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In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde

BACKGROUND: Perillaldehyde and cinnamaldehyde are natural substances found in plants that are used as flavoring ingredients. Due to the α,β-unsaturated aldehydes in their structures, these compounds are expected to be DNA reactive. Indeed, several reports have indicated that perillaldehyde and cinna...

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Autores principales: Honma, Masamitsu, Yamada, Masami, Yasui, Manabu, Horibata, Katsuyoshi, Sugiyama, Kei-ichi, Masumura, Kenichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284016/
https://www.ncbi.nlm.nih.gov/pubmed/34271990
http://dx.doi.org/10.1186/s41021-021-00204-3
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author Honma, Masamitsu
Yamada, Masami
Yasui, Manabu
Horibata, Katsuyoshi
Sugiyama, Kei-ichi
Masumura, Kenichi
author_facet Honma, Masamitsu
Yamada, Masami
Yasui, Manabu
Horibata, Katsuyoshi
Sugiyama, Kei-ichi
Masumura, Kenichi
author_sort Honma, Masamitsu
collection PubMed
description BACKGROUND: Perillaldehyde and cinnamaldehyde are natural substances found in plants that are used as flavoring ingredients. Due to the α,β-unsaturated aldehydes in their structures, these compounds are expected to be DNA reactive. Indeed, several reports have indicated that perillaldehyde and cinnamaldehyde show positive in in vitro and in vivo genotoxicity tests. However, their genotoxic potentials are currently disputed. To clarify the mutagenicity of perillaldehyde and cinnamaldehyde, we conducted in silico quantitative structure–activity relationship (QSAR) analysis, in vitro Ames tests, and in vivo transgenic rodent gene mutation (TGR) assays. RESULTS: In Ames tests, perillaldehyde was negative and cinnamaldehyde was positive; these respective results were supported by QSAR analysis. In TGR assays, we treated Muta™ Mice with perillaldehyde and gpt-delta mice with cinnamaldehyde up to the maximum tested doses (1000 mg/kg/day). There was no increase in gene mutations in the liver, glandular stomach, or small intestine following all treatments except the positive control (N-ethyl-N-nitrosourea at 100 mg/kg/day). CONCLUSIONS: These data clearly show no evidence of in vivo mutagenic potentials of perillaldehyde and cinnamaldehyde (administered up to 1000 mg/kg/day) in mice; however, cinnamaldehyde is mutagenic in vitro.
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spelling pubmed-82840162021-07-19 In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde Honma, Masamitsu Yamada, Masami Yasui, Manabu Horibata, Katsuyoshi Sugiyama, Kei-ichi Masumura, Kenichi Genes Environ Research BACKGROUND: Perillaldehyde and cinnamaldehyde are natural substances found in plants that are used as flavoring ingredients. Due to the α,β-unsaturated aldehydes in their structures, these compounds are expected to be DNA reactive. Indeed, several reports have indicated that perillaldehyde and cinnamaldehyde show positive in in vitro and in vivo genotoxicity tests. However, their genotoxic potentials are currently disputed. To clarify the mutagenicity of perillaldehyde and cinnamaldehyde, we conducted in silico quantitative structure–activity relationship (QSAR) analysis, in vitro Ames tests, and in vivo transgenic rodent gene mutation (TGR) assays. RESULTS: In Ames tests, perillaldehyde was negative and cinnamaldehyde was positive; these respective results were supported by QSAR analysis. In TGR assays, we treated Muta™ Mice with perillaldehyde and gpt-delta mice with cinnamaldehyde up to the maximum tested doses (1000 mg/kg/day). There was no increase in gene mutations in the liver, glandular stomach, or small intestine following all treatments except the positive control (N-ethyl-N-nitrosourea at 100 mg/kg/day). CONCLUSIONS: These data clearly show no evidence of in vivo mutagenic potentials of perillaldehyde and cinnamaldehyde (administered up to 1000 mg/kg/day) in mice; however, cinnamaldehyde is mutagenic in vitro. BioMed Central 2021-07-16 /pmc/articles/PMC8284016/ /pubmed/34271990 http://dx.doi.org/10.1186/s41021-021-00204-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Honma, Masamitsu
Yamada, Masami
Yasui, Manabu
Horibata, Katsuyoshi
Sugiyama, Kei-ichi
Masumura, Kenichi
In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde
title In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde
title_full In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde
title_fullStr In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde
title_full_unstemmed In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde
title_short In vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde
title_sort in vivo and in vitro mutagenicity of perillaldehyde and cinnamaldehyde
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284016/
https://www.ncbi.nlm.nih.gov/pubmed/34271990
http://dx.doi.org/10.1186/s41021-021-00204-3
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