Zwolak Iwona, Zaporowska Halina
Department of Cell Biology, Institute of Environmental Protection, John Paul II Catholic University of Lublin, Lublin, Poland.
Acta Biol Hung. 2009 Mar;60(1):55-67. doi: 10.1556/ABiol.60.2009.1.6.
In the present work, we investigated the cytotoxicity of vanadium and the influence of zinc and selenium on vanadium-dependent cell damage in the BALB/c 3T3 cell culture. Treatment of cells for 24 hours with medium containing 50, 100 and 200 microM NaVO3 caused a significant decrease in the cell viability as measured by MTT test. Furthermore, the assays for reactive oxygen species (NBT reduction and phenol red oxidation) demonstrated the increase in superoxide and hydrogen peroxide production. In the cotreatment studies, the cells were exposed to NaVO3 (50, 100 and 200 microM) in the presence of nontoxic concentrations of ZnCl2 (5 microM) or Na2SeO3 (0.5 microM). Following 24 h incubation, the cell viability (assessed in MTT assay) and reactive oxygen species generation were evaluated. Our data suggest that zinc and selenium, in the concentrations mentioned above, provide no protection against adverse actions induced by sodium metavanadate at concentration levels of 50, 100 and 200 microM. To our knowledge, this is the first report from in vitro studies on interaction between pentavalent vanadium and trace elements that function as antioxidants: zinc and selenium.
在本研究中,我们研究了钒的细胞毒性以及锌和硒对BALB/c 3T3细胞培养中钒依赖性细胞损伤的影响。用含有50、100和200微摩尔偏钒酸钠的培养基处理细胞24小时,通过MTT试验测定,细胞活力显著降低。此外,活性氧检测(NBT还原和酚红氧化)表明超氧化物和过氧化氢生成增加。在联合处理研究中,细胞在无毒浓度的氯化锌(5微摩尔)或亚硒酸钠(0.5微摩尔)存在下暴露于偏钒酸钠(50、100和200微摩尔)。孵育24小时后,评估细胞活力(通过MTT试验评估)和活性氧生成。我们的数据表明,上述浓度的锌和硒不能保护细胞免受50、100和200微摩尔浓度的偏钒酸钠诱导的不良作用。据我们所知,这是关于五价钒与作为抗氧化剂的微量元素锌和硒之间相互作用的体外研究的首次报道。