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增塑剂邻苯二甲酸二(2-乙基己基)酯在体内引起减数分裂缺陷并降低小鼠卵母细胞的受精能力。

Plasticizer Bis(2-ethylhexyl) Phthalate Causes Meiosis Defects and Decreases Fertilization Ability of Mouse Oocytes in Vivo.

机构信息

College of Veterinary Medicine , Northwest A&F University , Yangling , Shaanxi Province 712100 , PR China.

Xining Animal Husbandry and Veterinary Station , Xining , Qinghai Province 810003 , PR China.

出版信息

J Agric Food Chem. 2019 Mar 27;67(12):3459-3468. doi: 10.1021/acs.jafc.9b00121. Epub 2019 Mar 12.

Abstract

Bis(2-ethylhexyl) phthalate (DEHP) is a widely used plasticizer in polyvinyl chloride (PVC) plastics. Humans and animals are widely and continuously exposed to DEHP, especially with respect to diet, which is associated with reproductive diseases. Nevertheless, the effects and underlying mechanisms of DEHP exposure on oocytes in vivo remain ambiguous. In this study, we found that oral administration of DEHP (40 μg/kg body weight per day for 14 days) markedly reduced the maturation and fertilization of oocytes in vivo. In addition, DEHP caused oxidative stress, increased reactive oxygen species generation, promoted early apoptosis, and resulted in DNA damage in mouse oocytes. Moreover, DEHP exposure caused mitochondrial damage, reduced ATP content, down-regulated actin expression, and disturbed the spindle assembly and chromosome alignment in mouse oocytes. Furthermore, DEHP exposure remarkably impaired the localization and protein level of Juno, the sperm receptor on the membrane of oocytes. The levels of DNA methylation, H3K9me3, and H3K9ac were also altered in the DEHP-exposed mouse oocytes. Thus, our results indicated that DEHP exposure reduced the maturation and fertilization capabilities of mouse oocytes by affecting cytoskeletal dynamics, oxidative stress, early apoptosis, meiotic spindle morphology, mitochondria, ATP content, Juno expression, DNA damage, and epigenetic modifications in mouse oocytes.

摘要

邻苯二甲酸二(2-乙基己基)酯(DEHP)是聚氯乙烯(PVC)塑料中广泛使用的增塑剂。人类和动物广泛且持续地接触 DEHP,尤其是饮食方面,这与生殖疾病有关。然而,DEHP 暴露对体内卵母细胞的影响和潜在机制仍不清楚。在本研究中,我们发现,DEHP 的口服给药(每天 40μg/kg 体重,持续 14 天)显著降低了体内卵母细胞的成熟和受精能力。此外,DEHP 引起氧化应激,增加活性氧的产生,促进早期细胞凋亡,并导致小鼠卵母细胞的 DNA 损伤。此外,DEHP 暴露导致线粒体损伤,降低 ATP 含量,下调肌动蛋白表达,并扰乱小鼠卵母细胞的纺锤体组装和染色体排列。此外,DEHP 暴露显著损害了 Juno 的定位和蛋白水平,Juno 是卵母细胞膜上的精子受体。暴露于 DEHP 的小鼠卵母细胞中的 DNA 甲基化、H3K9me3 和 H3K9ac 水平也发生了改变。因此,我们的结果表明,DEHP 暴露通过影响细胞骨架动力学、氧化应激、早期细胞凋亡、减数分裂纺锤体形态、线粒体、ATP 含量、Juno 表达、DNA 损伤和表观遗传修饰来降低小鼠卵母细胞的成熟和受精能力。

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