Please use this identifier to cite or link to this item: http://repositorio.ufc.br/handle/riufc/5542
Type: Artigo de Periódico
Title: 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
Authors: Cavalcanti, Bruno C.
Ferreira, José R. O.
Cabral, Igor O.
Magalhães, Hemerson I. F.
Oliveira, Cecília C. de
Rodrigues, Felipe A. R.
Rocha, Danilo D.
Barros, Francisco W. A.
Silva, Cecília R. da
Nobre Júnior, Hélio Vitoriano
Canuto, Kirley Marques
Silveira, Edilberto R.
Pessoa, Cláudia
Moraes Filho, Manoel Odorico de
Keywords: Quimioprevenção;Leucócitos
Issue Date: Nov-2012
Publisher: Food and Chemical Toxicology
Citation: CAVALCANTI, B. C. et al. Genetic toxicology evaluation of essential oil of Alpinia zerumbet and its chemoprotective effects against H2O2 -induced DNA damage in cultured human leukocytes. Food and Chemical Toxicology, Oxford, v. 50, n. 11, p. 4051-4061, nov. 2012.
Abstract: Essential oil (EO) of Alpinia zerumbet leaves, at non-toxic concentrations (50–300 l g/mL), did not induce genotoxicity in human leukocytes. However, at the highest concentration (500 l g/mL) tested caused a reduction in cell proliferation and viability, and an increase in DNA damage. Moreover, in vivo experi- ments showed that EO (400 mg/kg) did not exert mutagenicity on peripheral blood cells and bone mar- row 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 cul- tures exposed to 500 l g/mL EO. In conclusion, EO at concentrations up to 300 l g/mL or doses up to 400 mg/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
URI: http://www.repositorio.ufc.br/handle/riufc/5542
ISSN: 0278-6915
Appears in Collections:DMC - Artigos publicados em revistas científicas

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