In vivo and in vitro postovulatory aging: when time works against oocyte quality?

被引:44
作者
Di Nisio, Valentina [1 ,2 ]
Antonouli, Sevastiani [3 ]
Damdimopoulou, Pauliina [1 ,2 ]
Salumets, Andres [1 ,2 ,4 ,5 ]
Cecconi, Sandra [3 ]
机构
[1] Karolinska Inst, Dept Clin Sci Intervent & Technol, Div Obstet & Gynecol, S-14186 Stockholm, Sweden
[2] Karolinska Univ Hosp, S-14186 Stockholm, Sweden
[3] Univ Aquila, Dept Life Hlth & Environm Sci, Via Vetoio, I-67100 Laquila, Italy
[4] Univ Tartu, Inst Clin Med, Dept Obstet & Gynaecol, EE-50406 Tartu, Estonia
[5] Competence Ctr Hlth Technol, EE-50411 Tartu, Estonia
关键词
Postovulatory aging; Oocyte; Oxidative stress; Morphological alteration; Assisted reproductive technology; Antiaging chemicals; AGED MOUSE OOCYTES; CORTICAL GRANULE EXOCYTOSIS; POOR EMBRYO DEVELOPMENT; OXIDATIVE STRESS; SPONTANEOUS ACTIVATION; PORCINE OOCYTES; REDOX STATUS; EXPRESSION; SPINDLE; ABNORMALITIES;
D O I
10.1007/s10815-022-02418-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In mammalian species an optimal fertilization window during which successful fertilization occurs. In the majority of mammals estrus marks ovulation time and coincident with mating, thereby allowing the synchronized meeting in the fallopian tubes, between freshly ejaculated sperm and freshly ovulated oocytes. Conversely, women do not show natural visual signs of ovulation such that fertilization can occur hours later involving an aged oocyte and freshly ejaculated spermatozoa. During this time, the oocyte undergoes a rapid degradation known as "postovulatory aging" (POA). POA may become particularly important in the human-assisted reproductive technologies, as the fertilization of retrieved mature oocytes can be delayed due to increased laboratory workload or because of unforeseeable circumstances, like the delayed availability of semen samples. This paper is an updated review of the consequences of POA, either in vivo or in vitro, on oocyte quality with particular attention to modifications caused by POA on oocyte nuclear, cytoplasmic, genomic, and epigenetic maturation, and embryo development.
引用
收藏
页码:905 / 918
页数:14
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