Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas disease

Chagas disease, caused by Trypanosoma cruzi, represents an endemic among Latin America countries. The participation of free radicals, especially nitric oxide (NO), has been demonstrated in the pathophysiology of seropositive individuals with T. cruzi. In Chagas disease, increased NO contributes to t...

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Main Authors: Martha Elba Gonzalez-Mejia, Enrique Torres-Rasgado, Leonardo M Porchia, Hilda Rosas Salgado, José-Luis Totolhua, Arturo Ortega, Luisa Clara Regina Hernández-Kelly, Guadalupe Ruiz-Vivanco, Blanca G Báez-Duarte, Ricardo Pérez-Fuentes
Format: Article
Language:English
Published: Fundação Oswaldo Cruz (FIOCRUZ) 2014-04-01
Series:Memorias do Instituto Oswaldo Cruz
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762014000200174&lng=en&tlng=en
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author Martha Elba Gonzalez-Mejia
Enrique Torres-Rasgado
Leonardo M Porchia
Hilda Rosas Salgado
José-Luis Totolhua
Arturo Ortega
Luisa Clara Regina Hernández-Kelly
Guadalupe Ruiz-Vivanco
Blanca G Báez-Duarte
Ricardo Pérez-Fuentes
author_facet Martha Elba Gonzalez-Mejia
Enrique Torres-Rasgado
Leonardo M Porchia
Hilda Rosas Salgado
José-Luis Totolhua
Arturo Ortega
Luisa Clara Regina Hernández-Kelly
Guadalupe Ruiz-Vivanco
Blanca G Báez-Duarte
Ricardo Pérez-Fuentes
author_sort Martha Elba Gonzalez-Mejia
collection DOAJ
description Chagas disease, caused by Trypanosoma cruzi, represents an endemic among Latin America countries. The participation of free radicals, especially nitric oxide (NO), has been demonstrated in the pathophysiology of seropositive individuals with T. cruzi. In Chagas disease, increased NO contributes to the development of cardiomyopathy and megacolon. Metallothioneins (MTs) are efficient free radicals scavengers of NO in vitro and in vivo. Here, we developed a murine model of the chronic phase of Chagas disease using endemic T. cruzi RyCH1 in BALB/c mice, which were divided into four groups: infected non-treated (Inf), infected N-monomethyl-L-arginine treated (Inf L-NAME), non-infected L-NAME treated and non-infected vehicle-treated. We determined blood parasitaemia and NO levels, the extent of parasite nests in tissues and liver MT-I expression levels. It was observed that NO levels were increasing in Inf mice in a time-dependent manner. Inf L-NAME mice had fewer T. cruzi nests in cardiac and skeletal muscle with decreased blood NO levels at day 135 post infection. This affect was negatively correlated with an increase of MT-I expression (r = -0.8462, p < 0.0001). In conclusion, we determined that in Chagas disease, an unknown inhibitory mechanism reduces MT-I expression, allowing augmented NO levels.
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spelling doaj.art-2abf1708409344298d64da51b64d2ad52023-09-03T09:11:45ZengFundação Oswaldo Cruz (FIOCRUZ)Memorias do Instituto Oswaldo Cruz1678-80602014-04-01109217418110.1590/0074-0276140339S0074-02762014000200174Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas diseaseMartha Elba Gonzalez-MejiaEnrique Torres-RasgadoLeonardo M PorchiaHilda Rosas SalgadoJosé-Luis TotolhuaArturo OrtegaLuisa Clara Regina Hernández-KellyGuadalupe Ruiz-VivancoBlanca G Báez-DuarteRicardo Pérez-FuentesChagas disease, caused by Trypanosoma cruzi, represents an endemic among Latin America countries. The participation of free radicals, especially nitric oxide (NO), has been demonstrated in the pathophysiology of seropositive individuals with T. cruzi. In Chagas disease, increased NO contributes to the development of cardiomyopathy and megacolon. Metallothioneins (MTs) are efficient free radicals scavengers of NO in vitro and in vivo. Here, we developed a murine model of the chronic phase of Chagas disease using endemic T. cruzi RyCH1 in BALB/c mice, which were divided into four groups: infected non-treated (Inf), infected N-monomethyl-L-arginine treated (Inf L-NAME), non-infected L-NAME treated and non-infected vehicle-treated. We determined blood parasitaemia and NO levels, the extent of parasite nests in tissues and liver MT-I expression levels. It was observed that NO levels were increasing in Inf mice in a time-dependent manner. Inf L-NAME mice had fewer T. cruzi nests in cardiac and skeletal muscle with decreased blood NO levels at day 135 post infection. This affect was negatively correlated with an increase of MT-I expression (r = -0.8462, p < 0.0001). In conclusion, we determined that in Chagas disease, an unknown inhibitory mechanism reduces MT-I expression, allowing augmented NO levels.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762014000200174&lng=en&tlng=enmetallothionein-Iantioxidantsnitric oxideL-NAMEChagas disease
spellingShingle Martha Elba Gonzalez-Mejia
Enrique Torres-Rasgado
Leonardo M Porchia
Hilda Rosas Salgado
José-Luis Totolhua
Arturo Ortega
Luisa Clara Regina Hernández-Kelly
Guadalupe Ruiz-Vivanco
Blanca G Báez-Duarte
Ricardo Pérez-Fuentes
Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas disease
Memorias do Instituto Oswaldo Cruz
metallothionein-I
antioxidants
nitric oxide
L-NAME
Chagas disease
title Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas disease
title_full Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas disease
title_fullStr Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas disease
title_full_unstemmed Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas disease
title_short Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas disease
title_sort metallothionein 1 and nitric oxide expression are inversely correlated in a murine model of chagas disease
topic metallothionein-I
antioxidants
nitric oxide
L-NAME
Chagas disease
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762014000200174&lng=en&tlng=en
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