ABSTRACT
【Objective】 To compare PC-12 cells’ apoptosis caused by the serotonin herbicides atrazine （ATR）， simazine （SIM） and cyanazine （CYA）. 【Methods】 The rat adrenal medullary pheochromoma PC-12 cell line was selected for routine culture. At the cell logarithmic growth phase， ATR， SIM and CYA were used at a concentration of 200 μmol/L for 24 h， respectively， and the same solvent was added in the control group. The CCK-8 method was used to detect the cell survival rate； the content of reactive oxygen species （ROS） in PC-12 cells was detected； the Real-time PCR and Western blotting methods were used to detect the mRNA and protein expressions of Bax， p53， Bcl-2 and Caspase-3. 【Results】 Compared with that in the control group， the survival rate of the cells in ATR group， SIM group and CYA group was significantly decreased. The intracellular ROS activity of the three groups was significantly increased， and the mRNA and protein expressions of Bax， p53 and Caspase-3 were increased. mRNA and protein expressions of Bcl-2 were significantly reduced （P<0.01）. Compared with that in ATR group， the cell survival rate of SIM group and CYA group was significantly increased， the intracellular ROS activity of the two groups was significantly decreased， the expressions of Bax， p53 and Caspase-3 mRNA and protein were significantly reduced， and the expressions of Bcl-2 mRNA and protein were significantly increased （P<0.01）. Compared with that of SIM group， the cell survival rate of CYA group was significantly increased， while the intracellular ROS activity was significantly decreased； the Bax， p53 and Caspase-3 mRNA and protein expressions were significantly reduced， and Bcl-2 mRNA and protein expressions were significantly increased （P<0.01）. 【Conclusion】 ATR， SIM and CYA can all promote PC-12 cells’ apoptosis； ATR has the strongest effect while CYA has the weakest effect.
ABSTRACT
Aim: To identify the oxidative stress impacts of chloro-s-triazine herbicides on human mammary epithelial cell lines.Study Design:MCF-7 mammary epithelial carcinoma and MCF-10A mammary epithelial cells were treated with levels of three triazine herbicides in concentrations flanking the US FDA safe levels. Place and Duration of Study:Department of Biology, Millikin University, in January 2015 through December 2015 and January 2019 through May 2020.Methodology:We examined the oxidative effects of two triazine herbicides, atrazine and simazine, on estrogen-dependent MCF-7 mammary epithelial carcinoma cells using three different bioluminescent assay techniques. We then utilized real time PCR to analyze gene expression through RT-PCR analysis, in both MCF-7 cells and a non-cancerous cell line, MCF-10A, for both of these triazine herbicides plus the related cyanazine.Results:At all concentrations of atrazine and simazine, no statistical differences were found in the levels of oxidized glutathione or total oxidized and reduced nicotinamide adenine dinucleotides phosphates. In stark contrast, levels of hydrogen peroxide were found tobe statistically different from the control at all concentrations of atrazine and simazine tested. Using an Analysis of Variance (ANOVA) we determined that within the enzymatic portion of the hydrogen peroxide pathway there were statistically significant differences in the expression of Peroxiredoxin 1 (PRDX1), Sulfiredoxin (SRXN1), and Thioredoxin (TXN).Conclusion:Exposure to triazines alters the hydrogen peroxide pathway, which in turn can greatly affect the stability of the cell milieu