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Metallothionein-1 and nitric oxide expression are inversely correlated in a murine model of Chagas disease
Gonzalez-Mejia, Martha Elba; Torres-Rasgado, Enrique; Porchia, Leonardo M; Salgado, Hilda Rosas; Totolhua, José-Luis; Ortega, Arturo; Hernández-Kelly, Luisa Clara Regina; Ruiz-Vivanco, Guadalupe; Báez-Duarte, Blanca G; Pérez-Fuentes, Ricardo.
Afiliação
  • Gonzalez-Mejia, Martha Elba; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Torres-Rasgado, Enrique; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Porchia, Leonardo M; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Salgado, Hilda Rosas; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Totolhua, José-Luis; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Ortega, Arturo; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Hernández-Kelly, Luisa Clara Regina; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Ruiz-Vivanco, Guadalupe; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Báez-Duarte, Blanca G; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
  • Pérez-Fuentes, Ricardo; Benemérita Universidad Autónoma de Puebla. Facultad de Medicina. MX
Mem. Inst. Oswaldo Cruz ; 109(2): 174-181, abr. 2014. tab, graf
Article em En | LILACS | ID: lil-705826
Biblioteca responsável: BR1.1
ABSTRACT
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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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Doença de Chagas / Metalotioneína / Óxido Nítrico Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Mem. Inst. Oswaldo Cruz Assunto da revista: MEDICINA TROPICAL / PARASITOLOGIA Ano de publicação: 2014 Tipo de documento: Article / Project document País de afiliação: México País de publicação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Doença de Chagas / Metalotioneína / Óxido Nítrico Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Mem. Inst. Oswaldo Cruz Assunto da revista: MEDICINA TROPICAL / PARASITOLOGIA Ano de publicação: 2014 Tipo de documento: Article / Project document País de afiliação: México País de publicação: Brasil