Evidence map›Paper›PMID 33287119›Full record

ArticleInternational journal of molecular sciences2020

Carvone Enantiomers Differentially Modulate IgE-Mediated Airway Inflammation in Mice.

Jaime Ribeiro-Filho, Juliana da Silva Brandi, Hermann Ferreira Costa, Karina Carla de Paula Medeiros, Jacqueline Alves Leite, Damião Pergentino de Sousa, Márcia Regina Piuvezam

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
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  4. An Effective and Promising Strategy for Plant Protection: Synthesis ofInternational journal of molecular sciences · 2024
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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

7 authors at 3 institutions in 1 country.

Jaime Ribeiro-FilhoLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ, Salvador 40296-710, Brazil.ORCID 0000-0003-3126-6509
Juliana da Silva BrandiDepartamento de Farmácia, Centro de Ciências da Saúde, Unifaminas Centro Universitário, Muriaé 36880-000, Brazil.
Hermann Ferreira CostaFaculdade de Medicina Nova Esperança, João Pessoa 58067-695, Brazil.
Karina Carla de Paula MedeirosDepartamento de Morfologia, Centro de Biociências, UFRN, Natal 59072-970, Brazil.
Jacqueline Alves LeiteDepartamento de Farmacologia, Instituto de Ciências Biológicas, UFG, Goiânia 74690-900, Brazil.
Damião Pergentino de SousaDepartamento de Ciências Farmacêuticas, Centro de Ciências da Saúde, UFPB, João Pessoa 58051-900, Brazil.ORCID 0000-0002-7180-4896
Márcia Regina PiuvezamLaboratório de Imunofarmacologia, Departamento de Fisiologia e Patologia, UFPB, João Pessoa 58051-900, Brazil.
Universidade Federal da Paraíba · BRFundação Oswaldo Cruz · BRUniversidade Federal do Rio Grande do Norte · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carvone is a monoterpene found in nature in the form of enantiomers (S- and R-). While previous research has demonstrated the anti-inflammatory and anti-allergic effects of carvone, the influence of carvone enantiomeric composition on its anti-allergic activity remains to be investigated. This study aimed to evaluate the anti-allergic activity of carvone enantiomers in a murine model of airway allergic inflammation induced by sensitization and challenge with ovalbumin (OVA). The oral treatment with R-carvone or S-carvone 1 h before each challenge inhibited the number of leukocytes and eosinophils in the bronchoalveolar lavage (BAL). R-carvone inhibited leukocyte infiltration and mucus production in the lung, which was correlated with decreased production of OVA-specific IgE in the serum and increased concentrations of IL-10 in the BAL. On the other hand, the administration of S-carvone had little inhibitory effect on inflammatory infiltration and mucus production in the lung, which might be associated with increased production of IFN-γ in the BAL. When administered 1 h before each sensitization, both enantiomers inhibited eosinophil recruitment to the BAL but failed in decreasing the titers of IgE in the serum of allergic mice. Our data indicate that carvone enantiomers differentially modulated IgE-mediated airway inflammation in mice. In conclusion, unlike S-carvone, R-carvone has the potential to be used in anti-allergic drug development.

Indexed as

AnimalsAnti-Inflammatory AgentsChemotaxisCyclohexane MonoterpenesCytokinesDisease Models, AnimalEosinophilsImmunoglobulin EImmunomodulationInflammationLungMiceRespiratory Tract DiseasesSeverity of Illness IndexAnti-Inflammatory AgentscarvoneCyclohexane MonoterpenesCytokinesImmunoglobulin Eairway inflammationanti-allergiccarvoneenantiomerseosinophilsterpenes

Identifiers

PMID33287119
PMCPMC7731315
OpenAlexW3110270946

What OpenQuestion holds

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LicenceCC BY
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.