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, São Vicentept
unesp.departmentCiências Biológicas - IBCLPpt

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