| Literature DB >> 27956222 |
Zhiguo Zhang1, Tianjuan Wang2, Yan Hao2, Fazil Panhwar3, Zhongrong Chen3, Weiwei Zou2, Dongmei Ji2, Beili Chen2, Ping Zhou2, Gang Zhao4, Yunxia Cao5.
Abstract
Sucrose and trehalose are conventional cryoprotectant additives for oocytes and embryos. Ethanol can artificially enhance activation of inseminated mature oocytes. This study aims to investigate whether artificial oocyte activation (AOA) with ethanol can promote the development competence of in vitro matured oocytes. A total of 810 human immature oocytes, obtained from 325 patients undergoing normal stimulated oocyte retrieval cycles, were in vitro maturated (IVM) either immediately after collection (Fresh group n = 291)) or after being vitrified as immature oocytes (Vitrified group n = 519). These groups were arbitrarily assigned. All fresh and vitrified oocytes which matured after a period of IVM then underwent intra-cytoplasmic sperm injection (ICSI). Half an hour following ICSI, they were either activated by 7% ethanol (AOA group) or left untreated (Non-AOA group). Fertilization, cleavage rate, blastocyst quality and aneuploidy rate were then evaluated. High-quality blastocysts were only obtained in both the fresh and vitrified groups which had undergone AOA after ICSI. Trehalose vitrification slightly, but not significantly, increased the formation rates of high-quality embryos (21.7% VS 15.4%, P > 0.05) and blastocysts (15.7% VS 7.69%, P > 0.05)) when compared with sucrose vitrification. Aneuploidy was observed in 12 of 24 (50%) of the AOA derived high quality blastocysts. High-quality blastocysts only developed from fresh or vitrified immature oocytes if the ICSI was followed by AOA. This information may be important for human immature oocytes commonly retrieved in normal stimulation cycles and may be particularly important for certain patient groups, such as cancer patients. AOA with an appropriate concentration of ethanol can enhance the developmental competence of embryos.Entities:
Keywords: Aneuploidy; Artificial oocyte activation (AOA); Fluorescence in situ hybridization (FISH); Human immature oocytes; Trehalose vitrification
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Year: 2016 PMID: 27956222 DOI: 10.1016/j.cryobiol.2016.12.004
Source DB: PubMed Journal: Cryobiology ISSN: 0011-2240 Impact factor: 2.487