Altered Cardiomyocyte Function and Trypanosoma cruzi Persistence in Chagas Disease

Author(s)

Cruz, Jader Santos ; Santos-Miranda, Artur ; Sales-Junior, Policarpo Ademar ; Monti-Rocha, Renata ; Campos, Paula Peixoto ; Machado, Fabiana Simao ; Roman-Campos, Danilo

• Document type: Journal article
• Source: American Journal of Tropical Medicine and Hygiene; v. 94, n. 5, p. 1028-1033, 2016.
• Web of Science Citations: 5

Abstract

Chagas disease, caused by the triatominae Trypanosoma cruzi, is one of the leading causes of heart malfunctioning in Latin America. The cardiac phenotype is observed in 20-30% of infected people 10-40 years after their primary infection. The cardiac complications during Chagas disease range from cardiac arrhythmias to heart failure, with important involvement of the right ventricle. Interestingly, no studies have evaluated the electrical properties of right ventricle myocytes during Chagas disease and correlated them to parasite persistence. Taking advantage of a murine model of Chagas disease, we studied the histological and electrical properties of right ventricle in acute (30 days postinfection {[}dpi]) and chronic phases (90 dpi) of infected mice with the Colombian strain of T. cruzi and their correlation to parasite persistence. We observed an increase in collagen deposition and inflammatory infiltrate at both 30 and 90 dpi. Furthermore, using reverse transcriptase polymerase chain reaction, we detected parasites at 90 dpi in right and left ventricles. In addition, we observed action potential prolongation and reduced transient outward K+ current and L-type Ca2+ current at 30 and 90 dpi. Taking together, our results demonstrate that T. cruzi infection leads to important modifications in electrical properties associated with inflammatory infiltrate and parasite persistence in mice right ventricle, suggesting a causal role between inflammation, parasite persistence, and altered cardiomyocyte function in Chagas disease. Thus, arrhythmias observed in Chagas disease may be partially related to altered electrical function in right ventricle. (AU)

• FAPESP's process: 14/09861-1 - The role of late sodium current in the inherited and acquired cardiac arrhythmias: from the biophysics properties to new therapeutic targets
• Grantee: Danilo Roman Campos
• Support Opportunities: Research Grants - Young Investigators Grants