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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society Of Toxicology 2014
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.
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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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