Evidence map›Paper›PMID 35347522›Full record

ArticleInflammopharmacology2022

Scyphocephalione A isolated from the stem bark of Scyphocephalium ochocoa (Myristicaceae) attenuate acute and chronic pain through the antiinflammatory activity.

Marius Mbiantcha, Raymond Guy Feuya Tchouya, William Nana Yousseu, Donatien Albert Atsamo, Hibrahim Foundikou, Jacques Lebibi, Franklin Gamo Zemo

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. International journal of inflammation · 2023
    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

7 authors at 3 institutions in 2 countries.

Marius MbiantchaLaboratory of Animal Physiology and Phytopharmacology, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon. mbiantchamarius@yahoo.fr.ORCID http://orcid.org/0000-0001-8586-6150
Raymond Guy Feuya TchouyaFaculty of Science, Department of Chemistry, Universite Des Sciences Et Techniques de Masuku, Franceville, Gabon.
William Nana YousseuLaboratory of Animal Physiology and Phytopharmacology, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
Donatien Albert AtsamoDepartment of Animal Biology and Physiology, Faculty of Science, University of Yaounde I, PO Box 812, Yaoundé, Cameroon.
Hibrahim FoundikouFaculty of Science, Department of Chemistry, Universite Des Sciences Et Techniques de Masuku, Franceville, Gabon.
Jacques LebibiFaculty of Science, Department of Chemistry, Universite Des Sciences Et Techniques de Masuku, Franceville, Gabon.
Franklin Gamo ZemoDepartment of Psychology, Faculty of Arts, Letters and Social Sciences, University of Yaoundé I, P.O. Box 7011, Yaoundé, Cameroon.
Université des Sciences et Techniques de Masuku · GAUniversité de Dschang · CMUniversité de Yaoundé I · CM

Funding

TWAS-ICCBS RF N°: 3240280477
6 · The paper itself

Abstract

In the treatment of cancer, patients that receive anti-cancer drugs such as Vincristine develop peripheral neuropathic pain. Scyphocephalione A is a new bioactive compound isolated from Scyphocephalium ochocoa (Myristicaceae), a medicinal plant traditionally used in African countries. Recently, an in vitro study has shown its anti-inflammatory and cytotoxic activities on MCF-7 cell line of mammary carcinoma. The purpose of the present study was to assess the in vitro anti-inflammatory and in vivo anti-nociceptive activities of Scyphocephalione A. In vitro tests were carried out on cyclooxygenase and 5-lipoxygenase activities, and on protein denaturation; while in vivo tests were performed on acute and chronic pain models. It was noticed that Scyphocephalione A (1000 µg/ml), inhibits proteins denaturation, cyclooxygenase and 5-lipoxygenase activities respectively by 74.21%, 75.80% and 64.43%. The dose 50 mg/kg of Scyphocephalione A, inhibits acetic acid (63.43%, p < 0.001) and formalin (42.12%, p < 0.001) within first phase and 67.53% (p < 0.001) within second phase)-induced pains. At the same dose, Scyphocephalione A significantly inhibited mechanical and heat hyperalgesia, as well as cold allodynia induced by vincristine. In addition, the compound restored haematological, biochemical and oxidative stress parameters which were altered following Vincristine administration. These results suggest that Scyphocephalione A is endowed with anti-inflammatory potential and antinociceptive properties. Therefore, Scyphocephalione A can be classified as a promising molecule for the management of peripheral neuropathic pain triggered by anti-cancer drug.

Indexed as

Antineoplastic AgentsChronic PainMyristicaceaeNeuralgiaAnalgesicsAnimalsAnti-Inflammatory AgentsArachidonate 5-LipoxygenaseCyclooxygenase 2Disease Models, AnimalHumansHyperalgesiaPlant BarkVincristineAnalgesicsAnti-Inflammatory AgentsAntineoplastic AgentsArachidonate 5-LipoxygenaseCyclooxygenase 2VincristineAcute painNeuropathic painScyphocephalione AScyphocephalium ochocoa

Identifiers

PMID35347522
OpenAlexW4221098905

What OpenQuestion holds

Textmetadata
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Registered trials

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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.