Evidence map›Paper›PMID 39635437›Full record

ArticleFrontiers in pharmacology2024

Chemical characterization, assessment of acute oral toxicity, and antinociceptive potential of the methanolic extract of

Wellington Junior Taisho Nagahama Costa, Leticia Prazeres de Farias Coelho, Alan Luz Tembra, Rayan Fidel Martins Monteiro, Jose Ramon Gama Almeida, Klinsmann Thiago Lima, Anderson de Santana Botelho, Raimundo Junior da Rocha Batista, Jofre Jacob da Silva Freitas, Wandson Braamcamp de Souza Pinheiro and 5 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Wellington Junior Taisho Nagahama CostaLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Leticia Prazeres de Farias CoelhoLaboratory of Morphophysiology Applied to Health, Department of Morphology and Physiological Sciences, State University of Pará, Belém, Brazil.
Alan Luz TembraLaboratory of Morphophysiology Applied to Health, Department of Morphology and Physiological Sciences, State University of Pará, Belém, Brazil.
Rayan Fidel Martins MonteiroLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Jose Ramon Gama AlmeidaLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Klinsmann Thiago LimaLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Anderson de Santana BotelhoLaboratory of Chemical Analysis, Coordination of Earth Sciences and Ecology, Emílio Goeldi Museum, Belém, Brazil.
Raimundo Junior da Rocha BatistaLaboratory of Chemical Analysis, Coordination of Earth Sciences and Ecology, Emílio Goeldi Museum, Belém, Brazil.
Jofre Jacob da Silva FreitasLaboratory of Morphophysiology Applied to Health, Department of Morphology and Physiological Sciences, State University of Pará, Belém, Brazil.
Wandson Braamcamp de Souza PinheiroLaboratory of Central Extraction, Institute of Exact and Natural Sciences, Federal University of Pará, Belém, Brazil.
Fabiola Raquel Tenorio OliveiraLaboratory of Morphophysiology Applied to Health, Department of Morphology and Physiological Sciences, State University of Pará, Belém, Brazil.
Karen Renata Herculano Matos OliveiraLaboratory of Experimental Neuropharmacology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Anderson Bentes de LimaLaboratory of Morphophysiology Applied to Health, Department of Morphology and Physiological Sciences, State University of Pará, Belém, Brazil.
Cristine Bastos do AmaranteLaboratory of Chemical Analysis, Coordination of Earth Sciences and Ecology, Emílio Goeldi Museum, Belém, Brazil.
Gilmara de Nazareth Tavares BastosLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Aim of the study: This study aimed to chemically characterize the methanolic extract of Materials and methods: The leaves were collected during the rainy season, and the methanolic extract was obtained after gradient extraction using different solvents. MEMLL was analyzed using high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR). Acute oral toxicity testing followed the Organization for Economic Co-operation and Development (OECD) guideline 423. Subsequently, acetic acid, hot plate, and formalin tests were used to evaluate the analgesic effects. Results: In the chemical characterization of MEMLL by HPLC, three flavonoids were identified: rutin, quercetin, and epicatechin. In addition, when NMR spectroscopy was performed, rutin and quercetin were again identified, as well as the chemical compounds luteolin and chrysoeriol. In the acute oral toxicity test, MEMLL showed no physiological or behavioral changes. In the nociceptive study, MEMLL showed an effect at doses of 50 and 100 mg/kg in the 0.6% acetic acid test, i.e., 51.46% and 75.08%, respectively. In the hot plate test, the MEMLL group at a dose of 50 mg/kg was effective at times of 30 and 60 min, i.e., 164.43% and 122.95%, respectively. Similarly, the MEMLL group at a dose of 100 mg/kg was also effective in increasing latency at times of 30 and 60 min, i.e., 162.62% and 136.68%, respectively. In the formalin test, MEMLL showed an antinociceptive effect on neurogenic pain at doses of 50 and 100 mg/kg when compared to the control group, 35.25% and 52.30%, respectively. In the inflammatory phase, inhibition was observed in the MEMLL at doses of 50 and 100 mg/kg, i.e., 66.39% and 72.15%, respectively. Conclusion: MEMLL has analgesic properties and is non-toxic, validating the Brazilian ethnopharmacological use of this plant for pain treatment. The leaves of the species

Indexed as

acute oral toxicityantinociceptiveflavonoidmedicinal plantMontrichardia linifera

Identifiers

PMID39635437
PMCPMC11615642

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