201. Genetic toxicology evaluation of essential oil of Alpinia zerumbet and its chemoprotective effects against H(2)O(2)-induced DNA damage in cultured human leukocytes
- Author
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Edilberto R. Silveira, Francisco W.A. Barros, Manoel Odorico de Moraes, Kirley Marques Canuto, Danilo D. Rocha, Bruno C. Cavalcanti, Cecília C. de Oliveira, Hemerson Iury Ferreira Magalhães, Felipe A. R. Rodrigues, José Roberto de Oliveira Ferreira, Hélio Vitoriano Nobre Júnior, Cláudia Pessoa, Cecília Rocha da Silva, and Igor O. Cabral
- Subjects
Male ,DNA damage ,DPPH ,Apoptosis ,Toxicology ,medicine.disease_cause ,Protective Agents ,Antioxidants ,Gas Chromatography-Mass Spectrometry ,Lipid peroxidation ,chemistry.chemical_compound ,Mice ,medicine ,Leukocytes ,Oils, Volatile ,Alpinia zerumbet ,Animals ,Humans ,chemistry.chemical_classification ,Chromosome Aberrations ,Reactive oxygen species ,Micronucleus Tests ,biology ,Mutagenicity Tests ,General Medicine ,Glutathione ,Free Radical Scavengers ,Hydrogen Peroxide ,biology.organism_classification ,Molecular biology ,chemistry ,Biochemistry ,Micronucleus test ,Alpinia ,Female ,Lipid Peroxidation ,Reactive Oxygen Species ,Genotoxicity ,Food Science ,DNA Damage - Abstract
Essential oil (EO) of Alpinia zerumbet leaves, at non-toxic concentrations (50-300 μg/mL), did not induce genotoxicity in human leukocytes. However, at the highest concentration (500 μg/mL) tested caused a reduction in cell proliferation and viability, and an increase in DNA damage. Moreover, in vivo experiments showed that EO (400 mg/kg) did not exert mutagenicity on peripheral blood cells and bone marrow in mice. In DPPH test, EO showed scavenging effects against DPPH radicals, and other free radicals (determination of intracellular GSH and lipid peroxidation assays). Furthermore, EO was able to reduce the intracellular levels of ROS, and prevented leukocytes DNA against oxidative damage. The ability of EO to reduce H(2)O(2) toxicity was observed only when cells were treated with EO during and after exposure to H(2)O(2). With the co- and post-treatment procedures, EO decreased the frequency of apoptotic and micronucleated leukocytes as well DNA strand breaks. However, a synergistic effect was observed in cultures exposed to 500 μg/mL EO. In conclusion, EO at concentrations up to 300 μg/mL or doses up to 400mg/kg are not mutagenic in leukocytes and in mice, but do have antioxidative and protective effects against the cytotoxicity and clastogenesis induced by H(2)O(2).
- Published
- 2011