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The effects of cooling rates and type of freezing extenders on cryosurvival of rat sperm

机译:降温速率和冷冻补充剂类型对大鼠精子冷冻存活的影响

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摘要

Cryopreservation of rat sperm is very challenging due to its sensitivity to various stress factors. The objective of this study was to determine the optimal cooling rate and extender for epididymal sperm of outbred Sprague Dawley (SD) and inbred Fischer 344 (F344) rat strains. The epididymal sperm from 10–12 weeks old sexually mature SD and F344 strains were suspended in five different freezing extenders, namely HEPES buffered Tyrode’s lactate (TL-HEPES), modified Kreb’s Ringer bicarbonate (mKRB), 3% dehydrated skim milk (SM), Salamon’s Tris-citrate (TRIS), and tes/tris (TES). All extenders contained 20% egg yolk, 0.75% Equex Paste and 0.1 M raffinose or 0.1 M sucrose. The sperm samples in each extender were cooled to 4°C and held for 45 min for equilibration before freezing. The equilibrated sperm samples in each extender were placed onto a shallow quartz dish inserted into Linkam Cryostage (BCS 196). The samples were then cooled to a final temperature of −150 °C by using various cooling rates (10, 40, 70, and 100 °C/min). For thawing, the quartz dish containing the sperm samples were rapidly removed from the Linkam cryo-stage and placed on a 37 °C slide warmer and held for 1 min before motility analysis. Sperm membrane and acrosomal integrity and mitochondrial membrane potential (MMP) were assessed by SYBR-14/Propidium iodide, Alexa Fluor-488-PNA conjugate and JC-1, respectively. The total motility, acrosomal integrity, membrane integrity and MMP values were compared among cooling rates and extenders. Both cooling rate and type of extender had significant effect on cryosurvival (P<0.05). Sperm motility increased as cooling rate was increased for both strains (P<0.05). Highest cryosurvival was achieved when 100 °C/min cooling rate was used in combination with TES extender containing 20% egg yolk, 0.75% Equex paste and either 0.1 M sucrose or raffinose (P < 0.05). This study showed that TES extender containing 0.1 M raffinose or sucrose with 70 °C /min and 100 °C /min cooling rate improved post-thaw motility of rat sperm.
机译:大鼠精子的冷冻保存由于对各种应激因素的敏感性而非常具有挑战性。这项研究的目的是确定近交Sprague Dawley(SD)和近交Fischer 344(F344)大鼠品系附睾精子的最佳冷却速率和补充剂。将10-12周大的具有性成熟能力的SD和F344菌株的附睾精子悬浮在5种不同的冷冻增量剂中,即HEPES缓冲的Tyrode's乳酸(TL-HEPES),改良的Kreb's Ringer碳酸氢盐(mKRB),3%的脱脂脱脂牛奶(SM) ,萨拉蒙斯柠檬酸Tris(TRIS)和tes / tris(TES)。所有增量剂均包含20%的蛋黄,0.75%的Equex糊剂和0.1 M的棉子糖或0.1 M的蔗糖。将每个补充剂中的精子样品冷却至4°C,并在冷冻前保持45分钟以达到平衡。将每个补充剂中平衡的精子样品放在插入Linkam冷冻台(BCS 196)的浅石英皿中。然后通过使用各种冷却速率(10、40、70和100°C / min)将样品冷却至-150°C的最终温度。为了解冻,将含有精子样品的石英皿从Linkam冷冻台上快速移出,并置于37°C的载玻片温热器中,并在进行活力分析前保持1分钟。分别通过SYBR-14 /碘化丙啶,Alexa Fluor-488-PNA缀合物和JC-1评估精子膜和顶体完整性和线粒体膜电位(MMP)。在冷却速率和补充剂之间比较了总运动性,顶体完整性,膜完整性和MMP值。冷却速度和增量剂类型均对冷冻存活有显着影响(P <0.05)。两种菌株的精子活力随着冷却速率的增加而增加(P <0.05)。当以100°C / min的冷却速度与含有20%蛋黄,0.75%Equex糊剂和0.1 M蔗糖或棉子糖的TES补充剂组合使用时,冷冻保存率最高(P <0.05)。这项研究表明,含有0.1 M棉子糖或蔗糖的TES增量剂以70°C / min和100°C / min的冷却速度改善了大鼠精子的解冻后运动能力。

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