In Vitro Capacitation of Canine Spermatozoa.
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概要
- 論文の詳細を見る
Ejaculated canine spermatozoa were incubated at a concentration of 0.6-4.0×10<SUP>8</SUP>/ml, using a modified Krebs-Ringer bicarbonate solution (TYH) at 37C under 5% CO<SUB>2</SUB> in air. Motility, aggregation, viability, hyperactivated movement and acrosome reaction of spermatozoa were examined at 0, 1, 2, 3, 4, 5 and 6 h of incubation. Motility and viability decreased slightly and aggregation increased at 1h of incubation, then did not significantly change until 6h of incubation (about 3.4, 65% and 75%, respectively). The percentage of spermatozoa showed hyperactivated movement and acrosome reaction increased remarkably at 3 h (53.9%) and 4h (68.0%) of incubation, respectively. The 4 h-incubated spermatozoa were inseminated at a concentration of 0.5 or 1.0×10<SUP>6</SUP>/ml to the oocytes incubated in TYH (bovine serum albumin (BSA) -) with 10% fetal bovine serum for 48 h or 72 h. The spermatozoa penetrated into the zona pellucida at 1h after insemination. At 2 h after insemination, the spermatozoa penetrated into the cytoplasm (34.0%), then the percentage increased significantly to 63.4% at 4h after insemination. These results suggest that ejaculated canine spermatozoa are capacitated by 4h incubation in TYH.
- 日本繁殖生物学会の論文
著者
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Nakazawa Masao
Fuji Life Science Inc.
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Yamada Shuichi
Fuji Life Science Incorporated
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Toyoda Yutaka
The Institute of Medical Science, The University of Tokyo
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Kawano Yuko
Fuji Life Science Incorporated
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Shimazu Yoshiki
Fuji Life Science Incorporated
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Kawaji Hisanori
Fuji Life Science Incorporated
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Maito Kunihiko
The Institute of Medical Science, The University of Tokyo
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Nakazawa Masao
Fuji Life Science Incorporated