Journal of Agricultural and Food Chemistry · 1997 · 66 citations · 12 references
PharmacyMicrobiologyToxicologyBiochemical ToxicologyMicrobial EcologyMicrobial GeneticsGenotoxicity TestingMutagenicity AssessmentBioactivity ScreeningColumn ChromatographyFractionationN-hexane Toxicity
A methanol extract from Dendrobium nobile showed a suppressive effect on umu gene expression of the SOS response in Salmonella typhimurium TA1535/pSK1002 against the mutagen 2-(2-furyl)-3-(5-nitro-2-furyl)acrylamide (furylfuramide). The methanol extract from D. nobile was re-extracted with n -hexane, dichloromethane, 1-butanol, and water, respectively. A suppressive compound in the n -hexane extract fraction was isolated by SiO 2 column chromatography and chemical fractionation and was identified as gigantol by EI-MS and 1 H and 13 C NMR spectroscopy. Gigantol suppressed the SOS-inducing activity of furylfuramide in the umu test. Gene expression was suppressed 90% at <0.73 μmol/mL, and the ID 50 value was 0.35 μmol/mL. Gigantol was also assayed with the mutagen 3-amino-1,4-dimethyl-5 H -pyrido[4,3 b ]indole (Trp-P-1), which requires liver metabolizing enzymes, and it suppressed the SOS-inducing activity of Trp-P-1 in the umu test. Gene expression was suppressed 91% at <0.73 μmol/mL, and the ID 50 value was 0.32 μmol/mL. In addition, gigantol was assayed for suppressive effect on UV irradiation in the umu test, where it showed suppression of the SOS-inducing activity caused by UV irradiation. Gene expression was suppressed 84% at <0.36 μmol/mL, and the ID 50 value was 0.17 μmol/mL. The antimutagenic activities of gigantol against furylfuramide and Trp-P-1 were assayed by an Ames test using S. typhimurium TA100, which indicated that gigantol suppressed each of the mutagens. Keywords: Dendrobium nobile; gigantol; Orchidaceae; antimutagenic activity; umu test; Ames test
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