Evidence map›Paper›PMID 28825161›Full record

ArticleInflammopharmacology2018

Anti-inflammatory effect of a new piperazine derivative: (4-methylpiperazin-1-yl)(1-phenyl-1H-pyrazol-4-yl)methanone.

Daniel C Batista, Daiany P B Silva, Iziara F Florentino, Carina S Cardoso, Merita P Gonçalves, Marize C Valadares, Luciano M Lião, Germán Sanz, Boniek G Vaz, Elson A Costa and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammopharmacology, 2018. 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
0.9field-weighted citation impact, top 25% 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, 20 citations in OpenAlex.

  1. Article
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  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 1 institution in 1 country.

Daniel C BatistaFaculty of Pharmacy, Laboratory of Medicinal Pharmaceutical Chemistry, Federal University of Goiás, Goiânia, GO, Brazil.
Daiany P B SilvaDepartment of Pharmacology, ICB, Federal University of Goiás, Campus Samambaia, 314, Goiânia, GO, 74001-970, Brazil.
Iziara F FlorentinoDepartment of Pharmacology, ICB, Federal University of Goiás, Campus Samambaia, 314, Goiânia, GO, 74001-970, Brazil.
Carina S CardosoDepartment of Pharmacology, ICB, Federal University of Goiás, Campus Samambaia, 314, Goiânia, GO, 74001-970, Brazil.
Merita P GonçalvesDepartment of Pharmacology, ICB, Federal University of Goiás, Campus Samambaia, 314, Goiânia, GO, 74001-970, Brazil.
Marize C ValadaresLaboratory of Pharmacology and Cell Toxicology, Faculty of Pharmacy, Federal University of Goiás, Goiânia, GO, Brazil.
Luciano M LiãoChemistry Institute, Federal University of Goias, Campus Samambaia, Goiânia, GO, Brazil.
Germán SanzChemistry Institute, Laboratory of Chromatography and Mass Spectrometry-LaCEM, Federal University of Goiás, Goiânia, GO, Brazil.
Boniek G VazChemistry Institute, Laboratory of Chromatography and Mass Spectrometry-LaCEM, Federal University of Goiás, Goiânia, GO, Brazil.
Elson A CostaDepartment of Pharmacology, ICB, Federal University of Goiás, Campus Samambaia, 314, Goiânia, GO, 74001-970, Brazil.
Ricardo MenegattiFaculty of Pharmacy, Laboratory of Medicinal Pharmaceutical Chemistry, Federal University of Goiás, Goiânia, GO, Brazil. rm_rj@yahoo.com.
Universidade Federal de Goiás · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThis study investigates the anti-nociceptive and anti-inflammatory effects of new piperazine compound (LQFM182) as well as the toxicity acute in vitro. MAIN

methodsTo evaluate the anti-nociceptive activity, the acetic acid-induced abdominal writhing test, tail flick test and formalin-induced pain test were used. The anti-inflammatory activity was evaluated using the models of paw oedema and pleurisy induced by carrageenan and some inflammatory parameters were evaluated, including cell migration, myeloperoxidase enzyme activity and the levels of TNF-α and IL-1β cytokines in pleural exudate. The acute oral systemic toxicity of LQFM182 in mice was evaluated through the neutral red uptake (nru) assay. KEY

findingsLQFM182 (50, 100 or 200 mg/kg, p.o.) decreased the number of writhings induced by acetic acid in a dose-dependent manner, and an intermediate dose (100 mg/kg, p.o.) reduced the paw licking time of animals in the second phase of the formalin test. Furthermore, LQFM182 (100 mg/kg, p.o.) reduced oedema formation at all hours of the paw oedema induced by carrageenan test and in pleurisy test reduced cell migration from the reduction of polymorphonuclear cells, myeloperoxidase enzyme activity and the levels of pro-inflammatory cytokines IL-1β and TNF-α. Therefore, it was classified in GHS category 300 < LD SIGNIFICANCE: Reduction of the TNF-α and IL-1β levels.

Indexed as

AnalgesicsAnimalsAnti-Inflammatory AgentsBALB 3T3 CellsCarrageenanCell LineCell MovementEdemaFemaleInterleukin-1betaMicePainPain MeasurementPiperazinePiperazinesPleurisyAnalgesicsAnti-Inflammatory AgentsCarrageenanInterleukin-1betaPiperazinePiperazinespyrazolePyrazolesTumor Necrosis Factor-alphaAnti-inflammatoryIL-1βN-arylheterocyclesTNF-α

Identifiers

PMID28825161
OpenAlexW2748221130

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.