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Holding equine oocytes in a commercial embryo-holding medium: New perspective on holding temperature and maturation time

机译:将马卵母细胞保存在商业胚胎保存培养基中:保存温度和成熟时间的新观点

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In the present study, we examined the effect of holding equine oocytes in Syngro embryo holding medium (EHM) overnight at either 4 degrees C, 17 degrees C, or 22 degrees C to 25 degrees C, on the time to maturation and developmental competence. We also examined the effect of placing denuded oocyte without extruded polar body back in maturation condition on subsequent maturation rate. In experiment 1, cumulus-oocyte complexes (COCs) were recovered postmortem and placed in EHM at 22 degrees C to 25 degrees C for 18 to 20 hours (OH) or placed directly in maturation (DM). The maturation rate was assessed after 22, 24, or 28 hours of culture. After denuding cumulus cells at 22 or 24 hours, oocytes without obvious polar body were placed back into culture and reassessed at subsequent time points. At 22 hours, a higher proportion of oocytes placed in OH achieved nuclear maturation than those placed in DM (63% and 37%, respectively, P = 0.008). At 24 and 28 hours, no significant differences in the % NO stage oocytes were observed between OH and DM. The nuclear maturation rate for OH oocytes was similar at 22, 24, and 28 hours, indicating that the maximum maturation rate was reached at an earlier time than that in DM. Oocytes fertilized by intracytoplasmic sperm injection resulted in a 7.1% and 6.3% blastocyst rate for OH and DM, respectively. Denuding oocytes after 22 hours or more of culture did not have an adverse effect on the final nuclear maturation rate. After 28 hours of culture, the same nuclear maturation rate (MII) was reached for nondenuded oocytes and oocytes denuded after 22 hours of 24 hours of culture. In experiment 2, COCs were held overnight at room temperature in EHM, then placed in maturation for 20, 22, and 28 hours. Nuclear maturation rate was significantly lower at 20 hours than 22 and 28 hours of culture and was similar at 22 and 28 hours, suggesting that at least 22 hours of culture is required to reach maximal maturation rate for stored oocytes (43%, 62%, and 65% at 20, 22, and 28 hours, respectively. P 0.001). In experiment 3, COCs were either placed directly in culture or held at 22 degrees C to 25 degrees C, 17 degrees C, or 4 degrees C overnight. After 24 hours of culture, maturation rate was similar for all groups, suggesting that COCs can be stored in conventional 4 degrees C transport condition or 17 degrees C. In preliminary studies, COCs were held at 4 degrees C followed by 24 hours of culture, and mature oocytes were fertilized using intracytoplasmic sperm injection. Twenty-three injected oocytes yielded four blastocysts. In conclusion, we reported that oocytes can be placed in a commercial EHM and stored overnight without a detrimental effect on maturation rates or blastocyst development. Oocytes held in holding medium require less time to reach the MII stage than oocytes placed in culture directly. Removing the cumulus cells from oocytes that have been cultured for at least 22 hours does not seem to alter the final nuclear maturation rate. Finally, we observed no detrimental effect of storing oocytes at 4 degrees C for up to 18 hours, and oocytes appeared to maintain developmental competence and blastocyst potential. (C) 2016 Elsevier Inc. All rights reserved.
机译:在本研究中,我们研究了在4摄氏度,17摄氏度或22摄氏度至25摄氏度的条件下,将马卵母细胞在Syngro胚胎保持培养基(EHM)中保持过夜对成熟时间和发育能力的影响。我们还研究了将裸露的卵母细胞在未成熟的情况下放回成熟状态对随后的成熟速率的影响。在实验1中,在验尸后回收卵母细胞复合物(COC),并在22到25摄氏度的EHM中放置18到20个小时(OH),或直接放置在成熟状态(DM)中。培养22、24或28小时后评估成熟率。在22或24小时剥落卵丘细胞后,将没有明显极体的卵母细胞放回培养物中,并在随后的时间点重新评估。在22小时时,放置在OH中的卵母细胞比例高于放置在DM中的卵母细胞(分别为63%和37%,P = 0.008)。在24小时和28小时,在OH和DM之间没有观察到NO期卵母细胞%的显着差异。 OH卵母细胞在22、24和28小时的核成熟率相似,这表明最大成熟率要比DM早。通过胞浆内精子注射受精的卵母细胞的OH和DM囊胚率分别为7.1%和6.3%。培养22小时或更长时间后剥去卵母细胞对最终核成熟率没有不利影响。培养28小时后,未裸露的卵母细胞和培养24小时的22小时后裸露的卵母细胞达到相同的核成熟率(MII)。在实验2中,将COC在EHM中于室温下放置过夜,然后放置20、22和28小时进行熟化。在20小时时的核成熟率显着低于22和28小时的培养,并且在22和28小时时相似,这表明至少需要22小时的培养才能达到卵母细胞的最大成熟率(43%,62%,和分别在20、22和28小时时达到65%(P <0.001)。在实验3中,将COC直接放置在培养物中或在22摄氏度至25摄氏度,17摄氏度或4摄氏度的温度下放置过夜。培养24小时后,所有组的成熟率均相似,这表明COC可以在常规的4摄氏度运输条件或17摄氏度下储存。在初步研究中,将COC保持在4摄氏度,然后进行24个小时的培养,成熟卵母细胞通过胞浆内精子注射进行受精。注射的二十三个卵母细胞产生了四个囊胚。总之,我们报道了卵母细胞可以放置在商业EHM中并过夜保存,而对成熟速率或胚泡发育没有不利影响。与直接置于培养物中的卵母细胞相比,保持在卵母细胞中的卵母细胞达到MII阶段所需的时间更少。从已经培养了至少22小时的卵母细胞中去除卵丘细胞似乎不会改变最终的核成熟率。最后,我们没有观察到将卵母细胞在4摄氏度下储存长达18小时的有害影响,并且卵母细胞似乎可以保持发育能力和囊胚潜能。 (C)2016 Elsevier Inc.保留所有权利。

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