Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca

Detalhes bibliográficos
Autor(a) principal: Novo, Rosangela [UNESP]
Data de Publicação: 2013
Outros Autores: Gaiolla, Paula Schmidt Azevedo [UNESP], Minicucci, Marcos Ferreira [UNESP], Zornoff, Leonardo Antonio Mamede [UNESP], Paiva, Sergio Alberto Rupp de [UNESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.5935/abc.20130160
http://hdl.handle.net/11449/109808
Resumo: BACKGROUND: Intervention studies have shown an increased mortality in patients who received beta-carotene. However, the mechanisms involved in this phenomenon are still unknown. OBJECTIVE: Evaluate the influence of beta-carotene on oxidative stress and the expression of connexin 43 in rat hearts. METHODS: Wistar rats, weighing approximately 100 g, were allocated in two groups: Control Group (n=30), that received the diet routinely used in our laboratory, and Beta-Carotene Group (n = 28), which received beta-carotene (in crystal form, added and mixed to the diet) at a dose of 500 mg of beta-carotene/kg of diet. The animals received the treatment until they reached 200-250g, when they were sacrificed. Samples of blood, liver and heart were collected to perform Western blotting and immunohistochemistry for connexin 43; morphometric studies, dosages of beta-carotene by high-performance liquid chromatography as well as reduced glutathione, oxidized glutathione and lipids hydroperoxides were performed by biochemical analysis. RESULTS: Beta-carotene was detected only in the liver of Beta-Carotene Group animals (288 ± 94.7 µg/kg). Levels of reduced/oxidized glutathione were higher in the liver and heart of Beta-Carotene Group animals (liver - Control Group: 42.60 ± 1.62; liver - Beta-Carotene Group: 57.40 ± 5.90; p = 0.04; heart: - Control Group: 117.40 ± 1.01; heart - Beta-Carotene Group: 121.81 ± 1.32 nmol/mg protein; p = 0.03). The content of total connexin 43 was larger in Beta-Carotene Group. CONCLUSION: Beta-carotene demonstrated a positive effect, characterized by the increase of intercellular communication and improvement of anti-oxidizing defense system. In this model, mechanism does not explain the increased mortality rate observed with the beta-carotene supplementation in clinical studies. (Arq Bras Cardiol. 2013; [online].ahead print, PP.0-0)
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spelling Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíacaEffect of beta-carotene on oxidative stress and expression of cardiac connexin 43Beta CarotenoEstresse OxidativoRatosConexina 43Remodelação VentricularBeta CaroteneOxidative StressRatsVentricular RemodelingBACKGROUND: Intervention studies have shown an increased mortality in patients who received beta-carotene. However, the mechanisms involved in this phenomenon are still unknown. OBJECTIVE: Evaluate the influence of beta-carotene on oxidative stress and the expression of connexin 43 in rat hearts. METHODS: Wistar rats, weighing approximately 100 g, were allocated in two groups: Control Group (n=30), that received the diet routinely used in our laboratory, and Beta-Carotene Group (n = 28), which received beta-carotene (in crystal form, added and mixed to the diet) at a dose of 500 mg of beta-carotene/kg of diet. The animals received the treatment until they reached 200-250g, when they were sacrificed. Samples of blood, liver and heart were collected to perform Western blotting and immunohistochemistry for connexin 43; morphometric studies, dosages of beta-carotene by high-performance liquid chromatography as well as reduced glutathione, oxidized glutathione and lipids hydroperoxides were performed by biochemical analysis. RESULTS: Beta-carotene was detected only in the liver of Beta-Carotene Group animals (288 ± 94.7 µg/kg). Levels of reduced/oxidized glutathione were higher in the liver and heart of Beta-Carotene Group animals (liver - Control Group: 42.60 ± 1.62; liver - Beta-Carotene Group: 57.40 ± 5.90; p = 0.04; heart: - Control Group: 117.40 ± 1.01; heart - Beta-Carotene Group: 121.81 ± 1.32 nmol/mg protein; p = 0.03). The content of total connexin 43 was larger in Beta-Carotene Group. CONCLUSION: Beta-carotene demonstrated a positive effect, characterized by the increase of intercellular communication and improvement of anti-oxidizing defense system. In this model, mechanism does not explain the increased mortality rate observed with the beta-carotene supplementation in clinical studies. (Arq Bras Cardiol. 2013; [online].ahead print, PP.0-0)FUNDAMENTO: Estudos de intervenção mostraram aumento da mortalidade em pacientes que receberam betacaroteno. Contudo, não são conhecidos os mecanismos envolvidos nesse fenômeno. OBJETIVO: Avaliar a influência do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 em coração de ratos. MÉTODOS: Ratos Wistar, pesando aproximadamente 100 g, foram alocados em dois grupos: Grupo Controle (n = 30), que recebeu a dieta usada de rotina em nosso laboratório, e Grupo Betacaroteno (n = 28), que recebeu betacaroteno (na forma de cristal, adicionado e misturado à dieta) na dose de 500 mg de betacaroteno/kg de dieta. Os animais receberam tratamento até que atingissem entre 200 e 250 g, quando eram sacrificados. Foram coletados sangue, fígado e coração para realização de Western blotting e imunoistoquímica para conexina 43; foram realizados estudos morfométricos, dosagens de betacaroteno por cromatografia líquida de alta eficiência bem como de glutationa reduzida, glutationa oxidada e hidroperóxidos de lipídeos por análises bioquímicas. RESULTADOS: O betacaroteno foi detectado apenas no fígado dos animais do Grupo Betacaroteno (288 ± 94,7 µg/kg). Os níveis de glutationa reduzida/glutationa oxidada foram maiores no fígado e no coração dos animais do Grupo Betacaroteno (fígado - Grupo Controle: 42,60 ± 1,62; fígado - Grupo Betacaroteno: 57,40 ± 5,90; p = 0,04; coração: - Grupo Controle: 117,40 ± 1,01; coração - Grupo Betacaroteno: 121,81 ± 1,32 nmol/mg proteína; p = 0,03). O conteúdo de conexina 43 total foi maior no Grupo Betacaroteno. CONCLUSÃO: O betacaroteno apresentou efeito benéfico, caracterizado pelo aumento da comunicação intercelular e melhora do sistema de defesa antioxidante. Nesse modelo, os mecanismos não explicam a maior mortalidade observada com a suplementação de betacaroteno em estudos clínicos. (Arq Bras Cardiol. 2013; [online].ahead print, PP.0-0)Universidade Estadual Paulista Júlio de Mesquita Filho Faculdade de Medicina de BotucatuUniversidade Estadual Paulista Júlio de Mesquita Filho Faculdade de Medicina de BotucatuSociedade Brasileira de Cardiologia (SBC)Universidade Estadual Paulista (Unesp)Novo, Rosangela [UNESP]Gaiolla, Paula Schmidt Azevedo [UNESP]Minicucci, Marcos Ferreira [UNESP]Zornoff, Leonardo Antonio Mamede [UNESP]Paiva, Sergio Alberto Rupp de [UNESP]2014-10-01T13:08:34Z2014-10-01T13:08:34Z2013-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article233-239application/pdfhttp://dx.doi.org/10.5935/abc.20130160Arquivos Brasileiros de Cardiologia. Sociedade Brasileira de Cardiologia - SBC, v. 101, n. 3, p. 233-239, 2013.0066-782Xhttp://hdl.handle.net/11449/10980810.5935/abc.20130160S0066-782X2013002900007WOS:0003249132000122-s2.0-84884748320S0066-782X2013002900007.pdf5016839015394547121314080140264774387040344716730000-0002-5843-6232SciELOreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporArquivos Brasileiros de Cardiologia1.318info:eu-repo/semantics/openAccess2024-01-19T06:27:05Zoai:repositorio.unesp.br:11449/109808Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-19T06:27:05Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
Effect of beta-carotene on oxidative stress and expression of cardiac connexin 43
title Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
spellingShingle Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
Novo, Rosangela [UNESP]
Beta Caroteno
Estresse Oxidativo
Ratos
Conexina 43
Remodelação Ventricular
Beta Carotene
Oxidative Stress
Rats
Ventricular Remodeling
title_short Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
title_full Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
title_fullStr Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
title_full_unstemmed Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
title_sort Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
author Novo, Rosangela [UNESP]
author_facet Novo, Rosangela [UNESP]
Gaiolla, Paula Schmidt Azevedo [UNESP]
Minicucci, Marcos Ferreira [UNESP]
Zornoff, Leonardo Antonio Mamede [UNESP]
Paiva, Sergio Alberto Rupp de [UNESP]
author_role author
author2 Gaiolla, Paula Schmidt Azevedo [UNESP]
Minicucci, Marcos Ferreira [UNESP]
Zornoff, Leonardo Antonio Mamede [UNESP]
Paiva, Sergio Alberto Rupp de [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Novo, Rosangela [UNESP]
Gaiolla, Paula Schmidt Azevedo [UNESP]
Minicucci, Marcos Ferreira [UNESP]
Zornoff, Leonardo Antonio Mamede [UNESP]
Paiva, Sergio Alberto Rupp de [UNESP]
dc.subject.por.fl_str_mv Beta Caroteno
Estresse Oxidativo
Ratos
Conexina 43
Remodelação Ventricular
Beta Carotene
Oxidative Stress
Rats
Ventricular Remodeling
topic Beta Caroteno
Estresse Oxidativo
Ratos
Conexina 43
Remodelação Ventricular
Beta Carotene
Oxidative Stress
Rats
Ventricular Remodeling
description BACKGROUND: Intervention studies have shown an increased mortality in patients who received beta-carotene. However, the mechanisms involved in this phenomenon are still unknown. OBJECTIVE: Evaluate the influence of beta-carotene on oxidative stress and the expression of connexin 43 in rat hearts. METHODS: Wistar rats, weighing approximately 100 g, were allocated in two groups: Control Group (n=30), that received the diet routinely used in our laboratory, and Beta-Carotene Group (n = 28), which received beta-carotene (in crystal form, added and mixed to the diet) at a dose of 500 mg of beta-carotene/kg of diet. The animals received the treatment until they reached 200-250g, when they were sacrificed. Samples of blood, liver and heart were collected to perform Western blotting and immunohistochemistry for connexin 43; morphometric studies, dosages of beta-carotene by high-performance liquid chromatography as well as reduced glutathione, oxidized glutathione and lipids hydroperoxides were performed by biochemical analysis. RESULTS: Beta-carotene was detected only in the liver of Beta-Carotene Group animals (288 ± 94.7 µg/kg). Levels of reduced/oxidized glutathione were higher in the liver and heart of Beta-Carotene Group animals (liver - Control Group: 42.60 ± 1.62; liver - Beta-Carotene Group: 57.40 ± 5.90; p = 0.04; heart: - Control Group: 117.40 ± 1.01; heart - Beta-Carotene Group: 121.81 ± 1.32 nmol/mg protein; p = 0.03). The content of total connexin 43 was larger in Beta-Carotene Group. CONCLUSION: Beta-carotene demonstrated a positive effect, characterized by the increase of intercellular communication and improvement of anti-oxidizing defense system. In this model, mechanism does not explain the increased mortality rate observed with the beta-carotene supplementation in clinical studies. (Arq Bras Cardiol. 2013; [online].ahead print, PP.0-0)
publishDate 2013
dc.date.none.fl_str_mv 2013-09-01
2014-10-01T13:08:34Z
2014-10-01T13:08:34Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.5935/abc.20130160
Arquivos Brasileiros de Cardiologia. Sociedade Brasileira de Cardiologia - SBC, v. 101, n. 3, p. 233-239, 2013.
0066-782X
http://hdl.handle.net/11449/109808
10.5935/abc.20130160
S0066-782X2013002900007
WOS:000324913200012
2-s2.0-84884748320
S0066-782X2013002900007.pdf
5016839015394547
1213140801402647
7438704034471673
0000-0002-5843-6232
url http://dx.doi.org/10.5935/abc.20130160
http://hdl.handle.net/11449/109808
identifier_str_mv Arquivos Brasileiros de Cardiologia. Sociedade Brasileira de Cardiologia - SBC, v. 101, n. 3, p. 233-239, 2013.
0066-782X
10.5935/abc.20130160
S0066-782X2013002900007
WOS:000324913200012
2-s2.0-84884748320
S0066-782X2013002900007.pdf
5016839015394547
1213140801402647
7438704034471673
0000-0002-5843-6232
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Arquivos Brasileiros de Cardiologia
1.318
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dc.format.none.fl_str_mv 233-239
application/pdf
dc.publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia (SBC)
publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia (SBC)
dc.source.none.fl_str_mv SciELO
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
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institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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