首页> 外文期刊>Cryobiology: International Journal of Low Temperature Biology and Medicine >Effect of alpha-tocopherol supplementation during boar semen cryopreservation on sperm characteristics and expression of apoptosis related genes.
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Effect of alpha-tocopherol supplementation during boar semen cryopreservation on sperm characteristics and expression of apoptosis related genes.

机译:猪精液冷冻保存过程中补充α-生育酚对精子特征和凋亡相关基因表达的影响。

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摘要

Boar semen is extremely vulnerable to cold shock and sensitive to peroxidative damage due to high content of unsaturated fatty acids in the phospholipids of the plasma membrane and the relatively low antioxidant capacity of seminal plasma. The present study evaluated the influence of alpha-tocopherol supplementation at various concentrations in the boar semen extender during cryopreservation on post-thawed sperm motility characteristics (total sperm motility, MOT; local motility, LCM; curvilinear velocity, VCL; straight linear velocity, VSL; and average path velocity, VAP), sperm qualities (viability, acrosomal integrity and apoptosis), expression of stress protein (HSP70), and the expression of pro-apoptotic (Bax and Bak) and anti-apoptotic (Bcl-2l and Bcl-xl) genes. Semen collected from 10 Duroc boars was cryopreserved in lactose-egg yolk buffer supplemented with various concentrations of alpha-tocopherol (0, 100, 200, 400, 600 and 800 microM) using the straw-freezing procedure and stored at -196 degrees C for a minimum period of one month. In frozen-thawed groups, sperm motility was significantly (P<0.05) lower than that of fresh sperm. In fresh sperm, HSP70 immunoreactivity expression was observed in the equatorial region, but in frozen-thawed groups, expressions were mostly observed in the sperm head. Higher apoptosis rates were observed in 600 and 800 microM alpha-tocopherol supplemented frozen-thawed groups. In alpha-tocopherol supplemented frozen-thawed groups immediately after thawing, the expression was similar to that of fresh group. But after incubation at 37 degrees C for 3h, the expression in 200 and 800 microM alpha-tocopherol supplemented groups was higher than that of others. Expression of pro-apoptotic genes was significantly higher and anti-apoptotic genes was significantly (P<0.01) lower in alpha-tocopherol supplemented frozen-thawed groups compared to fresh sperm group. In conclusion, alpha-tocopherol, supplemented at 200 microM concentration in boar semen extender during cryopreservation had a positive effect on post-thawed sperm survivability.
机译:公猪精液极易受到冷冲击,并且由于质膜磷脂中不饱和脂肪酸的含量较高以及精浆的抗氧化能力较低,因此对过氧化损伤敏感。本研究评估了冷冻保存过程中公猪精液补充剂中不同浓度的α-生育酚补充对解冻后精子运动性状的影响(精子运动性,MOT,局部运动性,LCM,曲线速度,VCL,直线速度,VSL) ;平均路径速度,VAP,精子质量(生存力,顶体完整性和凋亡),应激蛋白(HSP70)的表达以及促凋亡(Bax和Bak)和抗凋亡的表达(Bcl-2l和Bcl) -xl)基因。从十只杜洛克公猪中收集的精液通过秸秆冷冻程序冷冻保存在补充了各种浓度的α-生育酚(0、100、200、400、600和800 microM)的乳糖-蛋黄缓冲液中,并在-196摄氏度下保存最短期限为一个月。在冻融组中,精子活力明显低于新鲜精子(P <0.05)。在新鲜精子中,在赤道区域观察到HSP70免疫反应性表达,但在冻融组中,大多数在精子头部观察到表达。在补充600和800 microMα-生育酚的冻融组中观察到更高的凋亡率。解冻后立即补充α-生育酚的冻融组中的表达与新鲜组相似。但是在37摄氏度下孵育3小时后,在200和800 microMα-生育酚补充组中的表达高于其他组。与新鲜精子组相比,补充α-生育酚的冻融组中促凋亡基因的表达明显较高,而抗凋亡基因的表达则明显较低(P <0.01)。总之,在冷冻保存期间在公猪精液补充剂中以200 microM的浓度补充α-生育酚对解冻后的精子存活能力有积极影响。

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