Increased activities of cardiac matrix metalloproteinases matrix metalloproteinase (MMP)-2 and MMP-9 are associated with mortality during the acute phase of experimental Trypanosoma cruzi infection


Autoria(s): GUTIERREZ, Fredy Roberto Salazar; LALU, Manoj Mathew; MARIANO, Flavia Sammartino; MILANEZI, Cristiane Maria; CENA, Jonathan; GERLACH, Raquel Fernanda; SANTOS, Jose Eduardo Tanus; TORRES-DUENAS, Diego; CUNHA, Fernando Queiroz; SCHULZ, Richard; SILVA, Joao Santana
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

The strong inflammatory reaction that occurs in the heart during the acute phase of Trypanosoma cruzi infection is modulated by cytokines and chemokines produced by leukocytes and cardiomyocytes. Matrix metalloproteinases (MMPs) have recently emerged as modulators of cardiovascular inflammation. In the present study we investigated the role of MMP-2 and MMP-9 in T. cruzi-induced myocarditis, by use of immunohistochemical analysis, gelatin zymography, enzyme-linked immunosorbent assay, and real-time polymerase chain reaction to analyze the cardiac tissues of T. cruzi-infected C57BL/6 mice. Increased transcripts levels, immunoreactivity, and enzymatic activity for MMP-2 and MMP-9 were observed by day 14 after infection. Mice treated with an MMP inhibitor showed significantly decreased heart inflammation, delayed peak in parasitemia, and improved survival rates, compared with the control group. Reduced levels of cardiac tumor necrosis factor-alpha, interferon-gamma, serum nitrite, and serum nitrate were also observed in the treated group. These results suggest an important role for MMPs in the induction of T. cruzi-induced acute myocarditis.

Identificador

JOURNAL OF INFECTIOUS DISEASES, v.197, n.10, p.1468-1476, 2008

0022-1899

http://producao.usp.br/handle/BDPI/24247

10.1086/587487

http://dx.doi.org/10.1086/587487

Idioma(s)

eng

Publicador

UNIV CHICAGO PRESS

Relação

Journal of Infectious Diseases

Direitos

restrictedAccess

Copyright UNIV CHICAGO PRESS

Palavras-Chave #ISCHEMIA-REPERFUSION INJURY #CHAGAS HEART-DISEASE #GELATINASE-B #INTERFERON-GAMMA #NITRIC-OXIDE #GENE-EXPRESSION #TGF-BETA #IN-VITRO #MICE #DOXYCYCLINE #Immunology #Infectious Diseases #Microbiology
Tipo

article

original article

publishedVersion