Genetic toxicology evaluation of essential oil of Alpinia zerumbet and its chemoprotective effects against H2O2-induced DNA damage in cultured human leukocytes

被引:34
作者
Cavalcanti, Bruno C. [1 ]
Ferreira, Jose R. O. [1 ]
Cabral, Igor O. [1 ]
Magalhaes, Hemerson I. F. [1 ]
de Oliveira, Cecilia C. [1 ]
Rodrigues, Felipe A. R. [1 ]
Rocha, Danilo D. [1 ]
Barros, Francisco W. A. [1 ]
da Silva, Cecilia R. [2 ]
Junior, Helio V. N. [2 ]
Canuto, Kirley M. [3 ]
Silveira, Edilberto R. [1 ,4 ]
Pessoa, Claudia [1 ]
Moraes, Manoel O. [1 ]
机构
[1] Univ Fed Ceara, Dept Physiol & Pharmacol, Natl Lab Expt Oncol, BR-60430270 Fortaleza, Ceara, Brazil
[2] Univ Fed Ceara, Dept Clin & Toxicol Anal, BR-60430270 Fortaleza, Ceara, Brazil
[3] Embrapa Trop Agroind, BR-60511110 Fortaleza, Ceara, Brazil
[4] Univ Fed Ceara, Dept Organ & Inorgan Chem, BR-60021940 Fortaleza, Ceara, Brazil
关键词
Alpinia zerumbet; Antimutagenesis; Chemoprevention; Antioxidative actions; PERS. BL BURTT; IN-VITRO; COMET ASSAY; PHENOLIC-COMPOUNDS; OXIDATIVE STRESS; PLANT-EXTRACTS; K; SCHUM; ANTIOXIDANT; GENOTOXICITY; MONOTERPENES;
D O I
10.1016/j.fct.2012.03.038
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Essential oil (EO) of Alpinia zerumbet leaves, at non-toxic concentrations (50-300 mu g/mL), did not induce genotoxicity in human leukocytes. However, at the highest concentration (500 mu g/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 H2O2 toxicity was observed only when cells were treated with EO during and after exposure to H2O2. 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 mu g/mL EO. In conclusion, EO at concentrations up to 300 mu 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 H2O2. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4051 / 4061
页数:11
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