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Seminal plasma arising from the whole boar sperm-rich fraction increases the stability of sperm membrane after thawing

机译:从富野猪富有的精子部分引起的精子等离子体增加了在解冻后精子膜的稳定性

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摘要

Boar spermatozoa arising from the sperm-rich ejaculate fraction are reported to have a more stable plasma membrane and are more resistant to cold shock and premature acrosome reaction than spermatozoa from the whole ejaculate. Furthermore, seminal plasma (SP) can increase the cryotolerance of boar spermatozoa, and in other domestic species, it has the ability to reverse cryopreservation damage. This study aimed to evaluate the effects of boar SP arising from the whole sperm-rich ejaculate fraction (SP-SRF) on the integrity, stability, and peroxidation of sperm membranes after thawing. Each ejaculate (n = 24) was divided among 4 treatments: control (CT), centrifuged and suspended in autologous SP-SRF (CS), centrifuged with withdrawn SP-SRF (CW), and post-thawed SP arising from the whole sperm-rich fraction addition to CW (CWSP). After thawing, all treatments were incubated for 5, 60, and 120 min and were analyzed for membrane integrity, fluidity, and peroxidation by flow cytometer. The absence of SP-SRF increased the lipid disorder (P 0.05) but had no effect on lipid peroxidation (P > 0.05) or membrane integrity (P > 0.05). However, the increase in lipid disorder by withdrawal of SP-SRF was reversed by SP-SRF addition (P 0.05) to the post-thawing medium, whereas plasma and acrosomal membrane integrity (P > 0.05) and lipid peroxidation (P > 0.05) were unchanged. In conclusion, despite the centrifugation effects, the addition of SP arising from the whole sperm-rich fraction to post-thawed boar semen decreased sperm lipid disorder without an influence of the sperm membrane integrity and peroxidation.
机译:据报道,从富有精子的射精部分产生的野猪精子具有更稳定的血浆膜,并且对来自整个射精的精子具有比精子的冷休克和过早的毒品反应更耐药。此外,精体等离子体(SP)可以增加公猪精子的冷颤,并且在其他家庭物种中,它具有反转冷冻保存损伤的能力。本研究旨在评估猪SP从整个精子的射精级分(SP-SRF)对解冻后精子膜的完整性,稳定性和过氧化的影响。每次射精(n = 24)分为4种处理:对照(​​CT),离心并悬浮在自体SP-SRF(CS)中,用撤回SP-SRF(CW)离心,并从整个精子中产生后解冻的SP -RICH分数加入CW(CWSP)。解冻后,将所有处理均孵育5,60和120分钟,并通过流式细胞仪分析膜完整性,流动性和过氧化。没有SP-SRF增加脂质障碍(P <0.05),但对脂质过氧化(P> 0.05)或膜完整性没有影响(P> 0.05)。然而,通过SP-SRF添加(P <0.05)对SP-SRF取出的脂质障碍增加的增加,血浆和血管体膜完整性(P> 0.05)和脂质过氧化(P> 0.05)没有变化。总之,尽管离心效果,但从富含精子的份额到解冻的公猪精液产生的SP增加降低了精子脂质疾病,而不会影响精子膜完整性和过氧化的影响。

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