Redox-sensitive prosurvival and proapoptotic protein expression in the myocardial remodeling post-infarction in rats


Autoria(s): SCHENKEL, Paulo Cavalheiro; TAVARES, Angela Maria Vicente; FERNANDES, Rafael Oliveira; DINIZ, Gabriela Placona; BERTAGNOLLI, Mariane; ARAUJO, Alex Sander da Rosa; BARRETO-CHAVES, Maria Luiza; RIBEIRO, Maria Flavia Marques; CLAUSELL, Nadine; BELLO-KLEIN, Adriane
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

In this study, we investigated the oxidative stress influence in some prosurvival and proapoptotic proteins after myocardial infarction (MI). Male Wistar rats were divided in two groups: Sham-operated (control) and MI. MI was induced by left coronary artery occlusion. 28-days after surgery, echocardiographic, morphometric, and hemodynamic parameters were evaluated. Redox status (reduced to oxidized glutathione ratio, GSH/GSSG) and hydrogen peroxide levels (H(2)O(2)) were measured in heart tissue. The p-ERK/ERK, p-Akt/Akt, p-mTOR/mTOR and p-GSK-3 beta/GSK-3 beta ratios, as well as apoptosis-inducing factor (AIF) myocardial protein expression were quantified by Western blot. MI group showed an increase in cardiac hypertrophy (23%) associated with a decrease in ejection fraction (38%) and increase in left ventricular end-diastolic pressure (82%) when compared to control, characterizing ventricular dysfunction. Redox status imbalance was seen in MI animals, as evidenced by the decrease in the GSH/GSSG ratio (30%) and increased levels of H(2)O(2) (45%). This group also showed an increase in the ERK phosphorylation and a reduction of Akt and mTOR phosphorylation when compared to control. Moreover, we showed a reduction in the GSK-3 beta phosphorylation and an increase in AIF protein expression in MI group. Taken together, our results show increased H(2)O(2) levels and cellular redox imbalance associated to a higher p-ERK and AIF immunocontent, which would contribute to a maladaptive hypertrophy phenotype.

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Fundacao de Amparo a Pesquisa do Estado do Rio Grande do Sul (FAPERGS)

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul (FAPERGS)

Secretaria de Ciencia e Tecnologia do Estado do Rio Grande do Sul (SCT-RS)

Secretaria de Ciencia e Tecnologia do Estado do Rio Grande do Sul (SCT-RS)

Identificador

MOLECULAR AND CELLULAR BIOCHEMISTRY, v.341, n.1/Fev, p.1-8, 2010

0300-8177

http://producao.usp.br/handle/BDPI/27843

10.1007/s11010-010-0431-8

http://dx.doi.org/10.1007/s11010-010-0431-8

Idioma(s)

eng

Publicador

SPRINGER

Relação

Molecular and Cellular Biochemistry

Direitos

closedAccess

Copyright SPRINGER

Palavras-Chave #Akt #ERK #GSH/GSSG #Hydrogen peroxide #Myocardial infarction #Oxidative stress #HYDROGEN-PEROXIDE #OXIDATIVE STRESS #SIGNALING PATHWAYS #MYOCYTE APOPTOSIS #CELL-DEATH #EXPERIMENTAL HYPERTHYROIDISM #VENTRICULAR-FUNCTION #CARDIAC-HYPERTROPHY #HEART-FAILURE #INFARCT SIZE #Cell Biology
Tipo

article

original article

publishedVersion