Evidence map›Paper›PMID 31852517›Full record

ArticleBMC pharmacology & toxicology2019

Gamma-hexalactone flavoring causes DNA lesion and modulates cytokines secretion at non-cytotoxic concentrations.

Luísa Zuravski, Taiane A Escobar, Elizandra G Schmitt, Queila D F Amaral, Fávero R Paula, Thiago Duarte, Marta M M F Duarte, Michel M Machado, Luís F S Oliveira, Vanusa Manfredini

Open access · goldAbstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 81% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

10 authors at 3 institutions in 1 country.

Luísa ZuravskiPrograma de Pós-Graduação em Bioquímica, Universidade Federal do Pampa, Uruguaiana, Brazil. luisazuravski@unipampa.edu.br.
Taiane A EscobarPrograma de Pós-Graduação em Bioquímica, Universidade Federal do Pampa, Uruguaiana, Brazil.
Elizandra G SchmittCurso de Farmácia, Universidade Federal do Pampa, Uruguaiana, Brazil.
Queila D F AmaralPrograma de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Pampa, Uruguaiana, Brazil.
Fávero R PaulaCurso de Farmácia, Universidade Federal do Pampa, Uruguaiana, Brazil.
Thiago DuartePrograma de Pós-Graduação em Farmacologia, Centro de Ciências da Saúde, Universidade Federal de Santa Maria, Santa Maria, Brazil.
Marta M M F DuarteUniversidade Luterana do Brasil, Santa Maria, Brazil.
Michel M MachadoCurso de Farmácia, Universidade Federal do Pampa, Uruguaiana, Brazil.
Luís F S OliveiraCurso de Farmácia, Universidade Federal do Pampa, Uruguaiana, Brazil.
Vanusa ManfrediniPrograma de Pós-Graduação em Bioquímica, Universidade Federal do Pampa, Uruguaiana, Brazil.
Universidade Federal do Pampa · BRUniversidade Federal de Santa Maria · BRUniversidade Luterana do Brasil · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe γ-hexalactone is a flavoring agent for alcoholic beverages, teas, breads, dairy products, coffees, buttery products among others. It presents low molecular weight and exhibits sweet fruity aroma with nuances of nuts. As far as we know, both literature and government regulations have gaps regarding the safe use of the γ-hexalactone. In this context, the main objective of this work was to evaluate the effects of γ-hexalactone through in silico and in vitro approaches.

methodsThe in silico analysis was performed through four free online platforms (admetSAR, Osiris Property Explorer

resultsThe platform PreADMET pointed out that γ-hexalactone is potentially mutagenic and carcinogenic. The comet assay data corroborate with these results demonstrating that γ-hexalactone at 5.15 μM caused lymphocytes DNA damage. In relation to cytokine secretion, the results indicate that lymphocytes were activated by γ-hexalactone at non-cytotoxic concentrations, involving an increase in the IL-1 levels in all tested concentrations, ranging from approximately 56 to 93%. The γ-hexalactone only at 5.15 μM induced increase in the levels of IL-6 (~ 60%), TNF-α (~ 68%) and IFN-γ (~ 29%), but decreased IL-10 (~ 46%) in comparison with the negative control (p < 0.05). No change was observed in total lymphocytes or in cell viability at the concentrations tested.

conclusionsIn summary, the γ-hexalactone demonstrated immunomodulatory and genotoxic effects at non-cytotoxic concentrations in healthy lymphocytes.

Indexed as

DNA DamageAdultCell ProliferationCells, CulturedCell SurvivalComet AssayComputer SimulationCytokinesDose-Response Relationship, DrugFlavoring AgentsHumansInhibitory Concentration 50LactonesLeukocytes, MononuclearMicronuclei, Chromosome-DefectiveMutagens4-hexanolideCytokinesFlavoring AgentsLactonesMutagensFlavoringIn silicoIn vitroLymphocytesγ-Hexalactone

Identifiers

PMID31852517
PMCPMC6921379
OpenAlexW2995651476

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LicenceCC BY
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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.