Evidence map›Paper›PMID 36884141›Full record

ArticleActa parasitologica2023

Zinc and Manganese Imbalances in BALB/c Mice Experimentally Infected with Leishmania (Leishmania) amazonensis.

Caroline Sobotyk, Fernanda Giesel Baldissera, Luiz Carlos Rodrigues Junior, Pedro Roosevelt Torres Romão, Juliana Sorraila de Oliveira, Guilherme Lopes Dornelles, Cinthia Melazzo de Andrade, Roberto Marinho Maciel, Cristiane Cademartori Danesi, Rafael Vicente de Padua Ferreira and 4 more

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Article in Acta parasitologica, 2023. 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
0.6field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  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

14 authors at 3 institutions in 2 countries.

Caroline SobotykDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA. csobotyk@vet.upenn.edu.ORCID http://orcid.org/0000-0002-3986-6018
Fernanda Giesel BaldisseraDepartamento de Ciências Básicas da Saúde, Universidade Federal de Ciências da Saúde de Porto Alegre, Rua Sarmento Leite, 245, Porto Alegre, RS, 90050-170, Brazil.
Luiz Carlos Rodrigues JuniorDepartamento de Ciências Básicas da Saúde, Universidade Federal de Ciências da Saúde de Porto Alegre, Rua Sarmento Leite, 245, Porto Alegre, RS, 90050-170, Brazil.
Pedro Roosevelt Torres RomãoDepartamento de Ciências Básicas da Saúde, Universidade Federal de Ciências da Saúde de Porto Alegre, Rua Sarmento Leite, 245, Porto Alegre, RS, 90050-170, Brazil.
Juliana Sorraila de OliveiraPrograma de Pós-graduação em Medicina Veterinária (PPGMV), Departamento de Clínica de Pequenos Animais, Universidade Federal de Santa (UFSM), Av. Roraima, 1000, Camobi, Santa Maria, RS, 97105900, Brazil.
Guilherme Lopes DornellesPrograma de Pós-graduação em Medicina Veterinária (PPGMV), Departamento de Clínica de Pequenos Animais, Universidade Federal de Santa (UFSM), Av. Roraima, 1000, Camobi, Santa Maria, RS, 97105900, Brazil.
Cinthia Melazzo de AndradePrograma de Pós-graduação em Medicina Veterinária (PPGMV), Departamento de Clínica de Pequenos Animais, Universidade Federal de Santa (UFSM), Av. Roraima, 1000, Camobi, Santa Maria, RS, 97105900, Brazil.
Roberto Marinho MacielDepartamento de Patologia, UFSM, Av. Roraima, 1000, Camobi, Santa Maria, RS, 97105900, Brazil.
Cristiane Cademartori DanesiDepartamento de Patologia, UFSM, Av. Roraima, 1000, Camobi, Santa Maria, RS, 97105900, Brazil.
Rafael Vicente de Padua FerreiraLaboratório de Biologia Celular e Molecular do Câncer, Centro de Biotecnologia, Instituto de Pesquisas Energéticas e Nucleares, Av. Professor Lineu Prestes, 2242, Cidade Universitária, Butantã, São Paulo, SP, 05508-000, Brazil.
Maria Helena BelliniLaboratório de Biologia Celular e Molecular do Câncer, Centro de Biotecnologia, Instituto de Pesquisas Energéticas e Nucleares, Av. Professor Lineu Prestes, 2242, Cidade Universitária, Butantã, São Paulo, SP, 05508-000, Brazil.
Sônia de Avila BottonDepartamento de Medicina Veterinária Preventiva, PPGMV, UFSM, Av. Roraima, 1000, Camobi, Santa Maria, RS, 97105900, Brazil.
Fernanda Silveira Flores VogelDepartamento de Medicina Veterinária Preventiva, PPGMV, UFSM, Av. Roraima, 1000, Camobi, Santa Maria, RS, 97105900, Brazil.
Luis Antonio SangioniDepartamento de Medicina Veterinária Preventiva, PPGMV, UFSM, Av. Roraima, 1000, Camobi, Santa Maria, RS, 97105900, Brazil.
Universidade Federal de Santa Maria · BRUniversidade Federal de Ciências da Saúde de Porto Alegre · BRInstituto de Pesquisas Energéticas e Nucleares · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico Finance Code 001Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Finance Code 001
6 · The paper itself

Abstract

purposeThe clinical progression of Leishmania (Leishmania) amazonensis infection depends on multiple factors, including immunological status of the host and their genotypic interaction. Several immunological processes depend directly on minerals for an efficient performance. Therefore, this study used an experimental model to investigate the alterations of trace metals in L. amazonensis infection associate with clinical outcome, parasite load, and histopathological lesions, and the effect of CD4 + T cells depletion on these parameters.

methodsA total of 28 BALB/c mice were divided into 4 groups: 1-non-infected; 2-treated with anti-CD4 antibody; 3-infected with L. amazonensis; and 4-treated with anti-CD4 antibody and infected with L. amazonensis. After 24 weeks post-infection, levels of calcium (Ca), iron (Fe), magnesium (Mg), manganese (Mn), Cu, and Zn were determined by inductively coupled plasma optical emission spectroscopy using tissue samples of the spleen, liver, and kidneys. Additionally, parasite burdens were determined in the infected footpad (inoculation site) and samples of inguinal lymph node, spleen, liver, and kidneys were submitted to histopathological analysis.

resultsDespite no significant difference was observed between groups 3 and 4, L. amazonensis-infected mice had a significant reduction of Zn (65.68-68.32%) and Mn (65.98 to 82.17%) levels. Presence of L. amazonensis amastigotes was also detected in the inguinal lymph node, spleen, and liver samples in all infected animals.

conclusionThe results showed that significant alterations in micro-elements levels occur in BALB/c mice experimentally infected with L. amazonensis and may increase the susceptibility of individuals to the infection.

Indexed as

LeishmaniaLeishmaniasis, CutaneousAnimalsManganeseMiceMice, Inbred BALB CZincManganeseZincCD4 + T cellsCutaneous leishmaniasisLeishmania sp.MicroelementsTrace elements

Identifiers

PMID36884141
OpenAlexW4323535554

What OpenQuestion holds

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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 OpenQuestion graph.