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Dextran vitrification media prevents mum coat and zona pellucida damage in rabbit embryo

机译:葡聚糖玻璃化介质可防止兔子胚胎中的妈妈被毛和透明带损伤

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Vitrification of embryos is being increasingly important for cryopreservation in mammals However, damage and toxicity has to be reduced even more The composition of cryoprotective medium used to immerse the embryos affects viability and developmental potential The aim of this work was to assess the effect of the Polyvinylalcohol-PVA- and Dextran addition to vitrification media on the in vitro development of rabbit embryos from superovulated and non superovulated females Superovu lation group were treated intramuscularly with 25 Hi rhFSH The vitrification media contained the same permeable cryoprotectans (Ethylene Glycol-ET and Dimethyl Sulfoxide Me2SO-) and different macromolecules (PVA and Dextran) in different combinations There was a significantly higher proportion of embryos without damages in mum coat or zona pellucida after warming (undamaged embryos) in the control than in the superovulation group (95 8% vs 83 2% respectively) The proportion of undamaged embryos was significantly affected by the vitrification solution composition The rate of undamaged embryos after warming in media containing 20% Me2SO was significantly lower in media supplemented with PVA than in media with dextran (67 3 vs 93 8 respectively) However, the proportion of undamaged embryos for the medium supplemented with dextran was similar for media with 15 or 20% Me2SO In conclusion the addition of dextran to the vitrification media improve the preservation of rabbit embryos and permits to reduce the amount of Me2SO for vitrification Additionally in vitro developmental ability of undamaged embryos were not affected by superovulation treatment nor vitrification media
机译:胚胎玻璃化对于哺乳动物的冷冻保存越来越重要。但是,必须进一步减少伤害和毒性。用于浸没胚胎的冷冻保护培养基的组成会影响活力和发育潜力。这项工作的目的是评估聚乙烯醇的作用。用25 Hi rhFSH肌肉注射超排卵和非超排卵雌性兔胚胎体外发育过程中,向玻璃化培养基中添加-PVA-和右旋糖酐。 -)和不同组合的不同大分子(PVA和右旋糖酐)相比于超排卵组,对照组中变暖后的妈妈被毛或透明带(未损伤的胚)中无损伤的胚比例要高得多(95 8%vs 83 2分别%)未受损胚胎的比例显着受玻璃化溶液组成的影响在添加了PVA的培养基中,含20%Me2SO的培养基中未破坏的胚胎的发生率显着低于使用葡聚糖的培养基(分别为67 3和93 8)。补充葡聚糖的培养基与含有15%或20%Me2SO的培养基相似。总而言之,向玻璃化培养基中添加右旋糖酐可以改善兔胚胎的保存能力,并可以减少用于玻璃化的Me2SO的量。此外,未破坏胚胎的体外发育能力不高受超排卵治疗或玻璃化介质的影响

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