Van Blerkom J, Davis P
Colorado Reproductive Endocrinology, Rose Medical Center, Denver, CO 80220, USA.
Hum Reprod. 2001 Apr;16(4):757-64. doi: 10.1093/humrep/16.4.757.
The effects of four rounds of ovarian stimulation spaced 1-6 weeks apart on the normality of metaphase II (MII) spindle formation, chromosomal alignment and cytoplasmic organization were examined in intact ovulated mouse oocytes and at MII for oocytes obtained at the germinal vesicle stage from the same ovaries and matured in vitro. The terminal deoxynucleotidyl transferase-mediated dUDP nick-end labelling assay was used to identify DNA strand breaks in chromosomes, and histological studies of ovaries between and at each round of ovarian stimulation were performed. The results demonstrate a progressive and significant increase in the frequency of spindle defects with each round of ovarian stimulation, including those spaced weeks apart. Oocytes with spindle defects were also characterized by the occurrence of detached chromosomes and cytoplasmic asters. In contrast, in-vitro matured oocytes derived from the same ovaries were normal. No evidence of DNA strand breaks with repeated rounds of ovarian stimulation was detected in ovulated or in-vitro matured oocytes. The development and persistence of nodules of hypertrophied granulosa in regions where follicular growth occurs suggest that a progressively increasing proportion of oocytes in the ovulatory pathway may experience an intrafollicular milieu that has negative consequences for competence. The results are discussed with respect to ovarian and oocyte biological ageing and possible adverse implications for human oocyte competence with repeated hyperstimulation.
研究了间隔1 - 6周进行的四轮卵巢刺激对完整排卵小鼠卵母细胞以及从同一卵巢的生发泡期获取并在体外成熟至中期II(MII)的卵母细胞的MII纺锤体形成、染色体排列和细胞质组织正常性的影响。采用末端脱氧核苷酸转移酶介导的dUDP缺口末端标记试验来识别染色体中的DNA链断裂,并对每轮卵巢刺激之间及刺激时的卵巢进行组织学研究。结果表明,每轮卵巢刺激,包括间隔数周的刺激,纺锤体缺陷的频率都有渐进性显著增加。有纺锤体缺陷的卵母细胞还表现为染色体分离和细胞质星体的出现。相比之下,来自同一卵巢的体外成熟卵母细胞是正常的。在排卵或体外成熟的卵母细胞中,未检测到重复进行卵巢刺激导致DNA链断裂的证据。卵泡生长区域肥大颗粒细胞结节的发展和持续存在表明,排卵途径中卵母细胞经历卵泡内环境对其能力产生负面影响的比例可能逐渐增加。针对卵巢和卵母细胞的生物学衰老以及反复超刺激对人类卵母细胞能力可能产生的不利影响对结果进行了讨论。