Izquierdo D, Villamediana P, Palomo M J, Mogas T, Paramio M T
Departament de Patologia i de Producció Animal, Universitat Autònoma de Barcelona, Bellaterra, Spain.
Theriogenology. 1998 Jun;49(8):1501-13. doi: 10.1016/s0093-691x(98)00096-x.
Experiments were carried out to develop an improved IVF system for prepubertal goat oocytes matured in vitro. Cumulus oocyte complexes (COC) were obtained by slicing ovaries from slaughtered prepubertal goats. Oocytes were matured in TCM199 supplemented with 20% estrous goat serum (EGS) + 10 micrograms/mL FSH + 10 micrograms/mL LH + 1 microgram/mL estradiol 17 beta for 27 h at 38.5 degrees C in 5% CO2 in air. In Experiments 1 and 2, freshly ejaculated spermatozoa were capacitated in 1 of 3 media: TALP/H, modified Defined Medium (mDM) and mH-M199 with 50 micrograms/mL heparin for 45 min. Matured oocytes were fertilized in TALP, mDM or mH-M199 in Experiment 1 and in TALP in Experiment 2. In Experiment 3, three media were used for sperm capacitation and fertilization: Treatment A (control group): spermatozoa were capacitated in mDM with 50 micrograms/mL heparin for 45 min and fertilized in TALP medium with 1 microgram/mL hypotaurine; Treatment B: spermatozoa were capacitated in mDM with 50 micrograms/mL heparin + 388 micrograms/mL caffeine for 30 min and fertilized in TALP medium without hypotaurine; Treatment C: spermatozoa were capacitated in mDM with 50 micrograms/mL heparin for 45 min and fertilized in TALP medium with PHE (20 microM penicillamine, 10 microM hypotaurine and 2 microM epinephrine). At 24 h post insemination, the ova were transferred to a granulosa cell monolayer, and early embryo development was evaluated until Day 8. In experiment 2, the results show, that mDM plus heparin for sperm capacitation and TALP medium with hypotaurine for oocyte fertilization provided the highest proportion of penetrated oocytes, both total number (79.6%) and normal fertilization (55.1%), whereas the use of caffeine (44.6 and 31.2%, total and normal fertilization rate, respectively) and PHE (31.8 and 20.6%, total and normal fertilization rate, respectively) as motility enhancers did not improve the results obtained in the control group (48.7% and 37.2%, total and normal fertilization rate, respectively). These were no differences for the results of morulae and blastocysts.
开展了实验以开发一种改进的体外受精(IVF)系统,用于体外成熟的青春期前山羊卵母细胞。通过切割屠宰的青春期前山羊的卵巢获得卵丘卵母细胞复合体(COC)。卵母细胞在补充有20%发情山羊血清(EGS)+10微克/毫升促卵泡素(FSH)+10微克/毫升促黄体生成素(LH)+1微克/毫升17β-雌二醇的TCM199中,于38.5℃、5%二氧化碳的空气中培养27小时使其成熟。在实验1和实验2中,将新鲜射出的精子在3种培养基中的1种中进行获能处理:输卵管液/重碳酸盐缓冲液(TALP/H)、改良限定培养基(mDM)和添加50微克/毫升肝素的改良哈姆氏F10培养基(mH-M199),处理45分钟。在实验1中,成熟的卵母细胞在TALP、mDM或mH-M199中进行受精,在实验2中则在TALP中受精。在实验3中,使用3种培养基进行精子获能和受精:处理A(对照组):精子在添加50微克/毫升肝素的mDM中获能45分钟,并在添加1微克/毫升亚牛磺酸的TALP培养基中受精;处理B:精子在添加50微克/毫升肝素+388微克/毫升咖啡因的mDM中获能30分钟,并在不添加亚牛磺酸的TALP培养基中受精;处理C:精子在添加50微克/毫升肝素的mDM中获能45分钟,并在添加苯丙氨酸(20微摩尔青霉胺、10微摩尔亚牛磺酸和2微摩尔肾上腺素)的TALP培养基中受精。授精后24小时,将卵子转移至颗粒细胞单层,并评估早期胚胎发育直至第8天。在实验2中,结果显示,使用mDM加肝素进行精子获能以及使用添加亚牛磺酸的TALP培养基进行卵母细胞受精时,穿透卵母细胞的比例最高,无论是总数(79.6%)还是正常受精率(55.1%),而使用咖啡因(总数和正常受精率分别为44.6%和31.2%)和苯丙氨酸(总数和正常受精率分别为31.8%和20.6%)作为活力增强剂并未改善对照组所获得的结果(总数和正常受精率分别为48.7%和37.2%)。桑椹胚和囊胚的结果没有差异。