Laboratoire de Biochimie et Toxicologie de l'Environnement, ISA, Chott-Mariem, Sousse, Tunisie.
Arch Environ Contam Toxicol. 2010 Oct;59(3):513-9. doi: 10.1007/s00244-010-9494-5. Epub 2010 Mar 18.
Cadmium (Cd), one of the most widely distributed heavy metals, is highly toxic to humans and animals. It is well known that zinc (Zn) and selenium (Se) administration reduce the Cd-induced toxicity and that metallothioneins can have a protective effect to mitigate Cd toxicity in biological systems. In this study we report the expression analysis of the two metallothioneines gene classes MT-1 and MT-2 as well as the total metalloprotein content in the liver of rats exposed to Cd (200 ppm), Cd + Zn (200 ppm + 500 ppm), Cd + Se (200 ppm + 0.1 ppm) or Cd + Zn + Se (200 ppm + 500 ppm + 0.1 ppm) in their drinking water for 35 days. Metals accumulation was quantified in rat liver. Cd decreased significantly the hepatic concentrations of Se and increased those of Zn. The treatment of Cd-exposed rats with Se alone or combined with Zn reversed the Cd-induced depletion of Se concentrations in the liver. However, Zn or Zn + Se administration significantly increased the liver Cd uptake and had no effect on the Cd-induced increase in hepatic concentrations of Zn. The molecular assay showed a decreasing trend of MT-1 relative gene expression levels in animals supplemented with Zn (6.87-fold), Se (3.58-fold), and their combination (1.69-fold) when compared to Cd-treated animals (16.22-fold). Upregulation of the MT-2 expression were recorded in all conditions, although fold induction levels were less pronounced than MT-1 expressions. Our data suggest that the well-established protective effect of Zn and Se against Cd-induced toxicity passes through non-MT gene expression mechanisms, being more dependent on the oxidative stress status of the cell.
镉(Cd)是分布最广泛的重金属之一,对人类和动物具有高度毒性。众所周知,锌(Zn)和硒(Se)的给药可以降低 Cd 诱导的毒性,并且金属硫蛋白可以具有保护作用,以减轻生物系统中 Cd 的毒性。在这项研究中,我们报告了暴露于 Cd(200 ppm)、Cd+Zn(200 ppm+500 ppm)、Cd+Se(200 ppm+0.1 ppm)或 Cd+Zn+Se(200 ppm+500 ppm+0.1 ppm)的大鼠肝脏中两种金属硫蛋白基因类 MT-1 和 MT-2 的表达分析以及总金属蛋白含量,在饮用水中 35 天。在大鼠肝脏中定量了金属的积累。Cd 显著降低了肝脏中的 Se 浓度,并增加了 Zn 的浓度。用 Se 单独或与 Zn 联合处理 Cd 暴露的大鼠逆转了肝脏中 Se 浓度的 Cd 诱导消耗。然而,Zn 或 Zn+Se 的给药显著增加了肝脏对 Cd 的摄取,并且对 Cd 诱导的肝脏 Zn 浓度增加没有影响。分子测定显示,与 Cd 处理的动物(16.22 倍)相比,用 Zn(6.87 倍)、Se(3.58 倍)及其组合(1.69 倍)补充的动物的 MT-1 相对基因表达水平呈下降趋势。在所有条件下都记录到 MT-2 表达的上调,尽管诱导倍数低于 MT-1 表达。我们的数据表明,Zn 和 Se 对 Cd 诱导的毒性的既定保护作用是通过非 MT 基因表达机制实现的,这更依赖于细胞的氧化应激状态。