Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats

Detalhes bibliográficos
Autor(a) principal: Ptilovanciv, Ellen O. N. [UNIFESP]
Data de Publicação: 2013
Outros Autores: Fernandes, Gabryelle S. [UNIFESP], Teixeira, Luciana C. [UNIFESP], Reis, Luciana A. [UNIFESP], Pessoa, Edson A. [UNIFESP], Convento, Marcia B. [UNIFESP], Simoes, Manuel J. [UNIFESP], Albertoni, Guilherme A. [UNIFESP], Schor, Nestor [UNIFESP], Borges, Fernanda T. [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1186/1758-5996-5-3
http://repositorio.unifesp.br/handle/11600/35880
Resumo: One important concern in the treatment of diabetes is the maintenance of glycemic levels and the prevention of diabetic nephropathy. Inducible heme oxygenase 1 (HO-1) is a rate-limiting enzyme thought to have antioxidant and cytoprotective roles. the goal of the present study was to analyze the effect of HO-1 induction in chronically hyperglycemic rats. the hyperglycemic rats were divided into two groups: one group, called STZ, was given a single injection of streptozotocin; and the other group was given a single streptozotocin injection as well as daily injections of hemin, an HO-1 inducer, over 60 days (STZ + HEME). A group of normoglycemic, untreated rats was used as the control (CTL).Body weight, diuresis, serum glucose levels, microalbuminuria, creatinine clearance rate, urea levels, sodium excretion, and lipid peroxidation were analyzed. Histological alterations and immunohistochemistry for HO-1 and inducible nitric oxide synthase (iNOS) were assessed. After 60 days, the STZ group exhibited an increase in blood glucose, diuresis, urea, microalbuminuria, and sodium excretion. There was no weight gain, and there was a decrease in creatinine clearance in comparison to the CTL group. in the STZ + HEME group there was an improvement in the metabolic parameters and kidney function, a decrease in blood glucose, serum urea, and microalbuminuria, and an increase of creatinine clearance, in comparison to the STZ group.There was glomerulosclerosis, collagen deposition in the STZ rats and increase in iNOS and HO-1 expression. in the STZ + HEME group, the glomerulosclerosis and fibrosis was prevented and there was an increase in the expression of HO-1, but decrease in iNOS expression and lipid peroxidation. in conclusion, our data suggest that chronic induction of HO-1 reduces hyperglycemia, improves glucose metabolism and, at least in part, protects the renal tissue from hyperglycemic injury, possibly through the antioxidant activity of HO-1.
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spelling Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic ratsHeme oxygenase 1Nitric oxide synthaseRenal functionDiabetic nephropathyGlucose metabolismOne important concern in the treatment of diabetes is the maintenance of glycemic levels and the prevention of diabetic nephropathy. Inducible heme oxygenase 1 (HO-1) is a rate-limiting enzyme thought to have antioxidant and cytoprotective roles. the goal of the present study was to analyze the effect of HO-1 induction in chronically hyperglycemic rats. the hyperglycemic rats were divided into two groups: one group, called STZ, was given a single injection of streptozotocin; and the other group was given a single streptozotocin injection as well as daily injections of hemin, an HO-1 inducer, over 60 days (STZ + HEME). A group of normoglycemic, untreated rats was used as the control (CTL).Body weight, diuresis, serum glucose levels, microalbuminuria, creatinine clearance rate, urea levels, sodium excretion, and lipid peroxidation were analyzed. Histological alterations and immunohistochemistry for HO-1 and inducible nitric oxide synthase (iNOS) were assessed. After 60 days, the STZ group exhibited an increase in blood glucose, diuresis, urea, microalbuminuria, and sodium excretion. There was no weight gain, and there was a decrease in creatinine clearance in comparison to the CTL group. in the STZ + HEME group there was an improvement in the metabolic parameters and kidney function, a decrease in blood glucose, serum urea, and microalbuminuria, and an increase of creatinine clearance, in comparison to the STZ group.There was glomerulosclerosis, collagen deposition in the STZ rats and increase in iNOS and HO-1 expression. in the STZ + HEME group, the glomerulosclerosis and fibrosis was prevented and there was an increase in the expression of HO-1, but decrease in iNOS expression and lipid peroxidation. in conclusion, our data suggest that chronic induction of HO-1 reduces hyperglycemia, improves glucose metabolism and, at least in part, protects the renal tissue from hyperglycemic injury, possibly through the antioxidant activity of HO-1.Universidade Federal de São Paulo UNIFESP, Div Nephrol, Dept Med, São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Morphol Dept, São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Div Nephrol, Dept Med, São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Morphol Dept, São Paulo, BrazilWeb of ScienceBiomed Central LtdUniversidade Federal de São Paulo (UNIFESP)Ptilovanciv, Ellen O. N. [UNIFESP]Fernandes, Gabryelle S. [UNIFESP]Teixeira, Luciana C. [UNIFESP]Reis, Luciana A. [UNIFESP]Pessoa, Edson A. [UNIFESP]Convento, Marcia B. [UNIFESP]Simoes, Manuel J. [UNIFESP]Albertoni, Guilherme A. [UNIFESP]Schor, Nestor [UNIFESP]Borges, Fernanda T. [UNIFESP]2016-01-24T14:31:08Z2016-01-24T14:31:08Z2013-01-16info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion8application/pdfhttp://dx.doi.org/10.1186/1758-5996-5-3Diabetology & Metabolic Syndrome. London: Biomed Central Ltd, v. 5, 8 p., 2013.10.1186/1758-5996-5-3WOS000314977200001.pdf1758-5996http://repositorio.unifesp.br/handle/11600/35880WOS:000314977200001engDiabetology & Metabolic Syndromeinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-01T05:06:51Zoai:repositorio.unifesp.br/:11600/35880Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-01T05:06:51Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats
title Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats
spellingShingle Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats
Ptilovanciv, Ellen O. N. [UNIFESP]
Heme oxygenase 1
Nitric oxide synthase
Renal function
Diabetic nephropathy
Glucose metabolism
title_short Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats
title_full Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats
title_fullStr Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats
title_full_unstemmed Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats
title_sort Heme oxygenase 1 improves glucoses metabolism and kidney histological alterations in diabetic rats
author Ptilovanciv, Ellen O. N. [UNIFESP]
author_facet Ptilovanciv, Ellen O. N. [UNIFESP]
Fernandes, Gabryelle S. [UNIFESP]
Teixeira, Luciana C. [UNIFESP]
Reis, Luciana A. [UNIFESP]
Pessoa, Edson A. [UNIFESP]
Convento, Marcia B. [UNIFESP]
Simoes, Manuel J. [UNIFESP]
Albertoni, Guilherme A. [UNIFESP]
Schor, Nestor [UNIFESP]
Borges, Fernanda T. [UNIFESP]
author_role author
author2 Fernandes, Gabryelle S. [UNIFESP]
Teixeira, Luciana C. [UNIFESP]
Reis, Luciana A. [UNIFESP]
Pessoa, Edson A. [UNIFESP]
Convento, Marcia B. [UNIFESP]
Simoes, Manuel J. [UNIFESP]
Albertoni, Guilherme A. [UNIFESP]
Schor, Nestor [UNIFESP]
Borges, Fernanda T. [UNIFESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Ptilovanciv, Ellen O. N. [UNIFESP]
Fernandes, Gabryelle S. [UNIFESP]
Teixeira, Luciana C. [UNIFESP]
Reis, Luciana A. [UNIFESP]
Pessoa, Edson A. [UNIFESP]
Convento, Marcia B. [UNIFESP]
Simoes, Manuel J. [UNIFESP]
Albertoni, Guilherme A. [UNIFESP]
Schor, Nestor [UNIFESP]
Borges, Fernanda T. [UNIFESP]
dc.subject.por.fl_str_mv Heme oxygenase 1
Nitric oxide synthase
Renal function
Diabetic nephropathy
Glucose metabolism
topic Heme oxygenase 1
Nitric oxide synthase
Renal function
Diabetic nephropathy
Glucose metabolism
description One important concern in the treatment of diabetes is the maintenance of glycemic levels and the prevention of diabetic nephropathy. Inducible heme oxygenase 1 (HO-1) is a rate-limiting enzyme thought to have antioxidant and cytoprotective roles. the goal of the present study was to analyze the effect of HO-1 induction in chronically hyperglycemic rats. the hyperglycemic rats were divided into two groups: one group, called STZ, was given a single injection of streptozotocin; and the other group was given a single streptozotocin injection as well as daily injections of hemin, an HO-1 inducer, over 60 days (STZ + HEME). A group of normoglycemic, untreated rats was used as the control (CTL).Body weight, diuresis, serum glucose levels, microalbuminuria, creatinine clearance rate, urea levels, sodium excretion, and lipid peroxidation were analyzed. Histological alterations and immunohistochemistry for HO-1 and inducible nitric oxide synthase (iNOS) were assessed. After 60 days, the STZ group exhibited an increase in blood glucose, diuresis, urea, microalbuminuria, and sodium excretion. There was no weight gain, and there was a decrease in creatinine clearance in comparison to the CTL group. in the STZ + HEME group there was an improvement in the metabolic parameters and kidney function, a decrease in blood glucose, serum urea, and microalbuminuria, and an increase of creatinine clearance, in comparison to the STZ group.There was glomerulosclerosis, collagen deposition in the STZ rats and increase in iNOS and HO-1 expression. in the STZ + HEME group, the glomerulosclerosis and fibrosis was prevented and there was an increase in the expression of HO-1, but decrease in iNOS expression and lipid peroxidation. in conclusion, our data suggest that chronic induction of HO-1 reduces hyperglycemia, improves glucose metabolism and, at least in part, protects the renal tissue from hyperglycemic injury, possibly through the antioxidant activity of HO-1.
publishDate 2013
dc.date.none.fl_str_mv 2013-01-16
2016-01-24T14:31:08Z
2016-01-24T14:31:08Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/1758-5996-5-3
Diabetology & Metabolic Syndrome. London: Biomed Central Ltd, v. 5, 8 p., 2013.
10.1186/1758-5996-5-3
WOS000314977200001.pdf
1758-5996
http://repositorio.unifesp.br/handle/11600/35880
WOS:000314977200001
url http://dx.doi.org/10.1186/1758-5996-5-3
http://repositorio.unifesp.br/handle/11600/35880
identifier_str_mv Diabetology & Metabolic Syndrome. London: Biomed Central Ltd, v. 5, 8 p., 2013.
10.1186/1758-5996-5-3
WOS000314977200001.pdf
1758-5996
WOS:000314977200001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Diabetology & Metabolic Syndrome
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 8
application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd
publisher.none.fl_str_mv Biomed Central Ltd
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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