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长期冷藏后体外成熟和受精的家猫卵母细胞发育成囊胚。

Development to blastocysts of domestic cat oocytes matured and fertilized in vitro after prolonged cold storage.

作者信息

Wolfe B A, Wildt D E

机构信息

National Zoological Park, Conservation and Research Center, Smithsonian Institution, Front Royal, VA 22630, USA.

出版信息

J Reprod Fertil. 1996 Jan;106(1):135-41. doi: 10.1530/jrf.0.1060135.

Abstract

Four experiments determined the kinetics of in vitro maturation and fertilization of cat oocytes and the effects of prolonged cold storage of ovaries before oocyte recovery on in vitro maturation/in vitro fertilization (IVM/IVF) success. Domestic cat ovaries were collected at ovariohysterectomy and stored at 4 degrees C in PBS until oocyte recovery and culture in Eagle's minimal essential medium (EMEM) containing FSH, LH, oestradiol and BSA for maturation. In Expt 1, meiotic maturation was assessed at 0, 12, 24, 38 and 48 h of culture. After 24 h, > 61% of oocytes were in telophase I or metaphase II. In Expt 2, oocytes were recovered from ovaries stored for 24, 48 or 72 h and cultured in EMEM for 24 h. There was no difference among groups (P > 0.05) in the ability to achieve nuclear maturation (mean +/- SEM, 57.1 +/- 5.3%, 60.4 +/- 5.4%, 55.4 +/- 15.1% for 24, 48 and 72 h, respectively). Fertilization and embryo development after insemination at 16, 24, 32, 40 and 48 h of culture were examined in Expt 3. Of 98 oocytes inseminated at 32 h, 69% cleaved, 59% developed into morulae and 13% into blastocysts, more (P < 0.05) than those oocytes inseminated at earlier and later times. Development to blastocysts occurred after insemination at 16 (1.2%), 24 (9.1%) and 32 (13.3%) h of culture, but not after insemination at 40 or 48 h. Expt 4 involved cold storage of ovaries for 24, 48 or 72 h before oocyte recovery and insemination at 32 h of culture (the optimal time measured in Expt 3). Compared with storage for 24 h, fertilization success was lower (P < 0.05) in the 48 and 72 h groups, and, although 9.1% of inseminated oocytes from the 24 h storage group developed to blastocysts, none (P < 0.05) achieved this stage after 48 or 72 h of storage. These results indicate that domestic cat oocytes reach nuclear maturity by 24 h in culture and can be fertilized and develop to blastocysts optimally after insemination at 32 h. Oocytes recovered from ovaries stored at 4 degrees C for up to 72 h are capable of reaching telophase I or metaphase II in vitro. However, only oocytes stored within the ovary for 24 h produce blastocysts, indicating that the ability to achieve nuclear maturation is an inadequate indicator of fertilization and developmental competence.

摘要

四项实验确定了猫卵母细胞的体外成熟和受精动力学,以及在卵母细胞回收前卵巢长时间冷藏对体外成熟/体外受精(IVM/IVF)成功率的影响。在卵巢子宫切除术中收集家猫卵巢,保存在4℃的PBS中,直至回收卵母细胞,并在含有促卵泡素(FSH)、促黄体素(LH)、雌二醇和牛血清白蛋白(BSA)的伊格尔氏基础培养基(EMEM)中培养以使其成熟。在实验1中,在培养0、12、24、38和48小时时评估减数分裂成熟情况。24小时后,超过61%的卵母细胞处于第一次减数分裂末期或第二次减数分裂中期。在实验2中,从储存24、48或72小时的卵巢中回收卵母细胞,并在EMEM中培养24小时。各组在实现核成熟的能力方面无差异(P>0.05)(分别在24、48和72小时时,平均±标准误为57.1±5.3%、60.4±5.4%、55.4±15.1%)。在实验3中,检查培养16、24、32、40和48小时后授精的受精和胚胎发育情况。在培养32小时授精的98个卵母细胞中,69%发生分裂,59%发育成桑椹胚,13%发育成囊胚,比在更早和更晚时间授精的卵母细胞更多(P<0.05)。在培养16(1.2%)、24(9.1%)和32(13.3%)小时后授精可发育成囊胚,但在40或48小时后授精则不能。实验4包括在卵母细胞回收前将卵巢冷藏24、48或72小时,并在培养32小时(实验3中测得的最佳时间)时授精。与储存24小时相比,48和72小时组的受精成功率较低(P<0.05),并且,虽然储存24小时组9.1%的授精卵母细胞发育成囊胚,但储存48或72小时后无一发育至此阶段(P<0.05)。这些结果表明,家猫卵母细胞在培养24小时时达到核成熟,在32小时授精后能够最佳地受精并发育成囊胚。从4℃储存长达72小时的卵巢中回收的卵母细胞能够在体外达到第一次减数分裂末期或第二次减数分裂中期。然而,只有在卵巢内储存24小时的卵母细胞才能产生囊胚,这表明实现核成熟的能力并不能充分指示受精和发育能力。

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