首页> 外文期刊>Animal Reproduction Science >Development of in vitro embryo production systems for red deer (Cervus elaphus) Part 3. In vitro fertilisation using sheep serum as a capacitating agent and the subsequent birth of calves
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Development of in vitro embryo production systems for red deer (Cervus elaphus) Part 3. In vitro fertilisation using sheep serum as a capacitating agent and the subsequent birth of calves

机译:马鹿体外胚胎生产系统的开发第3部分。以绵羊血清为诱捕剂并随后出生小牛的体外受精

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The following experiments investigated the use of sheep serum (SS) as a capacitating agent for red deer (Cervus elaphus) sperm during in vitro fertilisation. Red deer oocytes were collected at slaughter and matured in vitro for 24h in TCM-199 supplemented with 10% foetal calf serum, 10 mug ml(-1) FSH and LH, and 1 mug ml(-1) of oestradiol. Fertilisation medium was IVF-SOF modified to contain 5 mM Ca2+ and no glucose. Experiment 1 investigated the addition of heparin, BSA (8 mg ml(-1)) or 20% SS. All oocytes were penetrated when IVF-SOF was supplemented with SS compared to 10 and 0% penetration when either heparin or BSA was present (P < 0.01). However, 43.8% of these oocytes were polyspermic when the medium contained SS. In Experiment 2, the effect of sperm concentration on penetration rates during in vitro fertilisation was investigated. Total sperm penetration and monospermic penetration rates increased with increased sperm concentrations in a log linear manner (P < 0.001) and both approached an asymptote at 0.4 x 10(6) sperm ml(-1) with 93.6 and 77% for total and monospermic penetration, respectively. Polyspermic fertilisation also increased with increasing sperm concentrations (P < 0.05) but was variable (range 3.5+/-4.2 to 42.3+/-10.6%), especially at the lower sperm concentrations. Experiment 3 investigated the viability of these oocytes after transfer into red deer recipients. Fifteen 2- and 4-cell embryos were transferred into the oviducts of synchronized recipients 28 h post in vitro insemination. An additional fourteen embryos (8-10 cell) were transferred into synchronised recipients after 48 h of in vitro culture in either SOFaaBSA (n = 10) or on red deer epithelial oviduct monolayers (n = 4).Five (33% 5/15) of the recipients that received 2- and 4-cell embryos were pregnant at Day 45 (verified by ultrasonography) and four recipients subsequently calved. One recipient receiving an embryo cultured in SOFaaBSA was pregnant at Day 45 and subsequently calved. The birth of five normal calves indicate that full developmental competence of red deer oocytes matured and fertilised in vitro can be achieved by the techniques described.
机译:以下实验研究了在体外受精过程中使用绵羊血清(SS)作为马鹿精子的致电容剂。屠宰时收集马鹿卵母细胞,并在补充有10%胎牛血清,10杯ml(-1)FSH和LH和1杯ml(-1)雌二醇的TCM-199中体外成熟24小时。施肥培养基经过IVF-SOF修饰,含有5 mM Ca2 +,不含葡萄糖。实验1研究了肝素,BSA(8 mg ml(-1))或20%SS的添加。 IVF-SOF补充SS后,所有卵母细胞均被穿透,而肝素或BSA则分别穿透10%和0%(P <0.01)。但是,当培养基中含有SS时,这些卵母细胞中有43.8%是多精子的。在实验2中,研究了精子浓度对体外受精过程中渗透率的影响。随着精子浓度的增加,总精子穿透率和单精子穿透率以对数线性方式增加(P <0.001),并且两者均以0.4 x 10(6)精子ml(-1)接近渐近线,总和单精子穿透率为93.6和77% , 分别。多精子受精也随着精子浓度的增加而增加(P <0.05),但变化不定(范围为3.5 +/- 4.2至42.3 +/- 10.6%),尤其是在较低的精子浓度下。实验3研究了这些卵母细胞转移到马鹿受体后的生存力。体外受精后28小时,将15个2细胞和4细胞胚胎转移到同步受体的输卵管中。在SOFaaBSA(n = 10)或马鹿上皮输卵管单层(n = 4)上进行体外培养48 h后,将另外的14个胚胎(8-10个细胞)转移到同步受体中。五个(33%5/15)接受了2细胞和4细胞胚胎的接受者在第45天怀孕(通过超声检查),随后有4位接受者产犊。一位接受SOFaaBSA培养的胚胎的受者在第45天怀孕,随后分娩。五只正常牛的出生表明,通过所述技术可以实现体外成熟和受精的马鹿卵母细胞的全部发育能力。

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