Evidence map›Paper›PMID 36357780›Full record

ArticleScientific reports2022

β-caryophyllene and docosahexaenoic acid, isolated or associated, have potential antinociceptive and anti-inflammatory effects in vitro and in vivo.

Laís Ferraz Brito Sousa, Hellen Braga Martins Oliveira, Nathan das Neves Selis, Lorena Lobo Brito Morbeck, Talita Costa Santos, Lucas Santana Coelho da Silva, Jully Chayra Santos Viana, Mariane Mares Reis, Beatriz Almeida Sampaio, Guilherme Barreto Campos and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 16 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

13 authors at 3 institutions in 1 country.

Laís Ferraz Brito SousaMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil.
Hellen Braga Martins OliveiraUniversity of Santa Cruz (UESC), Campus Soane Nazaré de Andrade, Ilhéus, Brazil.
Nathan das Neves SelisUniversity of Santa Cruz (UESC), Campus Soane Nazaré de Andrade, Ilhéus, Brazil.
Lorena Lobo Brito MorbeckMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil.
Talita Costa SantosMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil.
Lucas Santana Coelho da SilvaUniversity of Santa Cruz (UESC), Campus Soane Nazaré de Andrade, Ilhéus, Brazil.
Jully Chayra Santos VianaMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil.
Mariane Mares ReisMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil.
Beatriz Almeida SampaioMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil.
Guilherme Barreto CamposMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil.
Jorge TimenetskyDepartment of Microbiology, Institute of Biomedical Science, University of São Paulo, São Paulo, Brazil.
Regiane YatsudaMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil.
Lucas Miranda MarquesMultidisciplinary Institute of Health, Federal University of Bahia (UFBA), Rua Rio de Contas, 58 - Quadra 17 - Lote 58, Bairro Candeias, CEP: 45.029-094, Vitória da Conquista, BA, Brazil. lucasm@ufba.br.
Universidade Federal da Bahia · BRUniversidade Estadual de Santa Cruz · BRUniversidade de São Paulo · BR

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Code 001Fundação de Amparo à Pesquisa do Estado da Bahia JCB0035/2016
6 · The paper itself

Abstract

Inflammation is a complex biological response involving the immune, autonomic, vascular, and somatosensory systems that occurs through the synthesis of inflammatory mediators and pain induction by the activation of nociceptors. Staphylococcus aureus, the main cause of bacteremia, is one of the most common and potent causes of inflammation in public health, with worse clinical outcomes in hospitals. Antioxidant substances have been evaluated as alternative therapeutic analgesics, antioxidants, anti-inflammatory agents, antitumor agents, and bactericides. Among these, we highlight the essential oils of aromatic plants, such as β-caryophyllene (BCP), and polyunsaturated fatty acids, such as docosahexaenoic acid (DHA). The objective of this study was to evaluate the biological activities of BCP-DHA association in in vitro and in vivo experimental models of antinociception and inflammation. To determine the anti-inflammatory effects, monocytes isolated from the peripheral blood of adult male volunteers were infected with methicillin-resistant S. aureus and incubated with treatment for cytokine dosage and gene expression analysis. Antinociceptive effects were observed in the three models when comparing the control (saline) and the BCP-DHA treatment groups. For this purpose, the antinociceptive effects were evaluated in animal models using the following tests: acetic acid-induced abdominal writhing, paw edema induced by formalin intraplantar injection, and von Frey hypernociception. There was a significant reduction in the GM-CSF, TNFα, IL-1, IL-6, and IL-12 levels and an increase in IL-10 levels in the BCP-DHA treatment groups, in addition to negative regulation of the expression of the genes involved in the intracellular inflammatory signaling cascade (IL-2, IL-6, IRF7, NLRP3, and TYK2) in all groups receiving treatment, regardless of the presence of infection. Statistically significant results (p < 0.05) were obtained in the acetic acid-induced abdominal writhing test, evaluation of paw edema, evaluation of paw flinching and licking in the formalin intraplantar injection model, and the von Frey hypernociception test. Therefore, BCP and DHA, either administered individually or combined, demonstrate potent anti-inflammatory and antinociceptive effects.

Indexed as

Docosahexaenoic AcidsMethicillin-Resistant Staphylococcus aureusAnalgesicsAnimalsAnti-Inflammatory AgentsAntioxidantsEdemaFormaldehydeInflammationInterleukin-6Plant ExtractsPolycyclic SesquiterpenesAnalgesicsAnti-Inflammatory AgentsAntioxidantscaryophylleneDocosahexaenoic AcidsFormaldehydeInterleukin-6Plant ExtractsPolycyclic Sesquiterpenes

Identifiers

PMID36357780
PMCPMC9649594
OpenAlexW4309243354

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.