Progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic rats

We studied the effects of islet of Langerhans transplantation (IT) on the kidney lesions of rats with alloxan-induced diabetes. Forty-five inbred male Lewis rats were randomly assigned to 3 experimental groups: group Gl included 15 non-diabetic control rats (NC), group GIT included 15 alloxan-induced diabetic rats (DC), and group III included 15 alloxan-induced diabetic rats that received pancreatic islet transplantation prepared by nonenzymatic method from normal donor Lewis rats and injected into the portal vein (IT). Each group was further divided into 3 subgroups of 5 rats which were sacrificed at 1, 3, and 6 months of follow-up, respectively. Clinical and laboratorial parameters were recorded in the mentioned periods in the 3 experimental groups. For histology, the kidneys of all rats of each subgroup were studied and 50 glomeruli and 50 tubules of each kidney were analyzed using light microscopy by two different investigators in a double blind study. The results showed progressive glomerular basement membrane thickening (GBMT), mesangial enlargement (ME), and Bowman's capsule thickening (BCT) in the 3 experimental groups throughout the follow-up. These alterations were significantly more severe in DC rats at 6 months when compared to NC rats (p < 0.01). However, the degree of GBMT, ME, and BCT observed in DC rats was not statistically different from IT rats at 1, 3, and 6 months. In addition, Armanni-Ebstein lesions of the tubules (AE) and tubular lumen protein (PRO) observed in DC rats were also observed in IT rats all over the study. These lesions were never present in NC rats. We conclude that IT did not prevent progression of kidney lesions in alloxan-induced diabetic rats within 6 months after transplantation.

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Main Authors: Spadella,César Tadeu, Mercadante,Maria Cecília Salgado, Breim,Luiz Carlos, Macedo,Célia Sperandéo de, Bacchi,Carlos Eduardo, Macedo,Arthur Roquete de
Format: Digital revista
Language:English
Published: Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 1997
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86501997000100003
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spelling oai:scielo:S0102-865019970001000032010-12-01Progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic ratsSpadella,César TadeuMercadante,Maria Cecília SalgadoBreim,Luiz CarlosMacedo,Célia Sperandéo deBacchi,Carlos EduardoMacedo,Arthur Roquete de Islet transplantation Diabetic nephropathy Alloxan-induced-diabetes We studied the effects of islet of Langerhans transplantation (IT) on the kidney lesions of rats with alloxan-induced diabetes. Forty-five inbred male Lewis rats were randomly assigned to 3 experimental groups: group Gl included 15 non-diabetic control rats (NC), group GIT included 15 alloxan-induced diabetic rats (DC), and group III included 15 alloxan-induced diabetic rats that received pancreatic islet transplantation prepared by nonenzymatic method from normal donor Lewis rats and injected into the portal vein (IT). Each group was further divided into 3 subgroups of 5 rats which were sacrificed at 1, 3, and 6 months of follow-up, respectively. Clinical and laboratorial parameters were recorded in the mentioned periods in the 3 experimental groups. For histology, the kidneys of all rats of each subgroup were studied and 50 glomeruli and 50 tubules of each kidney were analyzed using light microscopy by two different investigators in a double blind study. The results showed progressive glomerular basement membrane thickening (GBMT), mesangial enlargement (ME), and Bowman's capsule thickening (BCT) in the 3 experimental groups throughout the follow-up. These alterations were significantly more severe in DC rats at 6 months when compared to NC rats (p < 0.01). However, the degree of GBMT, ME, and BCT observed in DC rats was not statistically different from IT rats at 1, 3, and 6 months. In addition, Armanni-Ebstein lesions of the tubules (AE) and tubular lumen protein (PRO) observed in DC rats were also observed in IT rats all over the study. These lesions were never present in NC rats. We conclude that IT did not prevent progression of kidney lesions in alloxan-induced diabetic rats within 6 months after transplantation.info:eu-repo/semantics/openAccessSociedade Brasileira para o Desenvolvimento da Pesquisa em CirurgiaActa Cirúrgica Brasileira v.12 n.1 19971997-03-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86501997000100003en10.1590/S0102-86501997000100003
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region America del Sur
libraryname SciELO
language English
format Digital
author Spadella,César Tadeu
Mercadante,Maria Cecília Salgado
Breim,Luiz Carlos
Macedo,Célia Sperandéo de
Bacchi,Carlos Eduardo
Macedo,Arthur Roquete de
spellingShingle Spadella,César Tadeu
Mercadante,Maria Cecília Salgado
Breim,Luiz Carlos
Macedo,Célia Sperandéo de
Bacchi,Carlos Eduardo
Macedo,Arthur Roquete de
Progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic rats
author_facet Spadella,César Tadeu
Mercadante,Maria Cecília Salgado
Breim,Luiz Carlos
Macedo,Célia Sperandéo de
Bacchi,Carlos Eduardo
Macedo,Arthur Roquete de
author_sort Spadella,César Tadeu
title Progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic rats
title_short Progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic rats
title_full Progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic rats
title_fullStr Progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic rats
title_full_unstemmed Progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic rats
title_sort progression of nephropathy after islet of langerhans transplantation in alloxan-induced diabetic rats
description We studied the effects of islet of Langerhans transplantation (IT) on the kidney lesions of rats with alloxan-induced diabetes. Forty-five inbred male Lewis rats were randomly assigned to 3 experimental groups: group Gl included 15 non-diabetic control rats (NC), group GIT included 15 alloxan-induced diabetic rats (DC), and group III included 15 alloxan-induced diabetic rats that received pancreatic islet transplantation prepared by nonenzymatic method from normal donor Lewis rats and injected into the portal vein (IT). Each group was further divided into 3 subgroups of 5 rats which were sacrificed at 1, 3, and 6 months of follow-up, respectively. Clinical and laboratorial parameters were recorded in the mentioned periods in the 3 experimental groups. For histology, the kidneys of all rats of each subgroup were studied and 50 glomeruli and 50 tubules of each kidney were analyzed using light microscopy by two different investigators in a double blind study. The results showed progressive glomerular basement membrane thickening (GBMT), mesangial enlargement (ME), and Bowman's capsule thickening (BCT) in the 3 experimental groups throughout the follow-up. These alterations were significantly more severe in DC rats at 6 months when compared to NC rats (p < 0.01). However, the degree of GBMT, ME, and BCT observed in DC rats was not statistically different from IT rats at 1, 3, and 6 months. In addition, Armanni-Ebstein lesions of the tubules (AE) and tubular lumen protein (PRO) observed in DC rats were also observed in IT rats all over the study. These lesions were never present in NC rats. We conclude that IT did not prevent progression of kidney lesions in alloxan-induced diabetic rats within 6 months after transplantation.
publisher Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia
publishDate 1997
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86501997000100003
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