Evidence map›Paper›PMID 40488037›Full record

ArticleACS omega2025

Amiodarone and Ravuconazole Combination Potentiates Chemotherapy against Drug-Resistant Trypanosoma cruzi Strains.

Breno Vilas Boas Raimundo, Ana Lia Mazzeti, Maria Terezinha Bahia, Ivo Santana Caldas, Valquíria Ângelis Fernandes, Elda Gonçalves Santos, Rodrigo Dian de Oliveira Aguiar Soares, Aline Silva de Miranda, Rômulo Dias Novaes, Lívia de Figueiredo Diniz

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Breno Vilas Boas RaimundoLaboratório de Parasitologia Básica, Departamento de Patologia e Parasitologia, Instituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas 37130-000, Minas Gerais, Brazil.
Ana Lia MazzetiLaboratório de Parasitologia Básica e Aplicada, Departamento de Ciências Biomédicas e Saúde, Universidade do Estado de Minas Gerais, Passos 37900-106, Minas Gerais, Brazil.
Maria Terezinha BahiaNúcleo de Pesquisas em Ciências Biológicas, Universidade Federal de Ouro Preto, Ouro Preto 35400-000, Minas Gerais, Brazil.
Ivo Santana CaldasLaboratório de Parasitologia Básica, Departamento de Patologia e Parasitologia, Instituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas 37130-000, Minas Gerais, Brazil.
Valquíria Ângelis FernandesLaboratório de Parasitologia Básica, Departamento de Patologia e Parasitologia, Instituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas 37130-000, Minas Gerais, Brazil.
Elda Gonçalves SantosDepartamento de Biologia Estrutural, Instituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas 37130-000, Minas Gerais, Brazil.
Rodrigo Dian de Oliveira Aguiar SoaresNúcleo de Pesquisas em Ciências Biológicas, Universidade Federal de Ouro Preto, Ouro Preto 35400-000, Minas Gerais, Brazil.
Aline Silva de MirandaLaboratório de Neurobiologia "Conceição Machado", Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil.
Rômulo Dias NovaesDepartamento de Biologia Estrutural, Instituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas 37130-000, Minas Gerais, Brazil.
Lívia de Figueiredo DinizLaboratório de Parasitologia Básica, Departamento de Patologia e Parasitologia, Instituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas 37130-000, Minas Gerais, Brazil.ORCID https://orcid.org/0000-0001-9398-6478

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug combinations represent valuable opportunities for developing more effective and safer treatments for Chagas disease. In this study, we investigated the effects of ravuconazole and amiodarone combinations against Trypanosoma cruzi infection. After ruling out antagonistic effects and increased cytotoxicity in vitro, a short-term in vivo protocol was used to evaluate parasitemia, immune response, and heart damage caused by the Y and Colombian T. cruzi strains in BALB/c and Swiss mice. Untreated mice displayed elevated parasitemia and pro-inflammatory cytokine levels, with strain-specific differences in IL-10 levels and the presence of parasites in the myocardium. Amiodarone monotherapy failed to exhibit in vivo anti-T. cruzi activity. While ravuconazole monotherapy at a subtherapeutic dose reduced parasitemia in all treated animals, its effects on the host response varied depending on the mouse and parasite strain, demonstrating greater activity in Swiss mice infected with the Y strain. Remarkably, amiodarone enhanced ravuconazole efficacy as combination chemotherapy was more effective than monotherapy in downregulating parasite load and pro-inflammatory cytokine levels, attenuating cardiac damage in all experimental models. These findings demonstrate a positive in vivo interaction between ravuconazole and amiodarone against T. cruzi infection. Furthermore, they highlight the relevance of the host genetic background and parasite strain on treatment outcomes.

Identifiers

PMID40488037
PMCPMC12138704

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.