Evidence map›Paper›PMID 32524267›Full record

ArticleParasitology research2020

Trichomonas vaginalis NTPDase inhibited by lycorine modulates the parasite-neutrophil interaction.

Brenda Petró-Silveira, Graziela Vargas Rigo, Danielle da Silva Trentin, Alexandre José Macedo, Elisa Sauer, Elen de Oliveira Alves, Luciana Ruschel Tallini, Solange Cristina Garcia, Warley de Souza Borges, José Ângelo Silveira Zuanazzi and 1 more

Abstract read
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In one paragraph

Article in Parasitology research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Infinity war:Microbial cell (Graz, Austria) · 2023
    Review
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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

11 authors at 3 institutions in 1 country.

Brenda Petró-SilveiraLaboratório de Pesquisa em Parasitologia, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Av. Ipiranga 2752, Porto Alegre, RS, 90610-000, Brazil.
Graziela Vargas RigoLaboratório de Pesquisa em Parasitologia, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Av. Ipiranga 2752, Porto Alegre, RS, 90610-000, Brazil.
Danielle da Silva TrentinDepartamento de Ciências Básicas da Saúde, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil.
Alexandre José MacedoLaboratório de Biofilmes e Diversidade Microbiana, Faculdade de Farmácia e Centro de Biotecnologia, Universidade do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Elisa SauerLaboratório de Toxicologia, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Elen de Oliveira AlvesLaboratório de Farmacognosia, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Luciana Ruschel TalliniLaboratório de Farmacognosia, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Solange Cristina GarciaLaboratório de Toxicologia, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Warley de Souza BorgesDepartamento de Química, Universidade Federal do Espírito Santo, Vitória, ES, Brazil.
José Ângelo Silveira ZuanazziLaboratório de Farmacognosia, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Tiana TascaLaboratório de Pesquisa em Parasitologia, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Av. Ipiranga 2752, Porto Alegre, RS, 90610-000, Brazil. tiana.tasca@ufrgs.br.ORCID http://orcid.org/0000-0002-8334-5105
Universidade Federal do Rio Grande do Sul · BRUniversidade Federal de Ciências da Saúde de Porto Alegre · BRUniversidade Federal do Espírito Santo · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303353/2016-3Conselho Nacional de Desenvolvimento Científico e Tecnológico 308052/17-0Conselho Nacional de Desenvolvimento Científico e Tecnológico 312292/2017-1Conselho Nacional de Desenvolvimento Científico e Tecnológico 428538/2018-5Conselho Nacional de Desenvolvimento Científico e Tecnológico 443150/2014-1Conselho Nacional de Desenvolvimento Científico e Tecnológico 465637/2014-0Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 13553135Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul 16/2551-0000244-4
6 · The paper itself

Abstract

Lycorine is an Amaryllidaceae alkaloid that presents anti-Trichomonas vaginalis activity. T. vaginalis causes trichomoniasis, the most common non-viral sexually transmitted infection. The modulation of T. vaginalis purinergic signaling through the ectonucleotidases, nucleoside triphosphate diphosphohydrolase (NTPDase), and ecto-5'-nucleotidase represents new targets for combating the parasite. With this knowledge, the aim of this study was to investigate whether NTPDase and ecto-5'-nucleotidase inhibition by lycorine could lead to extracellular ATP accumulation. Moreover, the lycorine effect on the reactive oxygen species (ROS) production by neutrophils and parasites was evaluated as well as the alkaloid toxicity. The metabolism of purines was assessed by HPLC. ROS production was measured by flow cytometry. Cytotoxicity against epithelial vaginal cells and fibroblasts was tested, as well as the hemolytic effect of lycorine and its in vivo toxicity in Galleria mellonella larvae. Our findings showed that lycorine caused ATP accumulation due to NTPDase inhibition. The alkaloid did not affect the ROS production by T. vaginalis; however, it increased ROS levels in neutrophils incubated with lycorine-treated trophozoites. Lycorine was cytotoxic against vaginal epithelial cells and fibroblasts; conversely, it was not hemolytic neither exhibited toxicity against the in vivo model of G. mellonella larvae. Overall, besides having anti-T. vaginalis activity, lycorine modulates ectonucleotidases and stimulates neutrophils to secrete ROS. This mechanism of action exerted by the alkaloid could enhance the susceptibility of T. vaginalis to host immune cell, contributing to protozoan clearance.

Indexed as

5'-NucleotidaseAmaryllidaceaeAmaryllidaceae AlkaloidsAntiprotozoal AgentsHumansNeutrophilsNucleoside-TriphosphatasePhenanthridinesPlant ExtractsProtozoan ProteinsReactive Oxygen SpeciesTrichomonas InfectionsTrichomonas vaginalisTrophozoites5'-NucleotidaseAmaryllidaceae AlkaloidsAntiprotozoal AgentslycorineNucleoside-TriphosphatasePhenanthridinesPlant ExtractsProtozoan ProteinsReactive Oxygen SpeciesAmaryllidaceaeGalleria mellonellaLycorineNTPDaseReactive oxygen speciesTrichomonas vaginalis

Identifiers

PMID32524267
OpenAlexW3033998474

What OpenQuestion holds

Textmetadata
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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.