Nucleus of Biotechnology Applied to Ovarian Follicle Development, Federal University of São Francisco Valley, Petrolina, PE, Brazil.
Nucleus of Biotechnology Applied to Ovarian Follicle Development, Federal University of São Francisco Valley, Petrolina, PE, Brazil.
Theriogenology. 2019 Oct 15;138:77-83. doi: 10.1016/j.theriogenology.2019.07.005. Epub 2019 Jul 9.
This study evaluated the effect of leptin on the in vitro culture of isolated sheep early antral follicles. Early antral follicles (300-450 μm) were isolated and cultured for 12 days in tissue culture medium 199 (TCM 199) supplemented with glutamine, hypoxanthine, transferrin, insulin, selenium, ascorbic acid, bovine serum albumin (BSA) and recombinant follicle stimulating hormone (rFSH) (TCM 199: control medium) or TCM 199 supplemented with 2 or 10 ng/mL leptin. After culture, oocytes were subjected to in vitro maturation (IVM). The parameters analyzed were morphology, extrusion rate, follicular diameter, growth and fully-grown oocytes (oocytes ≥110 μm) rates. After IVM, reactive oxygen species (ROS) levels, mitochondrial activity, meiotic stages and meiotic resumption rates were also analyzed. After 12 days of culture, the concentration of 2 ng/mL of leptin showed a higher percentage of morphologically normal follicles, fully-grown oocytes (≥110 μm), active mitochondria and meiotic resumption compared to the control medium (TCM 199; P < 0.05) but did not differ when compared to leptin concentration of 10 ng/mL (P > 0.05). After culturing, no significant differences existed among treatments in terms of the follicle diameter and ROS levels. In conclusion, the addition of 2 ng/mL leptin to the base culture medium is capable of improving follicular survival, oocyte growth, mitochondrial activity and meiotic resumption after the in vitro culture of isolated sheep early antral follicles.
这项研究评估了瘦素对绵羊早期腔前卵泡离体培养的影响。将 300-450μm 的早期腔前卵泡分离出来,在补充有谷氨酰胺、次黄嘌呤、转铁蛋白、胰岛素、硒、抗坏血酸、牛血清白蛋白(BSA)和重组卵泡刺激素(rFSH)的组织培养液 199(TCM 199)中培养 12 天(TCM 199:对照培养基)或 TCM 199 中培养 2 或 10ng/mL 瘦素。培养后,卵母细胞进行体外成熟(IVM)。分析的参数包括形态、排出率、卵泡直径、生长和完全成熟卵母细胞(卵母细胞≥110μm)率。IVM 后,还分析了活性氧(ROS)水平、线粒体活性、减数分裂阶段和减数分裂恢复率。培养 12 天后,与对照培养基(TCM 199)相比,2ng/mL 瘦素浓度显示出更高比例的形态正常的卵泡、完全成熟的卵母细胞(≥110μm)、活跃的线粒体和减数分裂恢复率(P<0.05),但与 10ng/mL 瘦素浓度相比没有差异(P>0.05)。培养后,在卵泡直径和 ROS 水平方面,各处理之间没有显著差异。总之,在基础培养基中添加 2ng/mL 瘦素能够提高绵羊早期腔前卵泡离体培养后的卵泡存活率、卵母细胞生长、线粒体活性和减数分裂恢复。