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In Vitro Genotoxicity Assessment of a Novel Resveratrol Analogue, HS-1793
Resveratrol has received considerable attention as a polyphenol with various biological effects such as anti-inflammatory, anti-oxidant, anti-mutagenic, anti-carcinogenic, and cardioprotective properties. As part of the overall safety assessment of HS-1793, a novel resveratrol analogue free from the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society Of Toxicology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206749/ https://www.ncbi.nlm.nih.gov/pubmed/25343016 http://dx.doi.org/10.5487/TR.2014.30.3.211 |
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author | Jeong, Min Ho Yang, Kwangmo Lee, Chang Geun Jeong, Dong Hyeok Park, You Soo Choi, Yoo Jin Kim, Joong Sun Oh, Su Jung Jeong, Soo Kyung Jo, Wol Soon |
author_facet | Jeong, Min Ho Yang, Kwangmo Lee, Chang Geun Jeong, Dong Hyeok Park, You Soo Choi, Yoo Jin Kim, Joong Sun Oh, Su Jung Jeong, Soo Kyung Jo, Wol Soon |
author_sort | Jeong, Min Ho |
collection | PubMed |
description | Resveratrol has received considerable attention as a polyphenol with various biological effects such as anti-inflammatory, anti-oxidant, anti-mutagenic, anti-carcinogenic, and cardioprotective properties. As part of the overall safety assessment of HS-1793, a novel resveratrol analogue free from the restriction of metabolic instability and the high dose requirement of resveratrol, we assessed genotoxicity in three in vitro assays: a bacterial mutation assay, a comet assay, and a chromosomal aberration assay. In the bacterial reverse mutation assay, HS-1793 did not increase revertant colony numbers in S. typhimurium strains (TA98, TA100, TA1535 and TA1537) or an E. coli strain (WP2 uvrA) regardless of metabolic activation. HS-1793 showed no evidence of genotoxic activity such as DNA damage on L5178Y Tk(+/−) mouse lymphoma cells with or without the S9 mix in the in vitro comet assay. No statistically significant differences in the incidence of chromosomal aberrations following HS-1793 treatment was observed on Chinese hamster lung cells exposed with or without the S9 mix. These results provide additional evidence that HS-1793 is non-genotoxic at the dose tested in three standard tests and further supports the generally recognized as safe determination of HS-1793 during early drug development. |
format | Online Article Text |
id | pubmed-4206749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Society Of Toxicology |
record_format | MEDLINE/PubMed |
spelling | pubmed-42067492014-10-23 In Vitro Genotoxicity Assessment of a Novel Resveratrol Analogue, HS-1793 Jeong, Min Ho Yang, Kwangmo Lee, Chang Geun Jeong, Dong Hyeok Park, You Soo Choi, Yoo Jin Kim, Joong Sun Oh, Su Jung Jeong, Soo Kyung Jo, Wol Soon Toxicol Res Articles Resveratrol has received considerable attention as a polyphenol with various biological effects such as anti-inflammatory, anti-oxidant, anti-mutagenic, anti-carcinogenic, and cardioprotective properties. As part of the overall safety assessment of HS-1793, a novel resveratrol analogue free from the restriction of metabolic instability and the high dose requirement of resveratrol, we assessed genotoxicity in three in vitro assays: a bacterial mutation assay, a comet assay, and a chromosomal aberration assay. In the bacterial reverse mutation assay, HS-1793 did not increase revertant colony numbers in S. typhimurium strains (TA98, TA100, TA1535 and TA1537) or an E. coli strain (WP2 uvrA) regardless of metabolic activation. HS-1793 showed no evidence of genotoxic activity such as DNA damage on L5178Y Tk(+/−) mouse lymphoma cells with or without the S9 mix in the in vitro comet assay. No statistically significant differences in the incidence of chromosomal aberrations following HS-1793 treatment was observed on Chinese hamster lung cells exposed with or without the S9 mix. These results provide additional evidence that HS-1793 is non-genotoxic at the dose tested in three standard tests and further supports the generally recognized as safe determination of HS-1793 during early drug development. The Korean Society Of Toxicology 2014-09 /pmc/articles/PMC4206749/ /pubmed/25343016 http://dx.doi.org/10.5487/TR.2014.30.3.211 Text en Copyright © 2014, The Korean Society Of Toxicology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Jeong, Min Ho Yang, Kwangmo Lee, Chang Geun Jeong, Dong Hyeok Park, You Soo Choi, Yoo Jin Kim, Joong Sun Oh, Su Jung Jeong, Soo Kyung Jo, Wol Soon In Vitro Genotoxicity Assessment of a Novel Resveratrol Analogue, HS-1793 |
title | In Vitro Genotoxicity Assessment of a Novel Resveratrol Analogue, HS-1793 |
title_full | In Vitro Genotoxicity Assessment of a Novel Resveratrol Analogue, HS-1793 |
title_fullStr | In Vitro Genotoxicity Assessment of a Novel Resveratrol Analogue, HS-1793 |
title_full_unstemmed | In Vitro Genotoxicity Assessment of a Novel Resveratrol Analogue, HS-1793 |
title_short | In Vitro Genotoxicity Assessment of a Novel Resveratrol Analogue, HS-1793 |
title_sort | in vitro genotoxicity assessment of a novel resveratrol analogue, hs-1793 |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206749/ https://www.ncbi.nlm.nih.gov/pubmed/25343016 http://dx.doi.org/10.5487/TR.2014.30.3.211 |
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