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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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Detalles Bibliográficos
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
Descripción
Sumario: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.