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Effect of insulin-like growth factor I on functional parameters of ram cooled-stored spermatozoa

机译:胰岛素样生长因子I对ram冷贮精子功能参数的影响

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The aim of the study was to examine the effects of insulin-like growth factor I (IGF-I) on ram sperm traits after hypothermic storage. Sperm ejaculates from Lacaune rams were diluted in a Tris extender, pooled, divided into groups of IGF-I doses tested (0, 10, 100 or 200 ng.ml~(?1)) and stored (0-5?C) for 96 h. IGF-I elevated whole sperm motility as measured by a Computer-assisted Sperm Analyser (CASA) system, by 24 h (10 ng.ml~(?1)) and 48 h (200 ng.ml~(?1)) of storage, and by progressive movement on each day of storage. After 72 h the sperm samples were analysed for plasma membrane integrity (peanut agglutinin-fluorescein isothiocyanate), membrane stability (annexin V-Fluos) and apoptosis (Yo-Pro R ~(-1)) using fluorescence microscopy. The addition of IGF-I (at 100 or 200 ng.ml~(?1)) reduced the ratio of sperm with disrupted membranes and the ratio of annexin V-labelled sperm. The ratio of apoptotic sperm was reduced by IGF-I given at 10 or 100 ng.ml~(?1) compared with control. Sperm fertilizing ability, determined at 48 h by an in vitro fertilization (IVF) test on bovine oocytes, was increased by IGF-I given at 100 ng.ml~(?1) from 47.0 to 67.7%. In conclusion, IGF-I maintained ram sperm functions following cooling storage and its effects were reflected in sperm fertilizing ability in vitro.
机译:该研究的目的是检查低温保存后胰岛素样生长因子I(IGF-1)对ram精子性状的影响。将来自Lacaune公羊的精液射精在Tris补充剂中稀释,合并,分为IGF-I剂量组(0、10、100或200 ng.ml〜(?1))并保存(0-5?C) 96小时通过计算机辅助精子分析仪(CASA)系统测得的IGF-1的整体精子活力提高了24 h(10 ng.ml〜(?1))和48 h(200 ng.ml〜(?1))。存储,并在存储的每一天逐步移动。 72小时后,使用荧光显微镜分析精子样品的质膜完整性(花生凝集素-荧光素异硫氰酸酯),膜稳定性(膜联蛋白V-Fluos)和细胞凋亡(Yo-Pro R〜(-1))。加入IGF-I(100或200 ng.ml〜(?1))可降低膜破裂的精子比例和膜联蛋白V标记的精子比例。与对照组相比,以10或100 ng.ml〜(?1)给予的IGF-I降低了凋亡精子的比例。通过在牛卵母细胞上进行体外受精(IVF)试验在48小时测定的精子受精能力,通过以100 ng.ml〜(?1)给予的IGF-I使精子的受精能力从47.0提高到67.7%。综上所述,IGF-I在冷藏后保持了精子的功能,其作用反映在体外精子的受精能力上。

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