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Iodoacetic acid disrupts mouse oocyte maturation by inducing oxidative stress and spindle abnormalities

机译:碘乙酸通过诱导氧化应激和主轴异常来破坏小鼠卵母细胞成熟

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Disinfection by-products (DBPs) are compounds produced during the water disinfection process. Iodoacetic acid (IAA) is one of the unregulated DBPs in drinking water, with potent cytotoxicity and genotoxicity in animals. However, whether IAA has toxic effects on oocyte maturation remains unclear. Here, we show that IAA exposure resulted in metaphase I (MI) arrest and polar-body-extrusion failure in mouse oocytes, indicating that IAA had adverse effects on mouse oocyte maturation in vitro. Particularly, IAA treatment caused abnormal spindle assembly and chromosome misalignment. Previous studies reported that IAA is a known inducer of oxidative stress in non-germline cells. Correspondingly, we found that IAA exposure increased the reactive oxygen species (ROS) levels in oocytes in a dose-dependent manner, indicating IAA exposure could induce oxidative stress in oocytes. Simultaneously, DNA damage was also elevated in the nuclei of these IAA-exposed mouse oocytes, evidenced by increased gamma-H2AX focus number. In addition, the un-arrested oocytes entered metaphase II (MII) with severe defects in spindle morphologies and chromosome alignment after 14-h IAA treatment. An antioxidant, N-acetyl-L-cysteine (NAC), reduced the elevated ROS level and restored the meiotic maturation in the IAA-exposed oocytes, which indicates that IAA-induced maturation failure in oocytes was mainly mediated by oxidative stress. Collectively, our results indicate that IAA exposure interfered with mouse oocyte maturation by elevating ROS levels, disrupting spindle assembly, inducing DNA damage, and causing MI arrest. Published by Elsevier Ltd.
机译:消毒副产品(DBPS)是在水消毒过程中产生的化合物。碘乙酸(IAA)是饮用水中未调节的DBPS之一,具有有效的细胞毒性和动物遗传毒性。然而,IAA是否对卵母细胞成熟具有毒性作用仍不清楚。在这里,我们表明,IAA暴露导致小鼠卵母细胞中的中期I(MI)停滞和偏光体挤出失效,表明IAA对体外对小鼠卵母细胞成熟产生不利影响。特别是,IAA治疗引起了主轴组件异常和染色体未对准。以前的研究报道说,IAA是非系列细胞中氧化应激的已知诱导剂。相应地,我们发现IAA暴露以剂量依赖性方式增加卵母细胞中的活性氧物质(ROS)水平,表明IAA暴露可以诱导卵母细胞中的氧化应激。同时,在这些暴露的小鼠卵母细胞的细胞核中也升高了DNA损伤,通过增加的γ-H2AX焦点证明。此外,未被捕获的卵母细胞进入中期II(MII),在14-H IAA治疗后的主轴形态和染色体对准中具有严重缺陷。抗氧化剂,N-乙酰-1-半胱氨酸(NAC),降低升高的ROS水平并恢复了IAA暴露的卵母细胞中的减数分裂成熟,这表明IAA诱导的卵母细胞的成熟失败主要是通过氧化应激介导的。统称,我们的结果表明IAA暴露通过升高ROS水平,扰乱主轴组件,诱导DNA损伤并导致MI骤停而受到小鼠卵母细胞成熟。 elsevier有限公司出版

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