Evidence map›Paper›PMID 33200281›Full record

ArticleClinical oral investigations2021

The use of host defense peptides in root canal therapy in rats.

Stella M F Lima, Mirna S Freire, Ana Paula C Cantuária, Danilo C M Martins, Ingrid A Amorim, Elaine M G L Dantas, Jade O Farias, Márcio B Castro, Jackson S Silva, Fernando A Barriviera and 9 more

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical oral investigations, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

19 authors at 7 institutions in 2 countries.

Stella M F LimaCurso de Odontologia, Universidade Católica de Brasília, Brasília, Distrito Federal, Brazil.
Mirna S FreireCentro de Análises Proteômicas e Bioquímicas, Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia, Universidade Católica de Brasília, SGAN 916N, Av. W5, Campus II, Modulo C, room C-221, Brasília, Distrito Federal, 70790-160, Brazil.
Ana Paula C CantuáriaCentro de Análises Proteômicas e Bioquímicas, Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia, Universidade Católica de Brasília, SGAN 916N, Av. W5, Campus II, Modulo C, room C-221, Brasília, Distrito Federal, 70790-160, Brazil.
Danilo C M MartinsCurso de Odontologia, Universidade Católica de Brasília, Brasília, Distrito Federal, Brazil.
Ingrid A AmorimCentro de Análises Proteômicas e Bioquímicas, Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia, Universidade Católica de Brasília, SGAN 916N, Av. W5, Campus II, Modulo C, room C-221, Brasília, Distrito Federal, 70790-160, Brazil.
Elaine M G L DantasCurso de Odontologia, Universidade Católica de Brasília, Brasília, Distrito Federal, Brazil.
Jade O FariasCurso de Odontologia, Universidade Católica de Brasília, Brasília, Distrito Federal, Brazil.
Márcio B CastroLaboratório de Patologia Veterinária, Universidade de Brasília, Brasília, Distrito Federal, Brazil.
Jackson S SilvaCurso de Odontologia, Centro Universitário do Distrito Federal, Brasília, Distrito Federal, Brazil.
Fernando A BarrivieraFenelon Radiologia, Brasília, Distrito Federal, Brazil.
Maurício BarrivieraFenelon Radiologia, Brasília, Distrito Federal, Brazil.
Jeeser A AlmeidaPrograma de Pós Graduação em Saúde e Desenvolvimento na Região Centro-Oeste, Universidade Federal de Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil.
Isadora A UeharaLaboratório de Biomarcadores Tumorais e Osteoimunologia, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.
Marcelo J B SilvaLaboratório de Biomarcadores Tumorais e Osteoimunologia, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.
Ana Paula L OliveiraFaculdade de Odontologia, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.
Osmar N SilvaS-Inova Biotech, Pós-Graduação em Biotecnologia, Universidade Católica Dom Bosco, Campo Grande, Mato Grosso do Sul, Brazil.
Robert E W HancockCentre for Microbial Diseases and Immunity Research, University of British Columbia, Vancouver, British Columbia, Canada.
Octávio L FrancoCentro de Análises Proteômicas e Bioquímicas, Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia, Universidade Católica de Brasília, SGAN 916N, Av. W5, Campus II, Modulo C, room C-221, Brasília, Distrito Federal, 70790-160, Brazil.
Taia M B RezendeCurso de Odontologia, Universidade Católica de Brasília, Brasília, Distrito Federal, Brazil. taiambr@gmail.com.ORCID http://orcid.org/0000-0002-4148-0659
Universidade de Brasília · BRUniversidade Católica de Brasília · BRUniversidade Federal de Uberlândia · BRCentro Universitário do Distrito Federal · BRUniversidade Católica Dom Bosco · BRUniversidade Federal de Mato Grosso do Sul · BRUniversity of British Columbia · CA

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 409196/2018-5Fundação de Apoio à Pesquisa do Distrito Federal (BR) 193.000.993/2015
6 · The paper itself

Abstract

objectivesIn order to evaluate host defense peptides (HDPs) HHC-10 and synoeca-MP activity in in vitro osteoclastogenesis process and in vivo induced apical periodontitis, testing the effect of molecules in the inflammatory response and in apical periodontitis size/volume after root canal treatment. MATERIALS AND

methodsIn vitro osteoclastogenesis was assessed on bone marrow cell cultures extracted from mice, while in vivo endodontic treatment involved rats treated with Ca(OH)

resultsNone of the substances downregulated the in vitro osteoclastogenesis. Nevertheless, all treatments affected the average of apical periodontitis size in rats, although only teeth treated with HDPs demonstrated lower levels of the inflammatory process. These results demonstrated the in vivo potential of HDPs. Radiographic analysis suggested that HHC-10 and synoeca-MP-treated animals presented a similar lesion size than Ca(OH)

conclusionsThese molecules demonstrated an auxiliary effect in endodontic treatment that might be related to its immunomodulatory ability, broad-spectrum antimicrobial activity, and possible induction of tissue repair at low concentrations. These results can encourage further investigations on the specific mechanisms of action in animal models to clarify the commercial applicability of these biomolecules for endodontic treatment. CLINICAL SIGNIFICANCE: HDPs have the potential to be adjuvant substances in endodontic therapy due to its potential to reduce inflammation in apical periodontitis.

Indexed as

Antimicrobial Cationic PeptidesPeriapical PeriodontitisAnimalsInflammationMiceRatsRoot Canal TherapyWound HealingAntimicrobial Cationic PeptidesAntimicrobial peptideApical periodontitisHHC-10Host defense peptidesSynoeca-MP

Identifiers

PMID33200281
OpenAlexW3100712334

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.