Modulation of radiation-induced and mitomycin C-induced chromosome damage by apigenin in human lymphocytes in vitro

被引:24
|
作者
Sharma, Narinder K. [1 ]
机构
[1] Bhabha Atom Res Ctr, Genet Toxicol & Chromosome Studies Sect, Radiat Biol & Hlth Sci Div, Bombay 400085, Maharashtra, India
关键词
Radiation; chromosomal aberration; cytochalasin-B blocked micronuclei; sister chromatid exchange; mitomycin C; antimutagenic; apigenin; CELL-CYCLE; MICRONUCLEUS TECHNIQUE; THERAPEUTIC AGENTS; OXIDATIVE STRESS; CARCINOMA-CELLS; FLAVONOIDS; DNA; GENOTOXICITY; QUERCETIN; INDUCTION;
D O I
10.1093/jrr/rrs117
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Apigenin (APG), a flavone, is known to exhibit antioxidant, antimutagenic and antitumorigenic activity, both in vivo and in vitro. The aim of this study is to investigate the modulatory effects of APG on human lymphocytes after irradiation with gamma rays (3 Gy) or treatment with the antineoplastic agent, mitomycin C (MMC), in vitro. Cytogenetic biomarkers such as chromosome aberrations (CAs), sister chromatid exchanges (SCEs) and cytochalasin-B blocked micronuclei (CBMN), were studied in blood lymphocytes treated with radiation, or antineoplastic agent (MMC), and APG. Whole blood lymphocytes were cultured in vitro using a standard protocol. No significant differences were found in the frequency of CAs or micronuclei (MN) in human peripheral blood lymphocytes irradiated with gamma rays (3 Gy) and then post-treated with APG. There was an increase in the frequency of SCEs per cell in APG-treated samples compared with the controls. Lymphocytes treated with MMC in the presence of APG exhibited a significant decrease (P < 0.01) in the frequency of SCEs compared with MMC treatment alone. The data for the MN test indicated that APG treatment significantly reduced (P < 0.01) the frequency of MMC-induced MN.
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页码:789 / 797
页数:9
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