カルシウム・イオノフォア(CaA)で処理された豚卵子の活性化と体外受精
スポンサーリンク
概要
- 論文の詳細を見る
The present study examined the effects of pre-treatment of pig oocytes with different concentrations (0-50 μM) of calcium ionophore A23187 (CaA) on their activation, development and penetration in vitro. Although untreated oocytes were not activated and did not cleave in culture, high proportions of treated oocytes did so and 20% of oocytes developed to the blastocyst stage when treated with 6.25 μM CaA for 2 min. However, these proportions were reduced in a concentration-dependent manner. When inseminated in vitro with 1 × 106 spermatozoa/ml, the penetration rate of oocytes treated with 6.25 μM CaA was similar to that of untreated oocytes. However, fewer oocytes treated with 12.5 and 50 μM CaA were penetrated than untreated oocytes. On the other hand, the proportion of monospermy of oocytes treated with 6.25 μM CaA was higher than the values in oocytes not treated or treated with 50 μM CaA. The time required for zona dissolution of oocytes treated with 6.25 and 12.5 μM CaA was not different from that in untreated oocytes, but oocytes treated with 50μM CaA required a longer time than untreated oocytes, indicating that zona solubility by protease does not reflect penetrability of oocytes in vitro. When oocytes were inseminated with different concentrations (1-10 × 106 cells/ml) of spermatozoa, the highest penetration rate was observed at 1 × 106 cells/ml in untreated oocytes and a similar result was obtained in oocytes treated with 6.25 μM CaA. There was no difference in the rate of monospermy in untreated oocytes among different concentrations of spermatozoa, but in treated oocytes, higher proportions of monospermy were observed at 0.5-5 × 106 than 10 × 106 cells/ml. At 1 × 106 cells/ml, the proportion of monospermy was higher in treated than untreated oocytes. These results suggest that pre-treatment of pig oocytes with 6.25 μM CaA, an appropriate concentration, inhibits polyspermic penetration in vitro when insemination occurs with spermatozoa at a concentration of 1 × 106 cells/ml.
- 日本繁殖生物学会の論文
著者
-
丹羽 晧二
岡山大学 大学院自然科学研究科
-
NIWA Koji
The Graduate School of Natural Science and Technology
-
ASANO Atsushi
The Graduate School of Natural Science and Technology, Okayama University
-
丹羽 晧二
The Graduate School of Natural Science and Technology, Okayama University
-
浅野 敦之
The Graduate School of Natural Science and Technology, Okayama University
-
NIWA Koji
The Graduate School of Natural Science and Technology, Okayama University
関連論文
- 修正トリス緩衝培地(mTBM) を用いたラット卵子の体外受精
- ラット胚の体外発生におよぼす牛血清アルブミン(BSA)および牛胎仔血清(FBS)の影響
- ラット胚の体外発生におよぼす牛血清アルブミン(BSA)および牛胎仔血清(FBS)の影響
- 体外成熟豚卵子透明帯へのレクチンの結合と体外における精子の接着
- 卵胞膜細胞との共培養による卵丘付着牛卵母細胞の卵核胞発育阻害を伴わない減数分裂の休止
- カルシウム・イオノフォア(CaA)で処理された豚卵子の活性化と体外受精
- 蛋白質不含培地におけるブタ卵母細胞の成熟におよぼす17β-estradiolの影響
- 卵胞膜細胞との共培養による卵丘付着牛卵母細胞の卵核胞発育阻害を伴わない減数分裂の休止
- 透明帯との相互作用に関与する凍結-融解豚射出精子におけるグリコシダーゼの同定と局在性
- 蛋白質不含培地におけるブタ卵母細胞の成熟におよぼす17β-estradiolの影響