MEM INST OSWALDO CRUZ, RIO DE JANEIRO, Vol. 112 | 2017
PAGES: DOI: 10.1590/0074-02760160499 Full paper
Dipyridamole potentiated the trypanocidal effect of nifurtimox and improved the cardiac function in NMRI mice with acute chagasic myocarditis

Sonia Santeliz1, Peter Caicedo2, Elidiosmar Giraldo2, Carmen Alvarez1, María-Daniela Yustiz2, Claudina Rodríguez-Bonfante3, Romina Bonfante-Rodríguez2, Rafael Bonfante-Cabarcas2,+

1Decanato de Ciencias Veterinarias, Unidad de Biomedicina, Departamento de Medicina y Cirugía, Barquisimeto, Estado Lara, Venezuela
2Decanato de Ciencias de la Salud, Unidad de Bioquímica, Barquisimeto, Estado Lara, Venezuela
3Universidad Centroccidental Lisandro Alvarado, Unidad de Parasitología Médica, Barquisimeto, Lara, Venezuela

Abstract

BACKGROUND As chronic Chagas disease does not have a definitive treatment, the development of alternative therapeutic protocols is a priority. Dipyridamole (DPY) is an alternative to counteract the pathophysiological phenomena involved in Chagas cardiomyopathy.

OBJECTIVE To evaluate the therapeutic efficacy of DPY associated with nifurtimox (Nfx) in epimastigote axenic cultures and in mice with acute Chagas disease.

METHODS NMRI adult male mice were divided into nine groups: three healthy and six Trypanosoma cruzi-infected groups. Mice received vehicle, Nfx or DPY, alone or combined. The doses assayed were Nfx 10 and 40 mg/kg and DPY 30 mg/kg. The treatment efficacy was evaluated by clinical, electrocardiographic, parasitological, biochemical and histopathological methods.

FINDINGS In vitro, DPY and Nfx had a trypanocidal effect with IC50 values of 372 ± 52 and 21.53 ± 2.13 μM, respectively; DPY potentiated the Nfx effect. In vivo, Nfx (40 mg/kg) with or without DPY had a therapeutic effect, which was reflected in the 84-92% survival rate and elimination of parasitaemia and heart tissue amastigotes. Nfx (10 mg/kg) had a subtherapeutic effect with no survival and persistence of amastigotes, inflammation and fibrosis in heart tissue; adding DPY increased the survival rate to 85%, and all tested parameters were significantly improved.

MAIN CONCLUSION DPY has a trypanocidal effect in vitro and enhances the Nfx therapeutic effect in an in vivo murine model.

Financial support: National Fund for Science and Technology (FONACIT) under the Ministry of Popular Power for Science and Technology (Venezuela) (Project No 2007001425) and by CDCHT at Universidad Centroccidental Lisandro Alvarado (Venezuela) (Doctoral project number 001-DVE-2014).
+ Corresponding author: This e-mail address is being protected from spambots. You need JavaScript enabled to view it.
Received 15 November 2016
Accepted 22 April 2017

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