Efficacy of the benznidazole+posaconazole combination therapy in parasitemia reduction: An experimental murine model of acute chagas

Introduction: Benznidazole (BZL) and Nifurtimox (NFX) are the pharmacological treatment for acute phase Chagas Disease (CD); however, therapy resistance and residual mortality development remain important unresolved issues. Posaconazole (POS) has shown a trypanocidal effect in vivo and in vitro. Thu...

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Autores:
Echeverría L.E.
González C.I.
Hernandez J.C.M.
Díaz M.L.
Nieto Pico, Javier eduardo
López-Romero L.A.
Rivera J.D.
Suárez E.U.
Ochoa S.A.G.
Rojas L.Z.
Morillo C.A.
Tipo de recurso:
Article of journal
Fecha de publicación:
2023
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/51041
Acceso en línea:
https://doi.org/10.1590/0037-8682-0477-2019
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85079336125&doi=10.1590%2f0037-8682-0477-2019&partnerID=40&md5=d6edadee009fccda59130dc0f635b86b
https://hdl.handle.net/20.500.12494/51041
Palabra clave:
BENZNIDAZOLE AND POSACONAZOLE
CHAGAS DISEASE
TRYPANOCIDAL
WISTAR RATS
Rights
openAccess
License
http://purl.org/coar/access_right/c_abf2
Description
Summary:Introduction: Benznidazole (BZL) and Nifurtimox (NFX) are the pharmacological treatment for acute phase Chagas Disease (CD); however, therapy resistance and residual mortality development remain important unresolved issues. Posaconazole (POS) has shown a trypanocidal effect in vivo and in vitro. Thus, this study aimed at comparing the T. Cruzi parasitic load-reducing effect of the combination of BZL+POS against that of monotherapy with either, during acute phase CD, in an experimental murine model. Methods: Nineteen Wistar rats were randomly allocated to four groups and inoculated with the trypomastigotes of T. cruzi strain´s JChVcl1. The rats were administered anti-parasites from day 20-29 post-infection. The Pizzi and Brener method was used for parasitemia measurement. Longitudinal data analysis for the continuous outcome of repeated measures was performed using parasitemia as the outcome measured at days 20, 22, 24, 27, and 29 post-infection. Results: All four groups had similar parasitic loads (p=0.143) prior to therapy initiation. Among the three treatment groups, the BZL+POS (n=5) group showed the highest mean parasitic load reduction (p=0.000) compared with the control group. Likewise, the BZL+POS group rats showed an earlier therapeutic effect and were the only ones without parasites in their myocardial samples. Conclusions: Treatment of acute phase CD with BZL+POS was more efficacious at parasitemia and myocardial injury reduction, compared with monotherapy with either. © 2020, Sociedade Brasileira de Medicina Tropical. All rights reserved.