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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/130610
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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.-
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.date.accessioned2014-05-20T13:12:24Z-
dc.date.accessioned2016-10-25T21:21:35Z-
dc.date.available2014-05-20T13:12:24Z-
dc.date.available2016-10-25T21:21:35Z-
dc.date.issued2011-01-01-
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.issn1678-9180-
dc.identifier.issn1678-9199-
dc.identifier.urihttp://hdl.handle.net/11449/130610-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/130610-
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.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.language.isoeng-
dc.publisherUniversidade Estadual Paulista (UNESP), Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP)-
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.typeoutro-
dc.contributor.institutionUniversidade Federal do Ceará (UFC)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
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.identifier.doi10.1590/S1678-91992011000300014-
dc.identifier.scieloS1678-91992011000300014-
dc.identifier.wosWOS:000294438900013-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileS1678-91992011000300014-en.pdf-
dc.relation.ispartofJournal of Venomous Animals and Toxins Including Tropical Diseases-
dc.identifier.scopus2-s2.0-80052745540-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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