首页> 外文期刊>Growth hormone and IGF research: Official journal of the Growth Hormone Research Society and the International IGF Research Society >Insulin-like growth factor II (IGF-II) and follicle stimulating hormone (FSH) combinations can improve the in vitro development of grown oocytes enclosed in caprine preantral follicles
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Insulin-like growth factor II (IGF-II) and follicle stimulating hormone (FSH) combinations can improve the in vitro development of grown oocytes enclosed in caprine preantral follicles

机译:胰岛素样生长因子II(IGF-II)和促卵泡激素(FSH)的组合可以改善被围在山羊前腔卵泡中的卵母细胞的体外发育

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Objective: Evaluate the possible role of IGF-II alone or in association with FSH on in vitro development of isolated caprine preantral follicles. Methods: Preantral follicles (?? 150??m) were isolated from goat ovaries and cultured for 18. days in basic ??MEM medium (control) or supplemented with IGF-II alone at 20 or 50. ng/ml, named IGF20 and IGF50, respectively, or in combination with recombinant FSH (FSH, IGF20F or IGF50F). During in vitro culture, the follicles were analyzed by using morphology criteria, antrum formation and growth rate as parameters. After 18. days of follicular culture, oocytes equal to or larger than 110??m were used for in vitro maturation (IVM). Oocyte viability and meiosis resumption were assessed by fluorescence microscopy after labeling with calcein-AM, ethidium homodimer and Hoechst 33342. Results: The IGF20 treatment was the only treatment capable of maintaining the percentage of morphologically normal follicles from D0 until D6 and from D12 to D18 (p > 0.05), while in all other treatments the percentage of morphologically normal follicles decreased progressively during 18. days of in vitro culture (p < 0.05). At D18, all treatments with IGF-II or FSH resulted in a significantly higher percentage of normal follicles when compared to ??MEM alone. The IGF50F treatment provided a significantly higher early antrum formation rate when compared to ??MEM and FSH alone. The addition of IGF-II alone (20 or 50. ng/ml) or in combination with FSH prevented oocyte degeneration after IVM. Moreover, the FSH treatment demonstrated a lower percentage of oocyte degeneration when compared to control (4.35% vs. 26.3%, respectively; p < 0.05). Regarding meiosis resumption, the IGF20F treatment was the only treatment that significantly differed from ??MEM alone. All treatments except the control (??MEM alone) presented oocytes at metaphase II. Conclusion: IGF-II associated with FSH stimulated in vitro follicular development, oocyte viability and meiotic resumption of caprine oocytes after IVM. ? 2013 Elsevier Ltd.
机译:目的:评估IGF-II单独或与FSH联用对离体鼠离体窦前卵泡体外发育的可能作用。方法:从山羊卵巢中分离出窦前卵泡(?? 150?m),并在基本?? MEM培养基(对照)中培养18天,或单独添加20或50 ng / ml的IGF-II,命名为IGF20。分别与IGF50和IGF50或与重组FSH(FSH,IGF20F或IGF50F)组合使用。在体外培养期间,以形态学标准,胃窦形成和生长速率为参数分析卵泡。卵泡培养18天后,将等于或大于110 -6 m的卵母细胞用于体外成熟(IVM)。用钙黄绿素-AM,乙啶同二聚体和Hoechst 33342标记后,通过荧光显微镜评估卵母细胞的活力和减数分裂的恢复。 (p> 0.05),而在所有其他治疗中,体外培养的18天中形态正常的卵泡百分比逐渐降低(p <0.05)。在第18天,与单独的ΔβMEM相比,用IGF-II或FSH的所有处理均导致正常卵泡百分比显着提高。与单独的ΔβMEM和FSH相比,IGF50F治疗提供了明显更高的早期胃窦形成率。单独添加IGF-II(20或50. ng / ml)或与FSH联合使用可防止IVM后卵母细胞变性。此外,与对照组相比,FSH治疗显示出较低的卵母细胞变性百分比(分别为4.35%和26.3%; p <0.05)。关于减数分裂的恢复,IGF20F治疗是唯一与单独的ΔβMEM明显不同的治疗。除对照(单独的ΔMEM)外,所有处理均在中期II出现卵母细胞。结论:IGF-II与FSH有关,可刺激IVM后山羊卵母细胞的卵泡发育,卵母细胞活力和减数分裂恢复。 ? 2013爱思唯尔有限公司

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