Evidence map›Paper›PMID 42478962›Full record

ArticleMemorias do Instituto Oswaldo Cruz2026

In vitro anti-Trypanosomatid activity and chemical profile of crude extracts of Chromolaena hookeriana and Campuloclinium macrocephalum (Asteraceae).

Ludmila Ferreira de Almeida Fiuza, Ketlym da Conceição, Krislayne Nunes, Aldana Malen Corlatti, Laura Cecilia Laurella, Simony Carvalho Mendonça, Brendo Araujo Gomes, Suzana Guimarães Leitão, Valeria Patricia Sülsen, Maria de Nazaré Correia Soeiro

Abstract read
In one paragraph

Article in Memorias do Instituto Oswaldo Cruz, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Phenotypic Analysis of the Anti-Molecules (Basel, Switzerland) · 2026
    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

10 authors.

Ludmila Ferreira de Almeida FiuzaFundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Biologia Celular, Rio de Janeiro, RJ, Brasil.
Ketlym da ConceiçãoFundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Biologia Celular, Rio de Janeiro, RJ, Brasil.
Krislayne NunesFundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Biologia Celular, Rio de Janeiro, RJ, Brasil.
Aldana Malen CorlattiConsejo Nacional de Investigaciones Científicas y Técnicas - Universidad de Buenos Aires, Instituto de Química y Metabolismo del Fármaco, Buenos Aires, Argentina.
Laura Cecilia LaurellaConsejo Nacional de Investigaciones Científicas y Técnicas - Universidad de Buenos Aires, Instituto de Química y Metabolismo del Fármaco, Buenos Aires, Argentina.
Simony Carvalho MendonçaUniversidade Federal do Rio de Janeiro, Faculdade de Farmácia, Departamento de Produtos Naturais e Alimentos, Rio de Janeiro, RJ, Brasil.
Brendo Araujo GomesUniversidade Federal do Rio de Janeiro, Faculdade de Farmácia, Departamento de Produtos Naturais e Alimentos, Rio de Janeiro, RJ, Brasil.
Suzana Guimarães LeitãoUniversidade Federal do Rio de Janeiro, Faculdade de Farmácia, Departamento de Produtos Naturais e Alimentos, Rio de Janeiro, RJ, Brasil.
Valeria Patricia SülsenConsejo Nacional de Investigaciones Científicas y Técnicas - Universidad de Buenos Aires, Instituto de Química y Metabolismo del Fármaco, Buenos Aires, Argentina.ORCID http://orcid.org/0000-0002-9322-5748
Maria de Nazaré Correia SoeiroFundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Biologia Celular, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0003-0078-6106

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChagas disease (CD) and Leishmaniasis, caused by Trypanosoma cruzi and Leishmania species, are treated with outdated drugs that are toxic and have limited efficacy. New therapeutic alternatives are therefore needed. Natural products are valuable scaffolds for drug discovery, and Asteraceae species exhibit microbicidal activity.

objectivesThis study evaluated the antiparasitic activity and selectivity of two Asteraceae species, Chromolaena hookeriana and Campuloclinium macrocephalum, against trypanosomatids.

methodsC. hookeriana and C. macrocephalum extracts were profiled by ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS), and their cytotoxicity and antiparasitic activity were evaluated against multiple forms and strains of T. cruzi and Leishmania amazonensis (L. amazonensis) in 2D and 3D cultures.

findingsUHPLC-MS/MS revealed predominantly pentacyclic triterpenoids in C. macrocephalum, including ursolic and oleanolic acids (negative mode) and lupeol derivatives (positive mode). C. macrocephalum was more effective than Benznidazole (Bz) (EC50 = 1.17 vs 4.47 µg/mL) against epimastigotes and nine times more potent against trypomastigotes (EC50 = 0.38 vs 3.5 µg/mL). Both extracts matched Bz activity on intracellular T. cruzi but exhibited time-dependent cytotoxicity. They also showed similar effectiveness to miltefosine (Mt) against L. amazonensis amastigotes (EC50 = 0.36-0.70 µg/mL). MAIN

conclusionsThe chemical profile supports the stronger antiparasitic activity of C. macrocephalum, likely linked to triterpenoids, and highlights Asteraceae extracts as promising candidates for drug discovery against neglected tropical diseases (NTDs).

Indexed as

AsteraceaeChromolaenaLeishmaniaPlant ExtractsTrypanocidal AgentsTrypanosoma cruziAnimalsChromatography, High Pressure LiquidParasitic Sensitivity TestsTandem Mass SpectrometryPlant ExtractsTrypanocidal Agents

Identifiers

PMID42478962
PMCPMC13183379

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.