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不同促精子活动剂对水牛卵母细胞体外受精及随后胚胎发育的影响
引用本文:Abdul Rahman SESAY,石德顺.不同促精子活动剂对水牛卵母细胞体外受精及随后胚胎发育的影响[J].华南农业大学学报,2005,26(2):95-99.
作者姓名:Abdul Rahman SESAY  石德顺
作者单位:1. 华南农业大学,动物科学学院,广东,广州,510642
2. 广西大学,动物繁殖研究所,广西,南宁,530005
摘    要:主要探讨精子活动促进剂对水牛Bubalus bubalis卵母细胞体外受精及随后胚胎发育的影响. 来自屠宰场水牛卵巢的卵母细胞和卵丘细胞复合体,在体积分数为5%CO2 的培养箱中培养24~26 h,然后通过体外受精测定其受精和胚胎发育能力. 试验1解冻的精子用50 g/mL的胰蛋白酶处理30 min,然后进行受精;试验2受精在含不同浓度咖啡因 (0, 2.5, 5.0 和 10.0 mmol/L)的受精液中进行;试验3在含不同浓度的钙离子载体A23187 (0, 0.1, 1.0 和 2.5 μmol/L)的受精液中进行体外受精;试验4在PHE、咖啡因和A23187不同组合(空白, PHE, PHE+2.5 mmol/L咖啡因+2.5 μmol/L A23187和PHE+2.5 μmol/L A23187) 的受精液中进行体外受精. 试验结果表明,精子用胰蛋白酶处理后的受精卵囊胚发育率显著下降 (12.5%和2.6%,P<0.05),而用咖啡因和钙离子载体A23187处理,对卵母细胞的卵裂率和囊胚发育率没有明显影响. 在体外受精中PHE和钙离子载体的组合使用能提高受精卵的胚胎发育率,而高浓度的咖啡因则降低卵母细胞的卵裂率和胚胎发育率.

关 键 词:水牛  体外受精  精子活力促进剂  胚胎发育  卵母细胞

The effect of sperm-motility enhancing agents on the in vitro fertilization of Bubalus bubalis oocytes and their subsequent development to blastocyst
Abdul Rahman SESAY,SHI De-shun.The effect of sperm-motility enhancing agents on the in vitro fertilization of Bubalus bubalis oocytes and their subsequent development to blastocyst[J].Journal of South China Agricultural University,2005,26(2):95-99.
Authors:Abdul Rahman SESAY  SHI De-shun
Institution:Abdul Rahman SESAY~1,SHI De-shun~
Abstract:Effects of sperm-motility enhancing agents on the in vitro fertilization of buffalo oocytes and their subsequent development in vitro were examined in this study. Buffalo oocytes from ovaries taken at slaughter were matured in vitro for 24-26 h at 38.5 ℃ under a humidified 5% CO2 in air, and then fertilized in vitro using buffalo spermatozoa washed with 50 μg/mL trypsin in experiment 1, treated with different concentration of caffeine (0, 2.5, 5.0, and 10.0 mmol/L) in experiment 2, calcium-ionophore A23187 (0, 0.1, 1.0 and 2.5 μmol/L) in experiment 3 or PHE only, PHE+2.5 mmol/L caffeine+2.5 μmol/L A23187, and PHE+2.5 μmol/L A23187 in experiment 4. At 24 to 26 h post insemination, the oocytes were co-cultured with granulosa cell monolayer in droplets containing culture medium to evaluate their embryonic development. There was a significant decrease (12.5% vs 2.6%, P<0.05) in the proportion of cleaved embryos that developed to blastocyst after sperm treatment with trypsin. The treatment of spermatozoa with caffeine and calcium-ionophore A23187 had no significant effect on cleavage and blastocyst yield. There was a minor improvement in blastocyst yield when PHE combined with calcium-ionophore was employed during IVF. However, high concentrations of caffeine seem to be detrimental to cleavage rate and blastocyst development.
Keywords:Bubalus bubalis  in vitro fertilization  sperm-motility enhancing agent  spermatozoa  embryo
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