Maternal age and gonadotrophin elevation cooperatively decrease viable ovulated oocytes and increase ootoxicity, chromosome-, and spindle-misalignments: '2-Hit' and 'FSH-OoToxicity' mechanisms as new reproductive aging hypotheses.

IF 3.6 2区 医学 Q2 DEVELOPMENTAL BIOLOGY Molecular human reproduction Pub Date : 2023-09-30 DOI:10.1093/molehr/gaad030
Lori R Bernstein, Amelia C L Mackenzie, Keith Durkin, Duane C Kraemer, Charles L Chaffin, Istvan Merchenthaler
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Abstract

While there is consensus that advanced maternal age (AMA) reduces oocyte yield and quality, the notion that high FSH reduces oocyte quality and causes aneuploidy remains controversial, perhaps due to difficulties controlling the confounding variables of age and FSH levels. Here, contributions of age and gonadotrophin elevation were separately controlled using a mouse model of human female reproductive aging. Ovulated oocytes were collected from young and midlife mice after 0-, 2.6-, or 17-day treatment with the FSH analog equine chorionic gonadotrophin (eCG), to model both exogenous FSH elevation within a single treatment cycle (as in controlled ovarian stimulation (COS)), and chronic endogenous FSH elevation during multiple cycles (as in diminished ovarian reserve). After 17-day eCG, fewer total oocytes/mouse are ovulated in midlife than young mice, and a precipitous decline in viable oocytes/mouse is observed in midlife but not young mice throughout eCG treatment. eCG is potently ootoxic to ovulatory oocytes and strongly induces chromosome- and spindle-misalignments within 2.6 days of eCG in midlife, but only after 17 days in young mice. These data indicate that AMA increases susceptibility to multiple adverse effects of elevated FSH activity in ovulated oocytes, including declines in total and viable oocytes/mouse, and induction of ootoxicity and aneuploidy. Two hypotheses are proposed for underlying causes of infertility in women. The FSH OOToxicity Hypothesis ('FOOT Hypothesis') posits that high FSH is ootoxic to ovulatory oocytes and that FSH ootoxicity is a root cause of low pregnancy success rates in naturally cycling women with high FSH and IUI patients undergoing COS. The '2-Hit Hypothesis' posits that AMA increases susceptibility to FSH-induced ootoxicity and aneuploidy.

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母体年龄和促性腺激素升高共同降低了可存活的排卵卵母细胞,增加了卵毒性、染色体和纺锤体错位:“2-命中”和“FSH-卵毒性”机制是新的生殖衰老假说。
虽然人们一致认为高龄产妇会降低卵母细胞产量和质量,但高FSH会降低卵细胞质量并导致非整倍体的观点仍然存在争议,可能是因为难以控制年龄和FSH水平的混杂变量。在这里,使用人类女性生殖衰老的小鼠模型分别控制年龄和促性腺激素升高的贡献。在用FSH类似物马绒毛膜促性腺激素(eCG)治疗0、2.6或17天后,从年轻和中年小鼠中收集卵母细胞,以模拟单个治疗周期内外源性FSH升高(如控制性卵巢刺激(COS))和多个周期内慢性内源性FSH升高的模型(如卵巢储备减少)。在17天的eCG后,中年时排卵的总卵母细胞/小鼠比年轻小鼠少,并且在整个eCG治疗过程中,观察到中年但年轻小鼠的活卵母细胞数急剧下降。eCG对排卵卵母细胞具有强大的卵毒性,并在2.6范围内强烈诱导染色体和纺锤体错位 中年时的eCG天数,但仅在17天后 幼鼠的天数。这些数据表明,AMA增加了排卵卵母细胞中FSH活性升高的多种不良反应的易感性,包括总卵母细胞和活卵母细胞/小鼠的减少,以及卵毒性和非整倍体的诱导。针对女性不孕的根本原因,提出了两种假说。FSH卵毒性假说(“FOOT假说”)认为,高FSH对排卵卵母细胞具有卵毒性,而FSH卵毒是接受COS的具有高FSH和IUI患者的自然循环女性妊娠成功率低的根本原因。“2-Hit假说”认为AMA增加了对FSH诱导的卵毒性和非整倍体的易感性。
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来源期刊
Molecular human reproduction
Molecular human reproduction 生物-发育生物学
CiteScore
8.30
自引率
0.00%
发文量
37
审稿时长
6-12 weeks
期刊介绍: MHR publishes original research reports, commentaries and reviews on topics in the basic science of reproduction, including: reproductive tract physiology and pathology; gonad function and gametogenesis; fertilization; embryo development; implantation; and pregnancy and parturition. Irrespective of the study subject, research papers should have a mechanistic aspect.
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