Efeito do betacaroteno sobre o estresse oxidativo e a expressão de conexina 43 cardíaca
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , |
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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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/openAccess2024-08-14T17:36:53Zoai:repositorio.unesp.br:11449/109808Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:36:53Repositório 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 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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 |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
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) |
repository.mail.fl_str_mv |
|
_version_ |
1808128206578909184 |