Department of Zoology, Visva-Bharati, Santiniketan, 731235, West Bengal, India.
UGC-DAE Consortium for Scientific Research, Kolkata Centre, 3/LB-8, Bidhan Nagar, Kolkata, 700098, West Bengal, India.
Aquat Toxicol. 2019 Aug;213:105219. doi: 10.1016/j.aquatox.2019.06.002. Epub 2019 Jun 3.
Nrf2 is a crucial transcription factor that regulates the expression of cytoprotective enzymes and controls cellular redox homeostasis. Both arsenic and fluoride are potent toxicants that are known to induce Nrf2. They are reported to coexist in many areas of the world leading to complex mixture effects in exposed organisms. The present study investigated the expression of Nrf2 and related xenobiotic metabolizing enzymes along with other stress markers such as histopathological alterations, catalase activity, reduced glutathione content and lipid peroxidation in zebrafish liver as a function of combined exposure to environmentally relevant concentrations of arsenic (37.87 μgL or 5.05 × 10 M) and fluoride (6.8 mg L or 3.57 × 10 M) for 60 days. The decrease in the total reduced glutathione level was evident in all treatment conditions. Hyperactivity of catalase along with conspicuous elevation in reactive oxygen species, malondialdehyde content and histo-architectural anomalies signified the presence of oxidative stress in the treatment groups. Nrf2 was seen to be induced at both transcriptional and translational levels in case of both individual and co-exposure. The same pattern was observed in case of its nuclear translocation also. From the results of qRT-PCR it was evident that at each time point co-exposure to arsenic and fluoride seemed to alter the gene expression of Cu/Zn Sod, Mn Sod, Gpx and Nqo1 just like their individual exposure but at a very low magnitude. In conclusion, this study demonstrates for the first time the differential expression and activity of Nrf2 and other stress response genes in the zebrafish liver following individual and combined exposure to arsenic and fluoride.
Nrf2 是一种关键的转录因子,可调节细胞保护酶的表达并控制细胞内氧化还原稳态。砷和氟都是强有力的毒物,已知会诱导 Nrf2。据报道,它们在世界许多地区共存,导致暴露于其中的生物体产生复杂的混合效应。本研究调查了 Nrf2 及其相关的外源代谢酶的表达,以及其他应激标志物(如组织病理学改变、过氧化氢酶活性、还原型谷胱甘肽含量和脂质过氧化),作为斑马鱼肝中同时暴露于环境相关浓度砷(37.87 µgL 或 5.05×10 M)和氟(6.8 mg L 或 3.57×10 M)60 天的功能。所有处理条件下总还原型谷胱甘肽水平均明显降低。过氧化氢酶的过度活跃,以及活性氧、丙二醛含量和组织形态结构异常的显著升高,表明处理组存在氧化应激。在个体和共同暴露的情况下,Nrf2 在转录和翻译水平上均被诱导。其核易位也观察到相同的模式。从 qRT-PCR 的结果可以明显看出,在每个时间点,砷和氟的共同暴露似乎都改变了 Cu/Zn Sod、Mn Sod、Gpx 和 Nqo1 的基因表达,就像它们的单独暴露一样,但幅度非常低。总之,这项研究首次证明了 Nrf2 和其他应激反应基因在斑马鱼肝中对砷和氟的单独和联合暴露的差异表达和活性。