The Antiapoptotic Effect of Granulocyte Colony-stimulating Factor Reduces Infarct Size and Prevents Heart Failure Development in Rats


Autoria(s): BALDO, Marcelo P.; DAVEL, Ana P. C.; DAMAS-SOUZA, Danilo M.; NICOLETTI-CARVALHO, Jose E.; BORDIN, Silvana; CARVALHO, Hernandes F.; RODRIGUES, Sergio L.; ROSSONI, Luciana V.; MILL, Jose G.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Background/Aim. Granulocyte colony-stimulating factor (G-CSF) reduces myocardial injury and improves cardiac function after myocardial infarction (MI). We investigated the early alterations provided by G-CSF and the chronic repercussions in infarcted rats. Methods. Male Wistar rats (200-250g) received vehicle (MI) or G-CSF (MI-GCSF) (50 mu g/kg, sc) at 7, 3 and 1 days before MI surgery. Afterwards MI was produced and infarct size was measured 1 and 15 days after surgery. Expression of anti-and proapoptotic proteins was evaluated immediately before surgery. 24 hours after surgery, apoptotic nuclei were evaluated. Two weeks after MI, left ventricular (LV) function was evaluated, followed by in situ LV diastolic pressure-volume evaluation. Results. Infarct size was decreased by 1 day pretreatment before occlusion (36 +/- 2.8 vs. 44 +/- 2.1% in MI; P<0.05) and remained reduced at 15 days after infarction (28 +/- 2.2 vs. 36 +/- 1.4% in MI; P<0.05). G-CSF pretreatment increased Bcl-2 and Bcl-xL protein expression, but did not alter Bax in LV. Apoptotic nuclei were reduced by treatment (Sham: 0.46 +/- 0.42, MI: 15.5 +/- 2.43, MI-GCSF: 5.34 +/- 3.34%; P<0.05). Fifteen days after MI, cardiac function remained preserved in G-CSF pretreated rats. The LV dilation was reduced in MI-G-CSF group as compared to MI rats, being closely associated with infarct size. Conclusion. The early beneficial effects of G-CSF were essentials to preserve cardiac function at a chronic stage of myocardial infarction. Copyright (C) 2011 S. Karger AG, Basel

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Fundacao de Amparo a Pesquisa do Espirito Santo - Pronex (FAPES)

Fundacao de Amparo a Pesquisa do Espirito Santo - Pronex (FAPES)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Identificador

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, v.28, n.1, p.33-40, 2011

1015-8987

http://producao.usp.br/handle/BDPI/27995

10.1159/000331711

http://dx.doi.org/10.1159/000331711

Idioma(s)

eng

Publicador

KARGER

Relação

Cellular Physiology and Biochemistry

Direitos

restrictedAccess

Copyright KARGER

Palavras-Chave #G-CSF #Myocardial infarction #Apoptosis #Chamber dilation #Heart failure #ACUTE MYOCARDIAL-INFARCTION #BONE-MARROW-CELLS #G-CSF #REPERFUSION INJURY #CARDIAC-FUNCTION #REPAIR #INHIBITION #THERAPY #CARDIOMYOCYTES #EXPANSION #Cell Biology #Physiology
Tipo

article

original article

publishedVersion