Integrative Biology Research Unit, Department of Life Sciences, Presidency University, West Bengal, India.
Department of Zoology, Visva Bharati University, Bolpur, West Bengal, India.
Sci Total Environ. 2022 Jul 15;830:154796. doi: 10.1016/j.scitotenv.2022.154796. Epub 2022 Mar 25.
Many studies have investigated the negative impacts of microplastics on teleost fishes with very little or no evidence of their mechanism of action. This scenario entreats us to investigate the toxicities of nanopolystyrene in zebrafish oocyte with emphasis on the mechanism of action. In the present study, the cellular levels of mRNA transcripts of different genetic markers (such as: sod, gpx, nrf2, inos, ucp2, and atp6 (redox-sensitive markers); nfkβ, tnfα, il-10, ikβ, gdf9, and bmp15 (immune markers); gadd45, rad51, p53 and bcl2 (DNA damage and apoptotic)) have been quantified by real-time PCR after 6 h of incubation of isolated oocyte with different doses of nanopolystyrene viz. P0 (control i.e. no polystyrene in culture medium), P1 (100 ng/ml), and P2 (400 ng/ml). Results showed that both the treatment concentrations of nanopolystyrene induce oxidative stress with % DPPH = 30.75, 31.61, and 32.43% for P0, P1, and P2, respectively. Increase in oxidative stress in oocytes with increasing doses of nanopolystyrene was also observed in TBARS assay with MDA content 0.12 and 0.21 μM for P1 and P2, respectively as compaired to the control 0.08 μM. This increased oxidative stress can regulate the expression pattern (upregulation/downregulation) of selected genes leading to different toxic effects like - oxidative stress, immunotoxicity, and apoptosis in oocytes, which suggests the impairment of reproductive functions by nanopolystyrene.
许多研究已经调查了微塑料对硬骨鱼类的负面影响,但几乎没有或没有证据表明它们的作用机制。这种情况促使我们研究纳米聚苯乙烯对斑马鱼卵母细胞的毒性,重点研究其作用机制。在本研究中,通过实时 PCR 定量了不同遗传标记物(如 sod、gpx、nrf2、inos、ucp2 和 atp6(氧化还原敏感标记物);nfkβ、tnfα、il-10、ikβ、gdf9 和 bmp15(免疫标记物);gadd45、rad51、p53 和 bcl2(DNA 损伤和凋亡))的 mRNA 转录物在不同剂量的纳米聚苯乙烯孵育 6 小时后在分离的卵母细胞中的细胞水平。结果表明,两种处理浓度的纳米聚苯乙烯都诱导了氧化应激,DPPH%分别为 30.75、31.61 和 32.43%,用于 P0(即培养基中无聚苯乙烯)、P1(100ng/ml)和 P2(400ng/ml)。随着纳米聚苯乙烯剂量的增加,TBARS 测定法也观察到卵母细胞中的氧化应激增加,MDA 含量分别为 P1 和 P2 的 0.12 和 0.21 μM,而对照为 0.08 μM。这种增加的氧化应激可以调节选定基因的表达模式(上调/下调),导致卵母细胞中的不同毒性效应,如氧化应激、免疫毒性和细胞凋亡,这表明纳米聚苯乙烯对生殖功能的损害。