Early dystrophin disruption in the pathogenesis of experimental chronic Chagas cardiomyopathy
dc.creator | Prado, Cibele Maria | |
dc.creator | Celes, Mara Rúbia Nunes | |
dc.creator | Giancotti, Lygia Maria Malvestio | |
dc.creator | Pulici, Erica Carolina Campos | |
dc.creator | Silva, João Santana da | |
dc.creator | Jelicks, Linda A. | |
dc.creator | Tanowitz, Herbert B. | |
dc.creator | Rossi, Marcos Antonio | |
dc.date.accessioned | 2025-02-10T13:26:45Z | |
dc.date.available | 2025-02-10T13:26:45Z | |
dc.date.issued | 2012 | |
dc.description.abstract | Chronic Chagas cardiomyopathy evolves over a long period of time after initial infection by Trypanosoma cruzi. Similarly, a cardiomyopathy appears later in life in muscular dystrophies. This study tested the hypothesis that dystrophin levels are decreased in the early stage of T. cruzi infected mice that precedes the later development of a cardiomyopathy. CD1 mice were infected with T. cruzi (Brazil strain), killed at 30 and 100 days post infection (dpi), and the intensity of inflammation, percentage of interstitial fibrosis, and dystrophin levels evaluated. Echocardiography and magnetic resonance imaging data were evaluated from 15 to 100 dpi. At 30 dpi an intense acute myocarditis with ruptured or intact intracellular parasite nests was observed. At 100 dpi a mild chronic fibrosing myocarditis was detected without parasites in the myocardium. Dystrophin was focally reduced or completely lost in cardiomyocytes at 30 dpi, with the reduction maintained up to 100 dpi. Concurrently, ejection fraction was reduced and the right ventricle was dilated. These findings support the hypothesis that the initial parasitic infection-induced myocardial dystrophin reduction/loss, maintained over time, might be essential to the late development of a cardiomyopathy in mice. 2011 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved. | |
dc.identifier.citation | PRADO, Cibele M. et al. Early dystrophin disruption in the pathogenesis of experimental chronic Chagas cardiomyopathy. Microbes and Infection, Paris, v. 14, n. 1, p. 59-68, 2012. DOI: 10.1016/j.micinf.2011.08.010. Disponível em: https://linkinghub.elsevier.com/retrieve/pii/S1286-4579(11)00223-1. Acesso em: 7 fev. 2025. | |
dc.identifier.doi | 10.1016/j.micinf.2011.08.010 | |
dc.identifier.issn | 1286-4579 | |
dc.identifier.issn | e- 1769-714X | |
dc.identifier.uri | http://repositorio.bc.ufg.br//handle/ri/26635 | |
dc.language.iso | eng | |
dc.publisher.country | Franca | |
dc.publisher.department | Instituto de Patologia Tropical e Saúde Pública - IPTSP (RMG) | |
dc.rights | Acesso Aberto | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Chronic Chagas cardiomyopathy | |
dc.subject | Dystrophin | |
dc.subject | Chagas disease | |
dc.subject | Dystrophinopathy | |
dc.subject | Trypanosoma cruzi | |
dc.title | Early dystrophin disruption in the pathogenesis of experimental chronic Chagas cardiomyopathy | |
dc.type | Artigo |
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