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Purification and characterization of the biological effects of phospholipase A(2) from sea anemone Bunodosoma caissarum

dc.contributor.authorMartins, Rene D.
dc.contributor.authorAlves, Renata S.
dc.contributor.authorMartins, Alice M. C.
dc.contributor.authorBarbosa, Paulo Sergio F.
dc.contributor.authorEvangelista, Janaina S. A. M.
dc.contributor.authorEvangelista, João José F.
dc.contributor.authorXimenes, Rafael M.
dc.contributor.authorToyama, Marcos H. [UNESP]
dc.contributor.authorToyama, Daniela O.
dc.contributor.authorSouza, Alex Jardelino F.
dc.contributor.authorOrts, Diego J. B. [UNESP]
dc.contributor.authorMarangoni, Sergio
dc.contributor.authorMenezes, Dalgimar B. de
dc.contributor.authorFonteles, Manasses C.
dc.contributor.authorMonteiro, Helena S. A.
dc.contributor.institutionUniversidade Federal do Ceará (UFC)
dc.contributor.institutionUniversidade Estadual do Ceará (UECE)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Prebiteriana Mackenzie
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2014-05-20T13:12:20Z
dc.date.available2014-05-20T13:12:20Z
dc.date.issued2009-09-15
dc.description.abstractSea anemones contain a variety of biologically active substances. Bunodosoma caissarum is a sea anemone from the Cnidaria phylum, found only in Brazilian coastal waters. The aim of the present work was to study the biological effects of PLA(2) isolated from the sea anemone B. caissarum on the isolated perfused kidney, the arteriolar mesenteric bed and on insulin secretion. Specimens of B. caissarum were collected from the Sao Vicente Channel on the southern coast of the State of São Paulo, Brazil. Reverse phase HPLC analysis of the crude extract of B. caissarum detected three PLA(2) proteins (named BcPLA(2)1, BCPLA(2)2 and BcPLA(2)3) found to be active in B. caissarum extracts. MALDI-TOF mass spectrometry of BcPLA(2)1 showed one main peak at 14.7 kDa. The N-terminal amino acid sequence of BcPLA(2)1 showed high amino acid sequence identity with PLA(2) group III protein isolated from the Mexican lizard (PA23 HELSU, HELSU, PA22 HELSU) and with the honey bee Apis mellifera (PLA(2) and 1POC_A). In addition, BcPLA(2)1 also showed significant overall homology to bee PLA(2). The enzymatic activity induced by native BCPLA(2)1 (20 mu g/well) was reduced by chemical treatment with p-bromophenacyl bromide (p-BPB) and with morin. BcPLA(2)1 strongly induced insulin secretion in presence of high glucose concentration. In isolated kidney, the PLA(2) from B. caissarum increased the perfusion pressure, renal vascular resistance, urinary flow, glomerular filtration rate, and sodium, potassium and chloride levels of excretion. BcPLA(2)1, however, did not increase the perfusion pressure on the mesenteric vascular bed. In conclusion, PLA(2), a group III phospholipase isolated from the sea anemone B. caissarum, exerted effects on renal function and induced insulin secretion in conditions of high glucose concentration. (C) 2009 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUniversidade Federal do Ceará (UFC), Dept Fisiol & Farmacol, Fac Med, Inst Biomed, BR-60420970 Fortaleza, Ceara, Brazil
dc.description.affiliationUniversidade Federal do Ceará (UFC), Clin Res Unit, BR-60420970 Fortaleza, Ceara, Brazil
dc.description.affiliationUniversidade Federal do Ceará (UFC), Dept Clin & Toxicol Anal, BR-60420970 Fortaleza, Ceara, Brazil
dc.description.affiliationUniv Estadual Ceara, Fac Vet, Fortaleza, Ceara, Brazil
dc.description.affiliationUniv Estadual Paulista, UNESP, Sao Vicente Unit, São Paulo, Brazil
dc.description.affiliationUniv Prebiteriana Mackenzie, São Paulo, Brazil
dc.description.affiliationUniv Estadual Campinas, Dept Biochem, IB, São Paulo, Brazil
dc.description.affiliationUniversidade Federal do Ceará (UFC), Dept Pathol, BR-60420970 Fortaleza, Ceara, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Sao Vicente Unit, São Paulo, Brazil
dc.format.extent413-420
dc.identifierhttp://dx.doi.org/10.1016/j.toxicon.2009.05.005
dc.identifier.citationToxicon. Oxford: Pergamon-Elsevier B.V. Ltd, v. 54, n. 4, p. 413-420, 2009.
dc.identifier.doi10.1016/j.toxicon.2009.05.005
dc.identifier.issn0041-0101
dc.identifier.urihttp://hdl.handle.net/11449/317
dc.identifier.wosWOS:000268863100005
dc.language.isoeng
dc.publisherPergamon-Elsevier B.V. Ltd
dc.relation.ispartofToxicon
dc.relation.ispartofjcr2.352
dc.relation.ispartofsjr0,692
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectBunodosoma caissarumen
dc.subjectPhospholipase A(2)en
dc.subjectBiological effectsen
dc.titlePurification and characterization of the biological effects of phospholipase A(2) from sea anemone Bunodosoma caissarumen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderPergamon-Elsevier B.V. Ltd
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, São Vicentept
unesp.departmentCiências Biológicas - IBCLPpt

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