Publicação:
Renal and vascular effects of Crotalus durissus cumanensis venom and its crotoxin fraction

dc.contributor.authorPereira, T. P.
dc.contributor.authorBezerra de Menezes, R. R. P. P.
dc.contributor.authorTorres, A. F. C.
dc.contributor.authorBrito, T. S.
dc.contributor.authorBatista-Lima, F. J.
dc.contributor.authorVinhote, J. F. C.
dc.contributor.authorSousa, D. F.
dc.contributor.authorXimenes, R. M.
dc.contributor.authorToyama, M. H. [UNESP]
dc.contributor.authorDiz Filho, E. B. S.
dc.contributor.authorMagalhaes, P. J. C.
dc.contributor.authorMonteiro, H. S. A.
dc.contributor.authorMartins, A. M. C.
dc.contributor.institutionUniversidade Federal do Ceará (UFC)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2014-05-20T13:12:24Z
dc.date.available2014-05-20T13:12:24Z
dc.date.issued2011-01-01
dc.description.abstractIn this study, we evaluated the actions of Crotalus durissus cumanensis venom (CDCmV), and its crotoxin (Crtx) fraction, on renal and vascular functions in Wistar rats. In isolated perfused kidneys, CDCmV (10 mu g/mL) significantly increased the perfusion pressure (PP) from 110.7 +/- 2.4 to 125.3 +/- 2.8 mmHg after 30 minutes. This effect was accompanied by an increased renal vascular resistance (RVR) from 5.4 +/- 0.1 to 6.2 +/- 0.2 mmHg/mL. g(-1). min(-1). We observed decreases in urinary flow (UF) from 0.13 +/- 0.01 to 0.05 +/- 001 mL. g(-1). min(-1) and glomerular filtration rate (GFR) from 0.66 +/- 0.06 to 0.18 +/- 0.02 mL. g(-1). min(-1). Crtx did not change PP or RVR, but diminished GFR (from 0.65 +/- 0.05 to 0.26 +/- 003 mL. g(-1). min(-1)) and UF (from 0.11 +/- 0.008 to 0.09 +/- 0.008 mL. g(-1). min(-1)). Both CDCmV and Crtx reduced the percentage of tubular transport of sodium, chloride and potassium. The cytotoxicity of these substances against MDCK cells was tested by the MTT method: only CDCmV caused a decrease in the cell viability with an IC50 of 5.4 mu g/mL. In endothelium-intact isolated aortic rings, CDCmV (0.1 to 30 mu g/mL) increased the sustained phenylephrine-induced contraction to a value of 130.0 +/- 6.6% of its corresponding control, but showed a relaxant effect in endothelium-denuded preparations. Similar results were observed in aortic rings contracted with potassium (40 mM). Crtx was ineffective in aortic ring assays. Thus, it is reasonable to suggest that the renal effects induced by the CDCmV may be due to its influence on the endothelium's ability to release factors that can alter the contractile behavior of vascular smooth muscle. In conclusion, CDCmV is toxic to kidney cells. It changes parameters of the renal function including the glomerular filtration rate, renal vascular resistance and tubular transport. The actions induced by CDCmV also involve endothelium-dependent vasoactive properties. Their effects may be only partially attributed to Crtx.en
dc.description.affiliationUniversidade Federal do Ceará (UFC), Dept Anal Clin & Toxicol, Fac Farm, BR-60420970 Fortaleza, Ceara, Brazil
dc.description.affiliationUniversidade Federal do Ceará (UFC), Dept Physiol & Pharmacol, BR-60420970 Fortaleza, Ceara, Brazil
dc.description.affiliationUNESP Univ Estadual Paulista, São Paulo State Univ, Sao Vicente, SP, Brazil
dc.description.affiliationUniv Estadual Campinas, Dept Biochem, Campinas, SP, Brazil
dc.description.affiliationUnespUNESP Univ Estadual Paulista, São Paulo State Univ, Sao Vicente, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico (FUNCAP)
dc.format.extent333-347
dc.identifierhttp://dx.doi.org/10.1590/S1678-91992011000300014
dc.identifier.citationJournal of Venomous Animals and Toxins Including Tropical Diseases. Botucatu: Cevap-unesp, v. 17, n. 3, p. 333-347, 2011.
dc.identifier.doi10.1590/S1678-91992011000300014
dc.identifier.fileS1678-91992011000300014-en.pdf
dc.identifier.issn1678-9180
dc.identifier.issn1678-9199
dc.identifier.lattes8573195327542061
dc.identifier.scieloS1678-91992011000300014
dc.identifier.scopus2-s2.0-80052745540
dc.identifier.urihttp://hdl.handle.net/11449/130610
dc.identifier.wosWOS:000294438900013
dc.language.isoeng
dc.publisherUniversidade Estadual Paulista (Unesp), Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP)
dc.relation.ispartofJournal of Venomous Animals and Toxins Including Tropical Diseases
dc.relation.ispartofjcr1.782
dc.relation.ispartofsjr0,573
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectCrotalus durissus cumanensis
dc.subjectCrotoxin
dc.subjectKidney
dc.subjectVascular injuries
dc.subjectCrotoxin
dc.subjectSnake venom
dc.subjectAnimal cell
dc.subjectAnimal experiment
dc.subjectAnimal tissue
dc.subjectCell viability
dc.subjectChloride transport
dc.subjectControlled study
dc.subjectCrotalus durissus cumanensis
dc.subjectCytotoxicity
dc.subjectDog
dc.subjectGlomerulus filtration rate
dc.subjectKidney function
dc.subjectKidney tubule absorption
dc.subjectKidney vascular resistance
dc.subjectMale
dc.subjectNephrotoxicity
dc.subjectNonhuman
dc.subjectPerfusion pressure
dc.subjectPotassium transport
dc.subjectRat
dc.subjectSmooth muscle contractility
dc.subjectSnake
dc.subjectSodium transport
dc.subjectUrine flow rate
dc.subjectVascular ring
dc.subjectVascular smooth muscle
dc.subjectVasodilatation
dc.subjectRattus norvegicus
dc.titleRenal and vascular effects of Crotalus durissus cumanensis venom and its crotoxin fractionen
dc.typeArtigo
dcterms.licensehttp://www.scielo.br/revistas/jvatitd/iaboutj.htm
dcterms.rightsHolderCevap-unesp
dspace.entity.typePublication
unesp.author.lattes8573195327542061
unesp.author.orcid0000-0003-3109-9683[2]
unesp.author.orcid0000-0002-9073-5750[11]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, São Vicentept
unesp.departmentCiências Biológicas - IBCLPpt

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