College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.
College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China; Key Laboratory of the Provincial Education Department of Heilongjiang for Common Animal Disease Prevention and Treatment, College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, PR China.
Fish Shellfish Immunol. 2022 Dec;131:1075-1084. doi: 10.1016/j.fsi.2022.11.024. Epub 2022 Nov 14.
Atrazine (ATR) is a herbicide widely used in grass crops. The pollution of the soil and water environment is extremely harmful to aquatic animals and their offspring. iNOS/NO upregulation, DNA damage and cellular autophagy affect the immune function of fish liver cells. The effects of ATR at exposure doses on grass carp hepatocytes in terms of autophagy and DNA damage effects in genotoxicity, as well as the antagonistic effects of TAN on the above phenotypes and the internal mechanisms are not known. Therefore, we constructed control (Con group), ATR exposure (ATR group), TAN exposure (TAN group) and mixed group (ATR + TAN group) models on grass carp hepatocytes. Validation was performed by comet assay, MDC staining, qRT-PCR and protein blotting assay as well as iNOS/NO indicator levels and expression of immune factors as these experimental methods. Our data indicate that iNOS/NO assay kit measured that ATR treatment resulted in a significant increase in iNOS/NO activity and levels in grass carp hepatocytes (p < 0.05). We also found that NO/iNOS/NF-κB pathway genes were significantly activated (p < 0.05) at the exposure dose of ATR (3 μg mL). In addition, the proportion of cells that died due to DNA damage, autophagy, and immunotoxic effects was significantly increased at the exposure dose of ATR. Comet assay protein blotting detected increased DNA damage in cells at the ATR exposure dose (p < 0.05). MDC staining and qRT-PCR and protein blotting to detect the proportion of autophagic cells and autophagy-related genes also appeared upregulated at the exposed dose of ATR (p < 0.05). In brief, this study showed that ATR exposure caused cellular DNA damage and autophagy via the NO/iNOS/NF-κB axis, which led to immunotoxic effects and eventual death of grass carp hepatocytes. The present study facilitates the demonstration of the molecular mechanism of TAN alleviation of ATR cytotoxicity from the perspective of NO-mediated iNOS/NF-κB axis. It provides insights into the protection of farmed fish from agricultural contaminants and opens up new horizons in the use of natural plant-derived monomers for the clinical treatment of antagonistic triazine pesticide poisoning.
莠去津(ATR)是一种广泛用于草类作物的除草剂。土壤和水环境的污染对水生动物及其后代极其有害。诱导型一氧化氮合酶/一氧化氮(iNOS/NO)上调、DNA 损伤和细胞自噬会影响鱼类肝细胞的免疫功能。ATR 在暴露剂量下对草鱼肝细胞的自噬和 DNA 损伤作用以及在遗传毒性方面的影响,以及 TAN 对上述表型和内在机制的拮抗作用尚不清楚。因此,我们构建了草鱼肝细胞的对照组(Con 组)、ATR 暴露组(ATR 组)、TAN 暴露组(TAN 组)和混合组(ATR+TAN 组)。通过彗星试验、MDC 染色、qRT-PCR 和蛋白印迹试验以及 iNOS/NO 指标水平和免疫因子的表达来验证这些实验方法。我们的数据表明,ATR 处理导致草鱼肝细胞中 iNOS/NO 活性和水平显著增加(p<0.05)。我们还发现,在 ATR 暴露剂量下(3μg mL),NO/iNOS/NF-κB 通路基因显著激活(p<0.05)。此外,在 ATR 暴露剂量下,由于 DNA 损伤、自噬和免疫毒性作用而死亡的细胞比例显著增加。彗星试验蛋白印迹检测到 ATR 暴露剂量下细胞的 DNA 损伤增加(p<0.05)。MDC 染色和 qRT-PCR 以及蛋白印迹检测自噬细胞和自噬相关基因的比例也在 ATR 暴露剂量下上调(p<0.05)。总之,本研究表明,ATR 暴露通过 NO/iNOS/NF-κB 轴导致细胞 DNA 损伤和自噬,从而导致草鱼肝细胞的免疫毒性作用和最终死亡。本研究从 NO 介导的 iNOS/NF-κB 轴的角度展示了 TAN 缓解 ATR 细胞毒性的分子机制,为保护养殖鱼类免受农业污染物的侵害提供了新的思路,并为利用天然植物衍生单体治疗拮抗三嗪类农药中毒开辟了新的前景。