Department of General and Environmental Microbiology, Faculty of Sciences, University of Pécs, P.O. Box 266, Pécs H-7602, Hungary.
Toxicon. 2013 Oct;73:130-43. doi: 10.1016/j.toxicon.2013.07.015. Epub 2013 Jul 27.
This study investigates the non-estrogenic mode of zearalenone (ZEA) toxicity in a novel aspect via accumulation of reactive oxygen species (ROS) and the regulation of the activities of antioxidant enzymes in the Schizosaccharomyces pombe in acute toxicity tests. In comparison with the control, 500 μM ZEA treatment caused 66% decrease in the concentration of glutathione (GSH), which was a consequence, in the absence of ZEA-GSH interaction, of the GSH-consuming processes of the antioxidant system; this depletion of GSH initiated a 1.8- and 2.0-fold accumulation of the superoxide anion and hydrogen peroxide, but did not increase the concentration of the hydroxyl radical; ROS-induced adaptation processes via activation of the Pap1 transcription factor resulted in significantly increased activities of superoxide dismutases, catalase, glutathione reductase and glutathione S-transferase, and decreased activities of glutathione peroxidase and glucose-6-phosphate dehydrogenase. This treatment altered the sterol composition of the cells by inducing decreased concentrations of ergosterol, squalene and 24-methylene-24,25-hydrolanosterol, and also elevated the number of fragmented nuclei. Cells strived to correct the unbalanced redox state by regulation of the antioxidant system, but this was not enough to defend the cells from the disturbed sterol composition, the cell cycle arrest, and the fragmentation of nuclei.
本研究通过在急性毒性试验中检测秀丽隐杆酵母中活性氧 (ROS) 的积累和抗氧化酶活性的变化,从一个新的角度研究了玉米赤霉烯酮 (ZEA) 的非雌激素毒性作用模式。与对照组相比,500μM ZEA 处理导致谷胱甘肽 (GSH) 浓度降低 66%,这是由于抗氧化系统的 GSH 消耗过程中缺乏 ZEA-GSH 相互作用;GSH 的耗竭引发了超氧阴离子和过氧化氢分别积累 1.8 倍和 2.0 倍,但没有增加羟自由基的浓度;ROS 通过激活转录因子 Pap1 诱导的适应过程导致超氧化物歧化酶、过氧化氢酶、谷胱甘肽还原酶和谷胱甘肽 S-转移酶的活性显著增加,而谷胱甘肽过氧化物酶和葡萄糖-6-磷酸脱氢酶的活性降低。这种处理通过诱导麦角固醇、角鲨烯和 24-亚甲基-24,25-羊毛甾醇浓度降低来改变细胞的甾醇组成,同时还增加了碎片化核的数量。细胞通过调节抗氧化系统来努力纠正失衡的氧化还原状态,但这不足以保护细胞免受紊乱的甾醇组成、细胞周期停滞和核碎片化的影响。