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Experimental Combination Therapy with Amiodarone and Low-Dose Benznidazole in a Mouse Model of Trypanosoma cruzi Acute Infection

Chagas disease (CD), caused by Trypanosoma cruzi, affects approximately 6 to 7 million people in Latin America, with cardiomyopathy being the clinical manifestation most commonly associated with patient death during the acute phase. The etiological treatment of CD is restricted to benznidazole (Bz)...

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Autores principales: Barbosa, Juliana Magalhães Chaves, Pedra Rezende, Yasmin, de Melo, Tatiana Galvão, de Oliveira, Gabriel, Cascabulho, Cynthia Machado, Pereira, Evelyn Nunes Goulart da Silva, Daliry, Anissa, Salem, Kelly Salomão
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826820/
https://www.ncbi.nlm.nih.gov/pubmed/35138142
http://dx.doi.org/10.1128/spectrum.01852-21
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author Barbosa, Juliana Magalhães Chaves
Pedra Rezende, Yasmin
de Melo, Tatiana Galvão
de Oliveira, Gabriel
Cascabulho, Cynthia Machado
Pereira, Evelyn Nunes Goulart da Silva
Daliry, Anissa
Salem, Kelly Salomão
author_facet Barbosa, Juliana Magalhães Chaves
Pedra Rezende, Yasmin
de Melo, Tatiana Galvão
de Oliveira, Gabriel
Cascabulho, Cynthia Machado
Pereira, Evelyn Nunes Goulart da Silva
Daliry, Anissa
Salem, Kelly Salomão
author_sort Barbosa, Juliana Magalhães Chaves
collection PubMed
description Chagas disease (CD), caused by Trypanosoma cruzi, affects approximately 6 to 7 million people in Latin America, with cardiomyopathy being the clinical manifestation most commonly associated with patient death during the acute phase. The etiological treatment of CD is restricted to benznidazole (Bz) and nifurtimox (Nif), which involve long periods of administration, frequent side effects, and low efficacy in the chronic phase. Thus, combined therapies emerge as an important tool in the treatment of CD, allowing the reduction of Bz dose and treatment duration. In this sense, amiodarone (AMD), the most efficient antiarrhythmic drug currently available and prescribed to CD patients, is a potential candidate for combined treatment due to its known trypanocidal activity. However, the efficacy of AMD during the acute phase of CD and its interaction with Bz or Nif are still unknown. In the present study, using a well-established murine model of the acute phase of CD, we observed that the Bz/AMD combination was more effective in reducing the peak parasitemia than both monotherapy treatments. Additionally, the Bz/AMD combination reduced (i) interleukin-6 (IL-6) levels in cardiac tissue, (ii) P-wave duration, and (iii) frequency of arrhythmia in infected animals and (iv) restored gap junction integrity in cardiac tissue. Therefore, our study validates AMD as a promising candidate for combined therapy with Bz, reinforcing the strategy of combined therapy for CD. IMPORTANCE Chagas disease affects approximately 6 to 7 million people worldwide, with cardiomyopathy being the clinical manifestation that most commonly leads to patient death. The etiological treatment of Chagas disease is limited to drugs (benznidazole and nifurtimox) with relatively high toxicity and therapeutic failures. In this sense, amiodarone, the most effective currently available antiarrhythmic drug prescribed to patients with Chagas disease, is a potential candidate for combined treatment due to its known trypanocidal effect. In the present study, we show that combined treatment with benznidazole and amiodarone improves the trypanocidal effect and reduces cardiac damage in acutely T. cruzi-infected mice.
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spelling pubmed-88268202022-02-17 Experimental Combination Therapy with Amiodarone and Low-Dose Benznidazole in a Mouse Model of Trypanosoma cruzi Acute Infection Barbosa, Juliana Magalhães Chaves Pedra Rezende, Yasmin de Melo, Tatiana Galvão de Oliveira, Gabriel Cascabulho, Cynthia Machado Pereira, Evelyn Nunes Goulart da Silva Daliry, Anissa Salem, Kelly Salomão Microbiol Spectr Research Article Chagas disease (CD), caused by Trypanosoma cruzi, affects approximately 6 to 7 million people in Latin America, with cardiomyopathy being the clinical manifestation most commonly associated with patient death during the acute phase. The etiological treatment of CD is restricted to benznidazole (Bz) and nifurtimox (Nif), which involve long periods of administration, frequent side effects, and low efficacy in the chronic phase. Thus, combined therapies emerge as an important tool in the treatment of CD, allowing the reduction of Bz dose and treatment duration. In this sense, amiodarone (AMD), the most efficient antiarrhythmic drug currently available and prescribed to CD patients, is a potential candidate for combined treatment due to its known trypanocidal activity. However, the efficacy of AMD during the acute phase of CD and its interaction with Bz or Nif are still unknown. In the present study, using a well-established murine model of the acute phase of CD, we observed that the Bz/AMD combination was more effective in reducing the peak parasitemia than both monotherapy treatments. Additionally, the Bz/AMD combination reduced (i) interleukin-6 (IL-6) levels in cardiac tissue, (ii) P-wave duration, and (iii) frequency of arrhythmia in infected animals and (iv) restored gap junction integrity in cardiac tissue. Therefore, our study validates AMD as a promising candidate for combined therapy with Bz, reinforcing the strategy of combined therapy for CD. IMPORTANCE Chagas disease affects approximately 6 to 7 million people worldwide, with cardiomyopathy being the clinical manifestation that most commonly leads to patient death. The etiological treatment of Chagas disease is limited to drugs (benznidazole and nifurtimox) with relatively high toxicity and therapeutic failures. In this sense, amiodarone, the most effective currently available antiarrhythmic drug prescribed to patients with Chagas disease, is a potential candidate for combined treatment due to its known trypanocidal effect. In the present study, we show that combined treatment with benznidazole and amiodarone improves the trypanocidal effect and reduces cardiac damage in acutely T. cruzi-infected mice. American Society for Microbiology 2022-02-09 /pmc/articles/PMC8826820/ /pubmed/35138142 http://dx.doi.org/10.1128/spectrum.01852-21 Text en Copyright © 2022 Barbosa et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Barbosa, Juliana Magalhães Chaves
Pedra Rezende, Yasmin
de Melo, Tatiana Galvão
de Oliveira, Gabriel
Cascabulho, Cynthia Machado
Pereira, Evelyn Nunes Goulart da Silva
Daliry, Anissa
Salem, Kelly Salomão
Experimental Combination Therapy with Amiodarone and Low-Dose Benznidazole in a Mouse Model of Trypanosoma cruzi Acute Infection
title Experimental Combination Therapy with Amiodarone and Low-Dose Benznidazole in a Mouse Model of Trypanosoma cruzi Acute Infection
title_full Experimental Combination Therapy with Amiodarone and Low-Dose Benznidazole in a Mouse Model of Trypanosoma cruzi Acute Infection
title_fullStr Experimental Combination Therapy with Amiodarone and Low-Dose Benznidazole in a Mouse Model of Trypanosoma cruzi Acute Infection
title_full_unstemmed Experimental Combination Therapy with Amiodarone and Low-Dose Benznidazole in a Mouse Model of Trypanosoma cruzi Acute Infection
title_short Experimental Combination Therapy with Amiodarone and Low-Dose Benznidazole in a Mouse Model of Trypanosoma cruzi Acute Infection
title_sort experimental combination therapy with amiodarone and low-dose benznidazole in a mouse model of trypanosoma cruzi acute infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826820/
https://www.ncbi.nlm.nih.gov/pubmed/35138142
http://dx.doi.org/10.1128/spectrum.01852-21
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