Evidence map›Paper›PMID 35190878›Full record

SynthesisParasitology research2022

The anti-Leishmania potential of bioactive compounds derived from naphthoquinones and their possible applications. A systematic review of animal studies.

Áquila Carolina Fernandes Herculano Ramos-Milaré, Jully Oyama, Letícia Sayuri Murase, João Vítor Perez Souza, Bárbara Silva Guedes, Daniele Stéfanie Sara Lopes Lera-Nonose, Mariana Terron Monich, Aline Ávila Brustolin, Izabel Galhardo Demarchi, Jorge Juarez Vieira Teixeira and 1 more

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Parasitology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Reaction Mechanisms of HAntioxidants (Basel, Switzerland) · 2024
    Article
  4. Article
  5. 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

11 authors at 2 institutions in 1 country.

Áquila Carolina Fernandes Herculano Ramos-MilaréGraduate Program in Health Sciences, State University of Maringá, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil. aquilacarolina.fhr@gmail.com.ORCID http://orcid.org/0000-0001-9068-7958
Jully OyamaGraduate Program in Biosciences and Physiopathology, State University of Maringa, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
Letícia Sayuri MuraseGraduate Program in Health Sciences, State University of Maringá, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
João Vítor Perez SouzaGraduate Program in Biosciences and Physiopathology, State University of Maringa, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
Bárbara Silva GuedesGraduate Program in Biosciences and Physiopathology, State University of Maringa, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
Daniele Stéfanie Sara Lopes Lera-NonoseGraduate Program in Health Sciences, State University of Maringá, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
Mariana Terron MonichGraduate Program in Health Sciences, State University of Maringá, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
Aline Ávila BrustolinGraduate Program in Health Sciences, State University of Maringá, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
Izabel Galhardo DemarchiDepartment of Clinical Analysis, Federal University of Santa Catarina, Trindade-Florianópolis, Santa Catarina, 88040-900, Brazil.
Jorge Juarez Vieira TeixeiraDepartment of Clinical Analysis and Biomedicine, State University of Maringa, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
Maria Valdrinez Campana LonardoniDepartment of Clinical Analysis and Biomedicine, State University of Maringa, Colombo Avenue, 5790, Maringá, Paraná, 87020-900, Brazil.
Universidade Estadual de Maringá · BRUniversidade Federal de Santa Catarina · BR

Funding

coordenação de aperfeiçoamento de pessoal de nível superior Finance code 001
6 · The paper itself

Abstract

Leishmaniasis affects millions of people worldwide, and available treatments have severe limitations. Natural and derivative products are significant sources of innovative therapeutic agents. Naphthoquinones are natural or synthetic chemical compounds with broad biological activity. This systematic review aimed to evaluate the potential anti-Leishmania activity of bioactive compounds derived from naphthoquinones in animal models. Conducted in accordance with PRISMA guidelines, two blocks of MeSH terms were assembled: group I, Leishmania OR Leishmaniasis; group II, Atovaquone OR Lapachol OR Beta lapachone OR Naphthoquinones. The search was performed on PubMed, Web of Science, SCOPUS, EMBASE, and Lilacs databases. Twenty-four articles were retrieved and submitted for quality assessment using the SYRCLE critical appraisal tool. The in vivo anti-Leishmania potential of naphthoquinones was evaluated in visceral and cutaneous leishmaniasis using several measurement parameters. Analyzed compounds varied in structure, association with reference drugs, and encapsulation using a drug delivery system. The study design, including treatment protocol, differed between studies. The findings of the studies in this systematic review indicate the anti-Leishmania potential of naphthoquinones in vivo, with different treatment regimens directed against different Leishmania species. The employed drug delivery systems improve the results concerning selectivity, distribution, and required therapeutic dose. The immunomodulatory action was shown to be beneficial to the host, favoring an adequate immune response against infection by Leishmania parasites since it favored Th

Indexed as

Antiprotozoal AgentsLeishmaniaLeishmaniasis, CutaneousNaphthoquinonesAnimalsAnimals, LaboratoryHumansAntiprotozoal AgentsNaphthoquinonesAntileishmanial activityCutaneous leishmaniasisDrug deliveryLeishmaniasisNaphthoquinonesVisceral leishmaniasis

Identifiers

PMID35190878
OpenAlexW4213181860

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.