Cao Lian Bao, Liu Hong Bin, Lu Gang, Lv Yue, Leung Chi Kwan, Du Yan Zhi, Wang Wu Ming, Xiong Zhi Qiang, Su Xian Wei, Li Hong Jian, Chen Zi-Jiang, Ma Jin Long, Chan Wai Yee
Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan, China.
CUHK-SDU Joint Laboratory on Reproductive Genetics, School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Front Cell Dev Biol. 2020 Jul 31;8:587. doi: 10.3389/fcell.2020.00587. eCollection 2020.
4-vinylcyclohexene diepoxide (VCD) has long been considered a hazardous occupational chemical that promotes ovarian failure. However, VCD is also used as a research compound to chemically induce animal models of premature ovarian insufficiency (POI), and in related work we unexpectedly found that VCD apparently exhibits both dose- and duration-dependent opposing, hormone-like effects on the maintenance of the primordial follicle pool, follicle development, and ovulation induction.
We conducted experiments with cultured murine ovaries and performed transplantation experiments using postnatal day (PD) 2 and PD12 mice and found that low-dose, short-term exposure to VCD (VCD) actually protects the primordial/primary follicle pool and improves the functional ovarian reserve (FOR) by disrupting follicular atresia. VCD inhibits follicular apoptosis and regulates the Pten-PI3K-Foxo3a pathway. Short-term VCD exposure (80 mg/kg, 5 days) significantly increases the number of superovulated metaphase II oocytes, preovulatory follicles, and corpus luteum in middle-aged mice with diminished ovarian reserve (DOR). We demonstrate that low-dose but not high-dose VCD promotes aromatase levels in granulosa cells (GCs), thereby enhancing the levels of estradiol secretion.
Our study illustrates a previously unappreciated, hormone-like action for the occupational "ovotoxin" molecule VCD and strongly suggests that VCD should be explored for its potential utility for treating human ovarian follicular development disorders, including subfertility in perimenopausal women.
4-乙烯基环己烯二环氧化物(VCD)长期以来被认为是一种会导致卵巢功能衰竭的有害职业化学品。然而,VCD也被用作一种研究化合物,用于化学诱导卵巢早衰(POI)的动物模型,在相关研究中我们意外发现,VCD对原始卵泡池的维持、卵泡发育和排卵诱导显然呈现出剂量和持续时间依赖性的相反的、类似激素的作用。
我们用培养的小鼠卵巢进行了实验,并使用出生后第2天(PD2)和第12天(PD12)的小鼠进行了移植实验,发现低剂量、短期暴露于VCD实际上通过破坏卵泡闭锁来保护原始/初级卵泡池并改善功能性卵巢储备(FOR)。VCD抑制卵泡凋亡并调节Pten-PI3K-Foxo3a信号通路。短期VCD暴露(80mg/kg,5天)显著增加了卵巢储备功能减退(DOR)的中年小鼠超排卵中期II期卵母细胞、排卵前卵泡和黄体的数量。我们证明低剂量而非高剂量的VCD可促进颗粒细胞(GCs)中芳香化酶水平,从而提高雌二醇分泌水平。
我们的研究揭示了职业性“卵巢毒素”分子VCD一种此前未被认识的类似激素的作用,并强烈表明应探索VCD在治疗人类卵巢卵泡发育障碍(包括围绝经期妇女的生育力低下)方面的潜在效用。