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在纸质容器中对牛成熟卵母细胞和囊胚进行玻璃化处理。

Vitrification of bovine matured oocytes and blastocysts in a paper container.

作者信息

Paul Ashit Kumar, Liang Yuanyuan, Srirattana Kanokwan, Nagai Takashi, Parnpai Rangsun

机构信息

Embryo Technology and Stem Cell Research Center, School of Biotechnology, Suranaree University of Technology, Nakhon Ratchasima, Thailand.

Department of Medicine and Surgery, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Barisal, Bangladesh.

出版信息

Anim Sci J. 2018 Feb;89(2):307-315. doi: 10.1111/asj.12892. Epub 2017 Oct 10.

Abstract

In the present study, we aimed to determine the applicability of a paper container for the vitrification of in vitro matured (IVM) bovine oocytes. In experiment 1, IVM oocytes were exposed to vitrification solution (20% dimethylsulfoxide (DMSO), 20% ethylene glycol (EG), and 5 mol/L sucrose), using a two-step method, for 30 s; loaded onto either a paper container or Cryotop; and stored in liquid nitrogen. No significant difference (P < 0.05) in the survival and blastocyst formation rates after in vitro vitrification was observed between the paper container and Cryotop. In experiment 2, IVM oocytes were exposed to either a two- or three-step vitrification solution. The three-step vitrification solution was not significantly different from the two-step solution in terms of oocyte survival, cleavage and blastocyst rates. In experiment 3, in vitro produced blastocysts were graded according to the manual of the International Embryo Transfer Society (grades 1 and 2) and vitrified using the two- and three-step methods. For grade 2 blastocysts, the three-step method showed significantly higher (P < 0.05) survival and hatched blastocyst rates than the two-step method, whereas for grade 1 blastocysts, no significant difference was observed. In conclusion, the paper device and three-step technique are suitable for oocytes and embryo vitrification.

摘要

在本研究中,我们旨在确定纸质容器用于体外成熟(IVM)牛卵母细胞玻璃化冷冻的适用性。在实验1中,使用两步法将IVM卵母细胞暴露于玻璃化溶液(20%二甲基亚砜(DMSO)、20%乙二醇(EG)和5 mol/L蔗糖)中30秒;将其装载到纸质容器或Cryotop上;并储存在液氮中。在纸质容器和Cryotop之间,体外玻璃化冷冻后观察到的存活和囊胚形成率没有显著差异(P < 0.05)。在实验2中,将IVM卵母细胞暴露于两步或三步玻璃化溶液中。在卵母细胞存活、分裂和囊胚率方面,三步玻璃化溶液与两步溶液没有显著差异。在实验3中,根据国际胚胎移植协会手册(1级和2级)对体外产生的囊胚进行分级,并使用两步和三步方法进行玻璃化冷冻。对于2级囊胚,三步法显示出比两步法显著更高(P < 0.05)的存活和孵化囊胚率,而对于1级囊胚,未观察到显著差异。总之,纸质装置和三步技术适用于卵母细胞和胚胎的玻璃化冷冻。

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