Adverse effects of 2-Methoxyestradiol on mouse oocytes during reproductive aging

2-Methoxyestradiol (2-ME2) is a metabolite of 17β-estradiol and is currently in clinical trials as an antitumor agent. Here we found 2-ME2 level remains stable in the local environment of ovaries but declines in serum in aging mice, and exogenous 2-ME2 impacts the meiotic maturation of mouse oocytes...

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Veröffentlicht in:Chemico-biological interactions 2023-01, Vol.369, p.110277-110277, Article 110277
Hauptverfasser: Jiang, Xiuying, Xu, Xiangning, Wang, Bicheng, Song, Ke, Zhang, Jiaqi, Chen, Ye, Tian, Ying, Weng, Jing, Liang, Yuanjing, Ma, Wei
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Sprache:eng
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Zusammenfassung:2-Methoxyestradiol (2-ME2) is a metabolite of 17β-estradiol and is currently in clinical trials as an antitumor agent. Here we found 2-ME2 level remains stable in the local environment of ovaries but declines in serum in aging mice, and exogenous 2-ME2 impacts the meiotic maturation of mouse oocytes in dose-dependent manner. In vitro 2-ME2 application arrested oocytes at metaphase I (MI), with abnormal spindle structure and chromosome alignment. 2-ME2 exposure induced excessive production of reactive oxygen species (ROS) and malondialdehyde, as well as accelerated apoptosis progression. 2-ME2 unbalanced mitochondrial dynamics by increasing DRP1 and MFN1 while decreasing Opa1. Similar phenotypes were also observed in oocytes from mice injected intraperitoneally with 2-ME2. Taken together, this study indicates 2-ME2 exposure impairs oocyte meiotic maturation through inducing mitochondrial imbalance, oxidative stress and apoptosis. The gradual decline in oocyte quality and quantity may be associated with the stable 2-ME2 in ovaries during female reproductive aging. [Display omitted] •2-ME2 level remains stable in ovarian while declines in serum in aging mice.•2-ME2 dose-dependently induces mitochondria dysfunction, oxidative stress and apoptotic progression in oocytes.•2-ME2 exposure impacts spindle, chromosome alignment and meiotic maturation in oocytes.
ISSN:0009-2797
1872-7786
DOI:10.1016/j.cbi.2022.110277