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Nephrocalcinosis induced by hyperoxaluria in rats

dc.contributor.authorCunha, Natália Baraldi [UNESP]
dc.contributor.authorKawano, Paulo Roberto [UNESP]
dc.contributor.authorPadovani, Carlos Roberto [UNESP]
dc.contributor.authorLima, Flávio de Oliveira [UNESP]
dc.contributor.authorBernardes, Suene
dc.contributor.authorMagalhães, Eloá Siqueira [UNESP]
dc.contributor.authorAmaro, Carmen Regina Petean [UNESP]
dc.contributor.authorAmaro, João Luiz [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-27T11:29:53Z
dc.date.available2014-05-27T11:29:53Z
dc.date.issued2013-07-01
dc.description.abstractPurpose: To investigate nephrocalcinosis due to hyperoxaluria induced by two different inducing agents in rats. Methods: Forty Sprague-Dawley male rats were randomly distributed into four groups: Group1 (Clinical control, n = 10); Group 2 (0.5% Ethylene Glycol + Vitamin D3, n = 10); Group 3 (1.25% Ethylene Glycol, n = 10); and Group 4 (5%Hydroxy L-proline, n = 10). Five animals from each group were euthanized after one week of follow-up (M1 Moment) and the remaining, after four weeks (M2 Moment). All animals underwent 24h urine dosages of calcium, oxalate, uric acid, citrate and serum creatinine. Histology and histomorphometric analyses were performed using Image J program in the hematoxylin-eosin stains. Calcium deposits in the renal parenchyma were quantified by PIXE technique (Proton Induced X-Ray Emission). Results: 24h urinary parameters did not show any significant variations after 28 days of experiment except by hyperoxaluria that was significantly higher in Group 3. Histomorphometric analyses showed a significantly higher nephrocalcinosis in Group 2 (p<0.01). The calcium deposits in the renal parenchyma were 10 and 100 times higher in Group 2 in comparison to other groups in the M1 and M2 moments, respectively. Conclusion: The Group 2 (vitamin D3+Ethylene Glycol 0.5%) was the best model to induce nephrocalcinosis in rats after 28 days.en
dc.description.affiliationBotucatu School of Medicine São Paulo State University UNESP, Botucatu-SP
dc.description.affiliationDepartment of Urology Botucatu School of Medicine São Paulo State University, UNESP, Botucatu-SP
dc.description.affiliationDepartment of Biostatistics Botucatu Institute of Biosciences São Paulo State University, UNESP, Botucatu-SP
dc.description.affiliationDepartment of Pathology Botucatu School of Medicine São Paulo State University, UNESP, Botucatu-SP
dc.description.affiliationInstitute of Physics University of Sao Paulo (USP)
dc.description.affiliationIC FAPESP Botucatu Institute of Biosciences São Paulo State University, UNESP, Botucatu-SP
dc.description.affiliationUnespBotucatu School of Medicine São Paulo State University UNESP, Botucatu-SP
dc.description.affiliationUnespDepartment of Urology Botucatu School of Medicine São Paulo State University, UNESP, Botucatu-SP
dc.description.affiliationUnespDepartment of Biostatistics Botucatu Institute of Biosciences São Paulo State University, UNESP, Botucatu-SP
dc.description.affiliationUnespDepartment of Pathology Botucatu School of Medicine São Paulo State University, UNESP, Botucatu-SP
dc.description.affiliationUnespIC FAPESP Botucatu Institute of Biosciences São Paulo State University, UNESP, Botucatu-SP
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 11/116990
dc.format.extent496-501
dc.identifierhttp://dx.doi.org/10.1590/S0102-86502013000700004
dc.identifier.citationActa Cirurgica Brasileira, v. 28, n. 7, p. 496-501, 2013.
dc.identifier.doi10.1590/S0102-86502013000700004
dc.identifier.file2-s2.0-84880393431.pdf
dc.identifier.issn0102-8650
dc.identifier.issn1678-2674
dc.identifier.lattes2443296326760741
dc.identifier.lattes8727897080522289
dc.identifier.lattes9989857854355692
dc.identifier.orcid0000-0001-8411-5822
dc.identifier.scieloS0102-86502013000700004
dc.identifier.scopus2-s2.0-84880393431
dc.identifier.urihttp://hdl.handle.net/11449/75842
dc.identifier.wosWOS:000322407000004
dc.language.isoeng
dc.relation.ispartofActa Cirúrgica Brasileira
dc.relation.ispartofjcr0.933
dc.relation.ispartofsjr0,395
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectHyperoxaluria
dc.subjectLithiasis
dc.subjectNephrocalcinosis
dc.subjectRats
dc.subjectcalcium
dc.subjectcalcium oxalate
dc.subjectcitric acid
dc.subjectcreatinine
dc.subjectoxalic acid
dc.subjecturic acid
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectcontrolled study
dc.subjecthistology
dc.subjecthyperoxaluria
dc.subjectkidney calcification
dc.subjectkidney parenchyma
dc.subjectmale
dc.subjectmorphometrics
dc.subjectnonhuman
dc.subjectrat
dc.subjecturine pH
dc.subjecturine volume
dc.titleNephrocalcinosis induced by hyperoxaluria in ratsen
dc.typeArtigo
dcterms.licensehttp://www.scielo.br/revistas/acb/iaboutj.htm
dspace.entity.typePublication
unesp.author.lattes2443296326760741
unesp.author.lattes8727897080522289[3]
unesp.author.lattes9989857854355692[2]
unesp.author.orcid0000-0001-8411-5822[2]
unesp.author.orcid0000-0002-7719-9682[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentPatologia - FMBpt
unesp.departmentUrologia - FMBpt
unesp.departmentBioestatística - IBBpt

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