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Neo-clerodane diterpenoid, a new metalloprotease snake venom inhibitor from Baccharis trimera (Asteraceae): anti-proteolytic and anti-hemorrhagic properties

dc.contributor.authorJanuario, A. H.
dc.contributor.authorSantos, S. L.
dc.contributor.authorMarcussi, S.
dc.contributor.authorMazzi, IV
dc.contributor.authorPietro, RCLR
dc.contributor.authorSato, D. N.
dc.contributor.authorEllena, J.
dc.contributor.authorSampaio, S. V.
dc.contributor.authorFranca, S. C.
dc.contributor.authorSoares, A. N.
dc.contributor.institutionUniv Ribeirao Preto
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionInstituto Adolfo Lutz (IAL)
dc.date.accessioned2014-05-20T15:26:19Z
dc.date.available2014-05-20T15:26:19Z
dc.date.issued2004-12-07
dc.description.abstractMany plants are used in traditional medicine as active agents against various effects induced by snakebite. Few attempts have been made however to identify the nature of plain natural products with anti-ophidian properties. Baccharis trimera (Less) DC (Asteraceae), known in Brazil as carqueja. has been popularly used to treat liver diseases. rheumatism. diabetes, as well as digestive, hepatic and renal disorders. The active component was identified as 7alpha-hydroxy-3,13-clerodadiene-16,15:18,19-diolide, C20H28O5, (clerodane diterpenoid, Bt-CD). We report now the anti-proteolytic and anti-hemorrhagic propenies against snake venoms of a Bt-CD inhibitor from B. trimera. Bt-CD exhibited full inhibition of hemorrhage and proteolytic activity caused by Bothrops snake venoms. The inhibitor was able to neutralize the hemorrhagic, fibrinogenolytic and caseinolytic activities of class P-I and III metalloproteases isolated from B. neuwiedi and B. jararacussu venoms. No inhibition of the coagulant activity was observed. Bt-CD also partially inhibited the edema induced by other crude venoms, metallopronteases, basic and acidic phospholipases A(2). To further elucidate the inhibitory specificity of Bt-CD against metalloproteases isolated from snake venoms, a deeper understanding of its Structure and function is necessary. Furthermore, the potential use of these inhibitors to complement anti-venom as an alternative treatment of snakebite envenomations needs to be evaluated in future Studies. (C) 2004 Elsevier B.V.. All rights reserved.en
dc.description.affiliationUniv Ribeirao Preto, Unidade Biotecnol, UNAERP, Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv São Paulo, FCFRP, Dept Anal Clin Toxicol & Bromatol, BR-14049 Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv Ribeirao Preto, Curso Ciências Farmaceut, UNAERP, Ribeirao Preto, SP, Brazil
dc.description.affiliationUNESP, Fac Ciências Farmaceut, Ararquara, SP, Brazil
dc.description.affiliationInst Adolfo Lutz Ribeirao Preto, Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv São Paulo, Inst Fis & Quim Sao Carlos, Sao Carlos, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Ciências Farmaceut, Ararquara, SP, Brazil
dc.format.extent243-251
dc.identifierhttp://dx.doi.org/10.1016/j.cbi.2004.09.016
dc.identifier.citationChemico-biological Interactions. Clare: Elsevier Sci Ireland Ltd, v. 150, n. 3, p. 243-251, 2004.
dc.identifier.doi10.1016/j.cbi.2004.09.016
dc.identifier.issn0009-2797
dc.identifier.urihttp://hdl.handle.net/11449/36504
dc.identifier.wosWOS:000225897400004
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofChemico-biological Interactions
dc.relation.ispartofjcr3.296
dc.relation.ispartofsjr1,033
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectBaccharis trimerapt
dc.subjectclerodane diterpenoidpt
dc.subjectsnake venomspt
dc.subjectanti-metalloproteasespt
dc.subjectanti-hemorrhagic activitypt
dc.subjectanti-proteolytic activitypt
dc.subjectanti-ophidian activitypt
dc.titleNeo-clerodane diterpenoid, a new metalloprotease snake venom inhibitor from Baccharis trimera (Asteraceae): anti-proteolytic and anti-hemorrhagic propertiesen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentFármacos e Medicamentos - FCFpt

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