Evidence map›Paper›PMID 39509468›Full record

ArticlePLoS neglected tropical diseases2024

Heart function enhancement by an Nrf2-activating antioxidant in acute Y-strain Chagas disease, but not in chronic Colombian or Y-strain.

Hilton Antônio Mata-Santos, Camila Victória Sousa Oliveira, Daniel F Feijo, Daniel Figueiredo Vanzan, Glaucia Vilar-Pereira, Isalira P Ramos, Vitor Coutinho Carneiro, Oscar Moreno-Loaiza, Jaline Coutinho Silverio, Joseli Lannes-Vieira and 3 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. 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. Article
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

13 authors.

Hilton Antônio Mata-SantosFaculdade de Farmácia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
Camila Victória Sousa OliveiraInstituto de Microbiologia Paulo de Goes, UFRJ, Rio de Janeiro, Brazil.
Daniel F FeijoInstituto de Microbiologia Paulo de Goes, UFRJ, Rio de Janeiro, Brazil.
Daniel Figueiredo VanzanFaculdade de Farmácia, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
Glaucia Vilar-PereiraOswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Isalira P RamosCentro Nacional de Biologia Estrutural e Bioimagem, UFRJ, Rio de Janeiro, Brazil.
Vitor Coutinho CarneiroInstituto de Bioquímica, UFRJ, Rio de Janeiro, Brazil.
Oscar Moreno-LoaizaInstitute of Biophysics Carlos Chagas Filho, UFRJ, Rio de Janeiro, Brazil.
Jaline Coutinho SilverioOswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Joseli Lannes-VieiraOswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Emiliano MedeiInstitute of Biophysics Carlos Chagas Filho, UFRJ, Rio de Janeiro, Brazil.
Marcelo T BozzaInstituto de Microbiologia Paulo de Goes, UFRJ, Rio de Janeiro, Brazil.
Claudia N PaivaInstituto de Microbiologia Paulo de Goes, UFRJ, Rio de Janeiro, Brazil.ORCID 0000-0001-5605-3572

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Brasil (CAPES)Instituto de Microbiologia Paulo de Góes/UFRJ
6 · The paper itself

Abstract

Oxidative stress promotes T. cruzi growth and development of chronic Chagas heart dysfunction. However, the literature contains gaps that must be fulfilled, largely due to variations in parasite DTU sources, cell types, mouse strains, and tools to manipulate redox status. We assessed the impact of oxidative environment on parasite burden in cardiomyoblasts and the effects of the Nrf2-inducer COPP on heart function in BALB/c mice infected with either DTU-II Y or DTU-I Colombian T. cruzi strains. Treatment with antioxidants CoPP, apocynin, resveratrol, and tempol reduced parasite burden in cardiomyoblasts H9C2 for both DTUI- and II-strains, while H2O2 increased it. CoPP treatment improved electrical heart function when administered during acute stage of Y-strain infection, coinciding with an overall trend towards increased survival and reduced heart parasite burden. These beneficial effects surpassed those of trypanocidal benznidazole, implying that CoPP directly affects heart physiology. CoPP treatment had beneficial impact on heart systolic function when performed during acute and evaluated during chronic stage. No impact of CoPP on heart parasite burden, electrical, or mechanical function was observed during the chronic stage of Colombian-strain infection, despite previous demonstrations of improvement with other antioxidants. Treatment with CoPP also did not improve heart function of mice chronically infected with Y-strain. Our findings indicate that amastigote growth is responsive to changes in oxidative environment within heart cells regardless of the DTU source, but CoPP influence on heart parasite burden in vivo and heart function is mostly confined to the acute phase. The nature of the antioxidant employed, T. cruzi DTU, and the stage of disease, emerge as crucial factors to consider in heart function studies.

Indexed as

AntioxidantsChagas DiseaseMice, Inbred BALB CNF-E2-Related Factor 2Oxidative StressTrypanosoma cruziAnimalsChagas CardiomyopathyChronic DiseaseColombiaDisease Models, AnimalFemaleHeartMaleMiceParasite LoadAntioxidantsNfe2l2 protein, mouseNF-E2-Related Factor 2

Identifiers

PMID39509468
PMCPMC11588235

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.