Sarkar Shuvasree, Mukherjee Sandip, Chattopadhyay Ansuman, Bhattacharya Shelley
Environmental Toxicology Laboratory, Department of Zoology, School of Life Science, Visva-Bharati University, Santiniketan, West Bengal 731235, India.
Radiation Genetics and Chemical Mutagenesis Laboratory, Department of Zoology, School of Life Science, Visva-Bharati University, Santiniketan, West Bengal 731235, India.
Ecotoxicol Environ Saf. 2014 Sep;107:1-8. doi: 10.1016/j.ecoenv.2014.05.012. Epub 2014 Jun 3.
Occurrence of arsenic in the aquatic environment of West Bengal (India), Bangladesh and other countries are of immediate environmental concern. In the present study, zebrafish (Danio rerio) was used as a model to investigate oxidative stress related enzyme activities and expression of antioxidant genes in the brain to 50µg/L arsenic trioxide for 90 days. In treated fish, generation of reactive oxygen species (ROS), malondialdehyde (MDA) and conjugated diene (CD) showed a triphasic response attaining a peak at the end of the exposure. In addition, a gradual increase in GSH level was noted until 60 days and at 90 days, a sudden fall was recorded which heightened arsenic toxicity. However, GSH level does not correlate well with the glutathione reductase (GR) activity. Generation of ROS in zebrafish brain due to As2O3 exposure was further evidenced by significant alteration of glutathione peroxidase (GPx) and catalase (CAT) activity, which converts H2O2 to water and helps in detoxication. Moreover, enhanced mRNA level of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) in As2O3 exposed zebrafish indicates a protective role of Nrf2. kelch-like ECH-associated protein 1 (Keap1), a negative regulator of Nrf2, inversely correlates with the mRNA expression of Nrf2. As2O3 induced toxicity was also validated by the alteration in NRF2 and NRF2 dependent expression of proteins such as heme oxygenase1 (HO1) and NAD(P)H dehydrogenase quinone1 (NQO1). The mRNA expression of glutathione peroxidase (Gpx1), catalase (Cat), manganese superoxide dismutase (Mn-Sod), copper/zinc superoxide dismutase (Cu/Zn Sod) and cytochrome c oxidase1 (Cox1) were also up regulated. The expression of uncoupling protein 2 (Ucp2), an important mitochondrial enzyme was also subdued in arsenic exposed zebrafish. The oxidative stress induced by arsenic also cause reduced mRNA expression of B-cell lymphoma 2 (Bcl2) present in the inner mitochondrial membrane and thereby indicating onset of apoptosis in treated fish. It is concluded that even a low dose of arsenic trioxide is toxic enough to induce significant oxidative stress in zebrafish brain.
印度西孟加拉邦、孟加拉国及其他国家水生环境中砷的存在引发了人们对环境的直接关注。在本研究中,斑马鱼(Danio rerio)被用作模型,以研究其暴露于50µg/L三氧化二砷90天后,大脑中与氧化应激相关的酶活性及抗氧化基因的表达情况。在经处理的斑马鱼中,活性氧(ROS)、丙二醛(MDA)和共轭二烯(CD)的生成呈现出三相反应,在暴露结束时达到峰值。此外,谷胱甘肽(GSH)水平在60天前逐渐升高,而在90天时突然下降,这加剧了砷的毒性。然而,GSH水平与谷胱甘肽还原酶(GR)活性的相关性不佳。三氧化二砷暴露导致斑马鱼大脑中ROS的生成,这进一步通过谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT)活性的显著变化得到证实,这些酶将过氧化氢转化为水并有助于解毒。此外,暴露于三氧化二砷的斑马鱼中核因子(红系衍生2)样2(Nrf2)的mRNA水平升高,表明Nrf2具有保护作用。kelch样ECH相关蛋白1(Keap1)作为Nrf2的负调节因子,与Nrf2的mRNA表达呈负相关。三氧化二砷诱导的毒性还通过NRF2以及NRF2依赖性蛋白如血红素加氧酶1(HO1)和NAD(P)H脱氢酶醌1(NQO1)表达的改变得到验证。谷胱甘肽过氧化物酶(Gpx1)、过氧化氢酶(Cat)、锰超氧化物歧化酶(Mn-Sod)、铜/锌超氧化物歧化酶(Cu/Zn Sod)和细胞色素c氧化酶1(Cox1)的mRNA表达也上调。解偶联蛋白2(Ucp2)作为一种重要的线粒体酶,其表达在暴露于砷的斑马鱼中也受到抑制。砷诱导的氧化应激还导致线粒体内膜中存在的B细胞淋巴瘤2(Bcl2)的mRNA表达降低,从而表明经处理的斑马鱼开始出现凋亡。研究得出结论,即使是低剂量的三氧化二砷也具有足够毒性,可在斑马鱼大脑中诱导显著的氧化应激。