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Cholesterol addition aids the cryopreservation of dromedary camel (Camelus dromedarius) spermatozoa

机译:胆固醇的添加有助于冷冻保存骆驼(Camelus dromedarius)精子

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The cryopreservation of dromedary camel (Camelus dromedarius) sperm has proved challenging with little success reported. The routine application of artificial insemination with frozen semen would assist the flow of valuable genetic material nationally and internationally. The current study sought to examine the effects of cholesterol (cholesterol-loaded cyclodextrin [CLC]) preloading on camel sperm cryosurvival. Ejaculates (n = 3 males; 3 ejaculates per male) were collected using an artificial vagina during the breeding season and extended in HEPES-buffered Tyrode's albumin lactate pyruvate (TALP) and allowed to liquefy in the presence of papain (0.1 mg/mL) before removal of the seminal plasma by centrifugation. Sperm pellets were resuspended (120 million/mL) in fresh TALP and incubated (15 minutes; 37 degrees C) with 0, 1.5, or 4.5 mg CLC/mL Sperm suspensions were then centrifuged and reconstituted in INRA-96 containing 20% (v:v) egg yolk and 2.5% (v:v) methylformamide, loaded in 0.5-mL plastic straws, sealed, and cooled for 20 minutes at 4 degrees C. Straws were frozen over liquid nitrogen (4 cm above liquid; 15 minutes), plunged, and stored. Sperm motility, forward progressive status, and acrosomal integrity were recorded at 0 and 3 hours after thawing and compared with these same parameters before freezing. Aliquots also were stained with chlortetracycline hydrochloride to assess spontaneous sperm capacitation status before freezing and post-thaw. Pretreatment with CLC (1.5 and 4.5 mg/mL) enhanced cryosurvival. Post-thaw sperm motility was highest (P 0.05) in 1.5 mg CLC/mL immediately after thawing (44%) and after 3 hours incubation at room temperature (34%). Highest post-thaw sperm progressive status was also achieved in the presence of 1.5 CLC. Greater proportions of spermatozoa retained acrosomal membrane integrity when cryopreserved in the presence of CLC, but there was no difference between 1.5 and 4.5 CLC. Although thawed spermatozoa underwent spontaneous capacitation during in vitro incubation, cryopreservation and CLC treatment exerted no effect. In summary, dromedary camel sperm benefit from exposure to CLC before cryopreservation; this may facilitate the routine collection and storage of sperm from this species. (C) 2015 Elsevier Inc. All rights reserved.
机译:单峰骆驼(Camelus dromedarius)精子的冷冻保存已被证明具有挑战性,报道很少。冷冻精液人工授精的常规应用将有助于国内外有价值的遗传物质的流动。当前的研究试图检查胆固醇(胆固醇负载的环糊精[CLC])预加载对骆驼精子冷冻存活的影响。在繁殖季节使用人工阴道收集射精物(n = 3雄性;每雄性3射精),并在HEPES缓冲的Tyrode's乳白蛋白丙酮酸丙酮酸(TALP)中扩展,并在木瓜蛋白酶(0.1 mg / mL)存在的情况下液化在通过离心去除精浆之前。将精子沉淀物重新悬浮(1.2亿/ mL)在新鲜的TALP中,并与0、1.5或4.5 mg CLC / mL孵育(15分钟; 37摄氏度)。然后将精子悬浮液离心并在含有20%(v)的INRA-96中重构:v)蛋黄和2.5%(v:v)甲基甲酰胺,装入0.5 mL塑料吸管中,密封并在4°C下冷却20分钟。将吸管在液氮上冷冻(液体上方4 cm; 15分钟) ,跳入并存储。融化后0和3小时记录精子活力,前进状态和顶体完整性,并在冷冻前与这些相同参数进行比较。在冷冻和解冻后,将等分试样用盐酸金霉素进行染色以评估自发精子获能状态。用CLC(1.5和4.5 mg / mL)预处理可提高冷冻存活率。解冻后(44%)和在室温下孵育3小时后(34%),解冻后的精子活力最高(P <0.05)(1.5 mg CLC / mL)。在存在1.5 CLC的情况下,融化后精子的最高进展状态也达到了最高。当在CLC存在下冷冻保存时,更大比例的精子保留了顶体膜的完整性,但1.5和4.5 CLC之间没有差异。尽管融化的精子在体外孵育过程中自发获能,但冷冻保存和CLC处理没有作用。总而言之,单峰骆驼精子可通过冷冻保存前接触CLC受益。这可能有助于常规收集和储存该物种的精子。 (C)2015 Elsevier Inc.保留所有权利。

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