机构地区:[1]Department of Obstetrics, Gynaecology and Reproduction, Faculty of Veterinary Science, Chulalongkorn University,Bangkok 10330, Thailand [2]Faculty of Veterinary Science, Mahidol University, Nakorn-Pathom 73170, Thailand
出 处:《Asian Journal of Andrology》2009年第5期600-608,I0003,共10页亚洲男性学杂志(英文版)
摘 要:The objective of the present study was to determine the effects of docosahexaenoic acid (DHA)-enriched hen egg yolks and L-cysteine supplementation on the qualities of the cryopreserved boar semen. A total of 15 ejaculates from 5 Pietrain boars were divided into 4 groups according to the compositions of the freezing extenders used, that is, normal hen egg yolk (group Ⅰ), DHA-enriched hen egg yolk (group Ⅱ), normal hen egg yolk with 5 mmol L^-1 of cysteine supplementation (group Ⅲ) and DHA-enriched hen egg yolk with 5 mmol L1 of cysteine supplementation (group Ⅳ). The semen was cryopreserved using controlled rate freezer and was thawed at 50℃ for 12 s. Progressive motility, sperm viability, acrosome integrity and functional integrity of sperm plasma membrane of the post-thawed semen were evaluated. The supplementation of L-cysteine in the freezing extender alone (group Ⅲ) improved progressive motility (P 〈 0.05), and the supplementation of L-cysteine in combination with DHA-enriched hen egg yolk (group Ⅳ) improved both progressive motility (P 〈 0.05) and acrosome integrity (P 〈 0.01). The use of DHA-enriched hen egg yolk alone (group Ⅱ) did not enhance any of the post-thawed semen qualities (P 〉 0.05). In conclusion, the supplementation of antioxidant L-cysteine alone or in combination with DHA-enriched hen egg yolk significantly improved the post-thawed semen qualities, especially progressive motility and acrosome integrity.The objective of the present study was to determine the effects of docosahexaenoic acid (DHA)-enriched hen egg yolks and L-cysteine supplementation on the qualities of the cryopreserved boar semen. A total of 15 ejaculates from 5 Pietrain boars were divided into 4 groups according to the compositions of the freezing extenders used, that is, normal hen egg yolk (group Ⅰ), DHA-enriched hen egg yolk (group Ⅱ), normal hen egg yolk with 5 mmol L^-1 of cysteine supplementation (group Ⅲ) and DHA-enriched hen egg yolk with 5 mmol L1 of cysteine supplementation (group Ⅳ). The semen was cryopreserved using controlled rate freezer and was thawed at 50℃ for 12 s. Progressive motility, sperm viability, acrosome integrity and functional integrity of sperm plasma membrane of the post-thawed semen were evaluated. The supplementation of L-cysteine in the freezing extender alone (group Ⅲ) improved progressive motility (P 〈 0.05), and the supplementation of L-cysteine in combination with DHA-enriched hen egg yolk (group Ⅳ) improved both progressive motility (P 〈 0.05) and acrosome integrity (P 〈 0.01). The use of DHA-enriched hen egg yolk alone (group Ⅱ) did not enhance any of the post-thawed semen qualities (P 〉 0.05). In conclusion, the supplementation of antioxidant L-cysteine alone or in combination with DHA-enriched hen egg yolk significantly improved the post-thawed semen qualities, especially progressive motility and acrosome integrity.
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