You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/32965
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSpadella, César Tadeu-
dc.contributor.authorMercadante, MCS-
dc.contributor.authorSchellini, Silvana Artioli-
dc.contributor.authorMachado, JLM-
dc.contributor.authorOliveira, Walmar Kerche de-
dc.contributor.authorBacchi, C. E.-
dc.date.accessioned2014-05-20T15:21:53Z-
dc.date.accessioned2016-10-25T17:55:26Z-
dc.date.available2014-05-20T15:21:53Z-
dc.date.available2016-10-25T17:55:26Z-
dc.date.issued1996-08-01-
dc.identifierhttp://www.scielo.br/scielo.php?script=sci_issues&pid=0100-879X&lng=en&nrm=iso-
dc.identifier.citationBrazilian Journal of Medical and Biological Research. São Paulo: Associação Bras Divulg Cientifica, v. 29, n. 8, p. 1019-1024, 1996.-
dc.identifier.issn0100-879X-
dc.identifier.urihttp://hdl.handle.net/11449/32965-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/32965-
dc.description.abstractWe studied the effects of pancreas transplantation on kidney lesions of rats with alloxan-induced diabetes. Ninety inbred male Lewis rats were randomly assigned to 3 experimental groups: group NC included 30 non-diabetic control rats, group DC included 30 alloxan-induced diabetic control rats, and group PT included 30 alloxan-induced diabetic rats that received pancreas transplants from normal donor Lewis rats. Each group was further divided into 3 subgroups of 10 rats which were sacrificed at 1, 3, and 6 months of follow-up, respectively. Clinical and laboratory parameters during these periods were documented. The kidneys of 5 rats in each subgroup were studied and 50 glomeruli and tubules from each kidney were analyzed by light microscopy by two different investigators in a double-blind study. There was progressive glomerular basement membrane thickening (GBMT), mesangial enlargement (ME), and Bowman's capsule thickening (BCT) in kidneys of rats in the 3 experimental groups during follow-up. These alterations were significantly higher in DC rats (GBMT: 1.99 +/- 0.31; ME: 2.00 +/- 0.33; BCT: 1.88 +/- 0.27) when compared to NC(GBMT: 1.54 +/- 0.30; ME: 1.56 +/- 0.47; BCT: 1.36 +/- 0.35) and PT rats (GBMT: 1.49 +/- 0.29; ME: 1.57 +/- 0.36; BCT: 1.35 +/- 0.28) at 6 months (P<0.01). The extent of GBMT, ME, and BCT observed in DC rats at 1 and 3 months was not significantly different from NC and PT rats. The amount of kidney lesions in PT rats was similar to that of NC rats and lower than those of DC rats at 6 months (P<0.01). In addition, Armanni-Ebstein lesions of the tubules (AE) and tubular lumen protein (PRO) observed in DC rats were not present in NC or PT rats. We conclude that pancreas transplantation in alloxan-induced diabetic rats prevents the development of kidney lesions beginning at 6 months after transplantation.en
dc.format.extent1019-1024-
dc.language.isoeng-
dc.publisherAssociação Brasileira de Divulgação Científica (ABRADIC)-
dc.sourceWeb of Science-
dc.subjectdiabetic nephropathypt
dc.subjectalloxan-induced diabetespt
dc.subjectpancreas transplantationpt
dc.titleEffect of pancreas transplantation on the prevention of nephropathy in alloxan-induced diabetic ratsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNIV ESTADUAL PAULISTA,FAC MED BOTUCATU,DEPT OFTALMOL & OTORRINOLARINGOL,BR-18618970 BOTUCATU,SP,BRAZIL-
dc.description.affiliationUNIV ESTADUAL PAULISTA,FAC MED BOTUCATU,DEPT PATOL,BR-18618970 BOTUCATU,SP,BRAZIL-
dc.description.affiliationUnespUNIV ESTADUAL PAULISTA,FAC MED BOTUCATU,DEPT OFTALMOL & OTORRINOLARINGOL,BR-18618970 BOTUCATU,SP,BRAZIL-
dc.description.affiliationUnespUNIV ESTADUAL PAULISTA,FAC MED BOTUCATU,DEPT PATOL,BR-18618970 BOTUCATU,SP,BRAZIL-
dc.identifier.wosWOS:A1996VD70600013-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofBrazilian Journal of Medical and Biological Research-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.