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Effect of angiotensin II with follicle cells and insulin-like growth factor-I or insulin on bovine oocyte maturation and embryo development

机译:血管紧张素II与卵泡细胞和胰岛素样生长因子-I或胰岛素对牛卵母细胞成熟和胚胎发育的影响

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The objective was to evaluate the effects of angiotensin II (Ang II), insulin-like growth factor-I (IGF-I) and insulin on the nuclear and cytoplasmic maturation of bovine oocytes in the presence of follicular cells. Cumulus-oocyte complexes (COCs) were cultured for 22h in the presence of follicular cells (control with cells) and Ang II, IGF-I or insulin (treatments), or in the absence of follicular cells (control without cells). Using these five groups, Experiment 1 was conducted with and without the addition of gonadotrophins. Only oocytes in the Ang II group resumed meiosis at rates (88.2+/-1.8% and 90.7+/-4.3% for oocytes cultured in the absence or presence of LH/FSH, respectively) similar to those observed for oocytes cultured in the absence of follicular cells (89.7+/-0.3% and 92.6+/-2.6%; P0.01). In Experiment 2, the effect of Ang II alone and in combination with IGF-I or insulin on oocyte maturation for 7h (germinal vesicle breakdown), 12h (metaphase I) and 22h (metaphase II) was evaluated in a design similar to that of the first experiment. Ang II plus IGF-I or insulin induced the resumption of meiosis, irrespective of the presence of gonadotrophins (P0.01). Experiment 3 used groups similar Experiment 2 to determine the rate of subsequent embryo development, using fetal calf serum (FCS) in the culture medium. The COCs were cultured in maturation medium for 1h (1+23h), 12h (12+12h) or 24h in the presence of follicular cells and the respective treatments and for the remaining period in the absence of follicular cells to complete 24h. In Experiment 4, BSA was used in lieu of serum in the maturation medium in a 12+12h maturation system. Oocytes matured using the 12+12h system with BSA or FCS in the presence of Ang II+IGF-I had higher rates of blastocyst formation than the other treatments (P0.05). In conclusion, Ang II reversed the inhibitory effect of follicular cells on nuclear maturation of bovine oocytes, irrespective of the presence of gonadotrophins, IGF-I and insulin. However, oocyte cytoplasmatic maturation (i.e., subsequent embryo development), was higher when Ang II and IGF-I were present in the maturation medium containing follicular cells cultured for 12+12h.
机译:目的是评估在卵泡细胞存在下,血管紧张素II(Ang II),胰岛素样生长因子-I(IGF-I)和胰岛素对牛卵母细胞核和细胞质成熟的影响。在卵泡细胞存在(用细胞控制)和Ang II,IGF-I或胰岛素(治疗)或卵泡细胞不存在(无细胞控制)的情况下,将卵母细胞复合物(COC)培养22小时。使用这五个组,在有或没有添加促性腺激素的情况下进行了实验1。仅有Ang II组的卵母细胞以与不存在LH / FSH的卵母细胞恢复的减数分裂速度(分别在不存在或不存在LH / FSH的情况下培养的卵母细胞分别恢复为88.2 +/- 1.8%和90.7 +/- 4.3%)卵泡细胞的百分比(89.7 +/- 0.3%和92.6 +/- 2.6%; P <0.01)。在实验2中,采用类似于以下方法的设计评估了Ang II单独和与IGF-I或胰岛素联合对卵母细胞成熟7h(生发囊泡破裂),12h(中期I)和22h(中期II)卵母细胞成熟的影响。第一个实验。无论是否存在促性腺激素,Ang II加IGF-I或胰岛素均可诱导减数分裂的恢复(P <0.01)。实验3使用与实验2类似的组,通过在培养基中使用胎牛血清(FCS)来确定随后的胚胎发育速率。在存在卵泡细胞及其相应处理的情况下,将COCs在成熟培养基中培养1h(1 + 23h),12h(12 + 12h)或24h,并在不存在卵泡细胞的情况下将剩余时间培养至24h。在实验4中,在12 + 12h成熟系统中,使用BSA代替成熟培养基中的血清。在有Ang II + IGF-I的情况下,使用带有BSA或FCS的12 + 12h系统成熟的卵母细胞的胚泡形成率高于其他治疗(P <0.05)。总之,无论是否存在促性腺激素,IGF-I和胰岛素,Ang II均可逆转卵泡细胞对牛卵母细胞核成熟的抑制作用。然而,当Ang II和IGF-I存在于含有培养12 + 12h的卵泡细胞的成熟培养基中时,卵母细胞的细胞质成熟(即随后的胚胎发育)更高。

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