Evidence map›Paper›PMID 36094726›Full record

ArticleInflammopharmacology2022

Essential oil from the leaves of Eugenia pohliana DC. (Myrtaceae) alleviate nociception and acute inflammation in mice.

Andreza Larissa do Nascimento, Joyce Bezerra Guedes, Wêndeo Kennedy Costa, Bruno Oliveira de Veras, Júlio César Ribeiro de Oliveira Farias de Aguiar, Daniela Maria do Amaral Ferraz Navarro, Maria Tereza Dos Santos Correia, Thiago Henrique Napoleão, Alisson Macário de Oliveira, Márcia Vanusa da Silva

Abstract read
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In one paragraph

Article in Inflammopharmacology, 2022. 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
1.0field-weighted citation impact, top 23% 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, 7 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 1 institution in 1 country.

Andreza Larissa do NascimentoDepartment of Biochemistry, Federal University of Pernambuco, Recife, Pernambuco, 50670-420, Brazil. andrezanascimento46@gmail.com.ORCID http://orcid.org/0000-0002-3567-1336
Joyce Bezerra GuedesDepartment of Biochemistry, Federal University of Pernambuco, Recife, Pernambuco, 50670-420, Brazil.
Wêndeo Kennedy CostaDepartment of Biochemistry, Federal University of Pernambuco, Recife, Pernambuco, 50670-420, Brazil.
Bruno Oliveira de VerasDepartment of Tropical Medicine, Laboratory of Microbiology, Federal University of Pernambuco, Recife, Pernambuco, 50670-420, Brazil.
Júlio César Ribeiro de Oliveira Farias de AguiarFundamental Chemistry Department, Federal University of Pernambuco, Recife, Pernambuco, 50740-540, Brazil.
Daniela Maria do Amaral Ferraz NavarroFundamental Chemistry Department, Federal University of Pernambuco, Recife, Pernambuco, 50740-540, Brazil.
Maria Tereza Dos Santos CorreiaDepartment of Biochemistry, Federal University of Pernambuco, Recife, Pernambuco, 50670-420, Brazil.
Thiago Henrique NapoleãoDepartment of Biochemistry, Federal University of Pernambuco, Recife, Pernambuco, 50670-420, Brazil.
Alisson Macário de OliveiraDepartment of Biochemistry, Federal University of Pernambuco, Recife, Pernambuco, 50670-420, Brazil.
Márcia Vanusa da SilvaDepartment of Biochemistry, Federal University of Pernambuco, Recife, Pernambuco, 50670-420, Brazil.
Universidade Federal de Pernambuco · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eugenia pohliana DC.(Myrtaceae) is used in folk medicine by communities in Brazil. However, there are no reports on its biological activity. This is the first study to identify the components of E. pohliana essential oil (EpEO) and evaluate their antinociceptive and anti-inflammatory activities in an in vivo model at doses of 25, 50, and 100 mg/kg. The essential oil (EO) was obtained by hydrodistillation, and the analysis was performed by gas chromatography coupled with mass spectrometry. Antinociceptive activity was evaluated by writhing tests, tail movement, and formalin (neurogenic and inflammatory pain); naloxone was used to determine the nociception mechanism. Anti-inflammatory activity was assessed by oedema and peritonitis tests. We found that (E)-β-caryophyllene (BCP) (15.56%), δ-cadinene (11.24%) and α-cadinol (10.89%) were the major components. In the writhing test, there was a decrease in writing by 42.95-70.70%, in the tail movement, an increase in latency time by 69.12-86.63%, and in the formalin test, there was a reduction in pain neurogenic by 29.54-61.74%, and inflammatory pain by 37.42-64.87%. The antinociceptive effect of EpEO occurs through the activation of opioid receptors. In addition, a reduction in inflammation by 74.93‒81.41% was observed in the paw edema test and inhibition of the influx of leukocytes by 51.86‒70.38% and neutrophils by 37.74‒54.72% in the peritonitis test. It was concluded that EpEO has antinociceptive effect by the opioid pathway, as shown by the inhibitory effect of naloxone, and anti-inflammatory actions, and that its use does not cause hemolytic damage or behavioral change.

Indexed as

EugeniaMyrtaceaeOils, VolatilePeritonitisAnalgesicsAnimalsAnti-Inflammatory AgentsEdemaInflammationMiceNaloxoneNociceptionPainPlant ExtractsAnalgesicsAnti-Inflammatory AgentsNaloxoneOils, VolatilePlant ExtractsAnalgesicAnti-inflammatoryCaatingaβ (E)-caryophyllene

Identifiers

PMID36094726
OpenAlexW4296554571

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.