Ryu, Jae-Chun Kim, Youn-Jung Kim, Mi-Soon Kim, Min-Ji Sarma, Sailendra Nath Lee, Seung-Ho 2024-01-21T04:13:17Z 2024-01-21T04:13:17Z 2022-01-11 2005-09-30 1738-642X https://pubs.kist.re.kr/handle/201004/136111 21 alpha- and beta-Methylmelianodiol were isolated as the inhibitor of IL-5 bioactivity from Poncirus tripoliata. To develope as an anti-septic drug, the genotoxicity of 21 alpha- and beta-methyimelianodiol was subjected to high throughput toxicity screening (HTTS) because they revealed strong IL-5 inhibitory activity and limitation of quantity. Mouse lymphoma thymidine kinase (tk(+/-)) gene assay (MOLY), single cell gel electrophoresis (Comet) assay in mammalian cells and Ames reverse mutation assay in bacterial system were used as simplified, inexpensive, short-term in vitro screening tests in our laboratory. These compounds are not mutagenic in S. typhimurium TA98 and TA100 strains both in the presence and absence of metabolic activation. Before performing the comet assay, IC20 of 21 alpha-methylmelianodiol was determined the concentration of 25.51 mu g/mL and 21.99 mu g/mL with and without S-9, respectively. Also 21 beta-methylmelianodiol was determined the concentration of 24.15 mu g/mL and 22.46 mu g/mL with and without S-9, respectively. In the comet assay, DNA damage was not observed both 21 alpha-methylmelianodiol and 21 alpha-methylmelianodiol in mouse lymphoma cell line. Also, the mutant frequencies in the treated cultures were similar to the vehicle controls, and none of 21 alpha- and beta-methylmelianodiol with and without S-9 doses induced a mutant frequency over twice the background. It is suggests that 21 alpha- and beta-methylmelianodiol are non-mutagenic in MOLY assay. The results of this battery of assays indicate that 21 alpha- and beta-methylmelianodiol have no genotoxic potential in bacterial or mammalian cell systems. Therefore, we suggest that 21 alpha- and beta-methylmelianodiol, as the optimal candidates with both no genotoxic potential and IL-5 inhibitory effects must be chosen. English KOREAN SOC TOXICOGENOMICS & TOXICOPROTEOMICS MUTAGENICITY TEST FRUIT EXTRACT DNA-DAMAGE IN-VITRO CARCINOGENS ASSAY Genotoxicity on 21a-and beta-methylmelianodiol, a component of Poncirus trifoliata, in bacterial and mammalian cells Article 1 MOLECULAR & CELLULAR TOXICOLOGY, v.1, no.3, pp.172 - 178 MOLECULAR & CELLULAR TOXICOLOGY 1 3 172 178 scie 000243595800005 Biochemistry & Molecular Biology Toxicology Biochemistry & Molecular Biology Toxicology Article MUTAGENICITY TEST FRUIT EXTRACT DNA-DAMAGE IN-VITRO CARCINOGENS ASSAY 21 alpha- and beta-Methylmelianodiol Poncirus tripoliata genotoxicity MOLY comet assay Ames reverse mutation assay IL-5 inhibitory effects