Evidence map›Paper›PMID 35257283›Full record

ArticleInflammopharmacology2022

Oral administration of essential oil from Psidium glaziovianum Kiaersk leaves alleviates pain and inflammation in mice.

Wêndeo Kennedy Costa, Matheus Ferreira do Nascimento, Cícero Ramon Bezerra Dos Santos, Júlio César Ribeiro Dede Oliveira FariasAguiar, Daniela Maria do Amaral Ferraz Navarro, Thiago Henrique Napoleão, Maria Tereza Dos Santos Correia, Fábio André Brayner, Alisson Macário de Oliveira, Márcia Vanusa da Silva

Abstract read
PubMed Publisher
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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

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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.

Wêndeo Kennedy CostaDepartamento de Bioquímica, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil. wendeocosta@gmail.com.ORCID http://orcid.org/0000-0001-7925-6794
Matheus Ferreira do NascimentoDepartamento de Bioquímica, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Cícero Ramon Bezerra Dos SantosDepartamento de Bioquímica, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Júlio César Ribeiro Dede Oliveira FariasAguiarDepartamento de Química Fundamental, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Daniela Maria do Amaral Ferraz NavarroDepartamento de Química Fundamental, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Thiago Henrique NapoleãoDepartamento de Bioquímica, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Maria Tereza Dos Santos CorreiaDepartamento de Química Fundamental, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Fábio André BraynerInstituto Aggeu Magalhães, Fundação Oswaldo Cruz, Recife, PE, 50670-420, Brazil.
Alisson Macário de OliveiraDepartamento de Bioquímica, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Márcia Vanusa da SilvaDepartamento de Bioquímica, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Universidade Federal de Pernambuco · BR

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 01Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco BFP-0122-4.03/19
6 · The paper itself

Abstract

Plants of the genus Psidium have been employed in "in natura" consumption and agroindustry, and owing to the diversity of phytochemicals, the development of new pharmaceutical forms has received remarkable research interest. In this study, the essential oil obtained from Psidium glaziovianum (PgEO) leaves were evaluated antinociceptive and anti-inflammatory activities were evaluated in mouse models. Initially, PgEO was characterized by gas chromatography-mass spectrometry and gas chromatography with flame ionization detection, and the profile was dominated by sesquiterpene compounds. In the evaluation of acute antinociceptive activity (abdominal contortions induced by acetic acid, formalin, tail immersion, and hot plate tests), PgEO promoted a reduction in nociception in the chemical and thermal models. Additionally, the potential underlying mechanism was investigated using pain pathway blockers, and the results revealed a combined action of opioidergic and muscarinic pathways. The anti-inflammatory potential was confirmed by anti-edematogenic action, reduced cell migration, pro-inflammatory cytokine production, and granuloma formation in chronic processes. This study provides evidence that PgEO can be effective for the treatment of pain and acute and chronic inflammation.

Indexed as

Oils, VolatilePsidiumAdministration, OralAnalgesicsAnimalsEdemaInflammationMicePainPlant ExtractsPlant LeavesAnalgesicsOils, VolatilePlant ExtractsAnti-inflammatory activityAntinociceptive activityAraçá-doceEssential oilMyrtaceae

Identifiers

PMID35257283
OpenAlexW4220726256

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.