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Investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems

Several antioxidant food additives are added to oils, soups, sauces, chewing gum, potato chips, and so on. One of them is octyl gallate. The purpose of this study was to evaluate the potential genotoxicity of octyl gallate in human lymphocytes, using in vitro chromosomal abnormalities (CA), sister c...

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Autores principales: Avuloglu Yilmaz, Ece, Yuzbasioglu, Deniz, Unal, Fatma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281373/
https://www.ncbi.nlm.nih.gov/pubmed/36882025
http://dx.doi.org/10.1093/mutage/gead005
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author Avuloglu Yilmaz, Ece
Yuzbasioglu, Deniz
Unal, Fatma
author_facet Avuloglu Yilmaz, Ece
Yuzbasioglu, Deniz
Unal, Fatma
author_sort Avuloglu Yilmaz, Ece
collection PubMed
description Several antioxidant food additives are added to oils, soups, sauces, chewing gum, potato chips, and so on. One of them is octyl gallate. The purpose of this study was to evaluate the potential genotoxicity of octyl gallate in human lymphocytes, using in vitro chromosomal abnormalities (CA), sister chromatid exchange (SCE), cytokinesis block micronucleus cytome (CBMN-Cyt), micronucleus-FISH (MN-FISH), and comet tests. Different concentrations (0.031, 0.063, 0.125, 0.25, and 0.50 μg/ml) of octyl gallate were used. A negative (distilled water), a positive (0.20 μg/ml Mitomycin-C), and a solvent control (8.77 μl/ml ethanol) were also applied for each treatment. Octyl gallate did not cause changes in chromosomal abnormalities, micronucleus, nuclear bud (NBUD), and nucleoplasmic bridge (NPB) frequency. Similarly, there was no significant difference in DNA damage (comet assay), percentage of centromere positive and negative cells (MN-FISH test) compared to the solvent control. Moreover, octyl gallate did not affect replication and nuclear division index. On the other hand, it significantly increased the SCE/cell ratio in three highest concentrations compared to solvent control at 24 h treatment. Similarly, at 48 h treatment, the frequency of SCE raised significantly compared to solvent controls at all the concentrations (except 0.031 μg/ml). An important reduction was detected in mitotic index values in the highest concentration at 24 h treatment and almost all concentrations (except 0.031 and 0.063 µg/ml) at 48 h treatment. The results obtained suggest that octyl gallate has no important genotoxicological action on human peripheral lymphocytes at the concentrations applied in this study.
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spelling pubmed-102813732023-06-21 Investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems Avuloglu Yilmaz, Ece Yuzbasioglu, Deniz Unal, Fatma Mutagenesis Original Manuscripts Several antioxidant food additives are added to oils, soups, sauces, chewing gum, potato chips, and so on. One of them is octyl gallate. The purpose of this study was to evaluate the potential genotoxicity of octyl gallate in human lymphocytes, using in vitro chromosomal abnormalities (CA), sister chromatid exchange (SCE), cytokinesis block micronucleus cytome (CBMN-Cyt), micronucleus-FISH (MN-FISH), and comet tests. Different concentrations (0.031, 0.063, 0.125, 0.25, and 0.50 μg/ml) of octyl gallate were used. A negative (distilled water), a positive (0.20 μg/ml Mitomycin-C), and a solvent control (8.77 μl/ml ethanol) were also applied for each treatment. Octyl gallate did not cause changes in chromosomal abnormalities, micronucleus, nuclear bud (NBUD), and nucleoplasmic bridge (NPB) frequency. Similarly, there was no significant difference in DNA damage (comet assay), percentage of centromere positive and negative cells (MN-FISH test) compared to the solvent control. Moreover, octyl gallate did not affect replication and nuclear division index. On the other hand, it significantly increased the SCE/cell ratio in three highest concentrations compared to solvent control at 24 h treatment. Similarly, at 48 h treatment, the frequency of SCE raised significantly compared to solvent controls at all the concentrations (except 0.031 μg/ml). An important reduction was detected in mitotic index values in the highest concentration at 24 h treatment and almost all concentrations (except 0.031 and 0.063 µg/ml) at 48 h treatment. The results obtained suggest that octyl gallate has no important genotoxicological action on human peripheral lymphocytes at the concentrations applied in this study. Oxford University Press 2023-03-07 /pmc/articles/PMC10281373/ /pubmed/36882025 http://dx.doi.org/10.1093/mutage/gead005 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Manuscripts
Avuloglu Yilmaz, Ece
Yuzbasioglu, Deniz
Unal, Fatma
Investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems
title Investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems
title_full Investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems
title_fullStr Investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems
title_full_unstemmed Investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems
title_short Investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems
title_sort investigation of genotoxic effect of octyl gallate used as an antioxidant food additive in in vitro test systems
topic Original Manuscripts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281373/
https://www.ncbi.nlm.nih.gov/pubmed/36882025
http://dx.doi.org/10.1093/mutage/gead005
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