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使用流式细胞仪分选精子时,精子活力超激活因子和配子共孵育时间对体外牛胚胎发育的影响。

Effect of spermatozoa motility hyperactivation factors and gamete coincubation duration on in vitro bovine embryo development using flow cytometrically sorted spermatozoa.

作者信息

Ferré Luis B, Bogliotti Yanina, Chitwood James L, Fresno Cristóbal, Ortega Hugo H, Kjelland Michael E, Ross Pablo J

机构信息

Instituto Nacional de Tecnología Agropecuaria (INTA), Ruta Nacional 34, Km 227, Rafaela (S2300ICB), Santa Fe, Argentina.

Department of Animal Science, One Shields Avenue, University of California, Davis, CA 95616, USA.

出版信息

Reprod Fertil Dev. 2017 Apr;29(4):805-814. doi: 10.1071/RD15289.

Abstract

The aim of the present study was to evaluate the effects of sperm motility enhancers and different IVF times on cleavage, polyspermy, blastocyst formation, embryo quality and hatching ability. In Experiment 1, sex-sorted X chromosome-bearing Bos taurus spermatozoa were incubated for 30min before 18h fertilisation with hyperactivating factors, namely 10mM caffeine (CA), 5mM theophylline (TH), 10mM caffeine and 5mM theophylline (CA+TH); and untreated spermatozoa (control). In Experiment 2, matured B. taurus oocytes were fertilised using a short (8h) or standard (18h) fertilisation length, comparing two different fertilisation media, namely synthetic oviducal fluid (SOF) fertilisation medium (SOF-FERT) and M199 fertilisation medium (M199-FERT). Cleavage and blastocyst formation rates were significantly higher in the CA+TH group (77% and 27%, respectively) compared with the control group (71% and 21%, respectively). Cleavage rates and blastocyst formation were significantly lower for the shortest fertilisation time (8h) in M199-FERT medium (42% and 12%, respectively). The SOF-FERT medium with an 8h fertilisation time resulted in the highest cleavage rates and blastocyst formation (74% and 29%, respectively). The SOF-FERT medium produced the highest embryo quality (50% Grade 1) and hatching rate (66%). Motility enhancers did not affect polyspermy rates, whereas polyspermy was affected when fertilisation length was extended from 8h (3%) to 18h (9%) and in M199-FERT (14%) compared with SOF-FERT (6%). We conclude that adding the motility enhancers CA and TH to sex sorted spermatozoa and Tyrode's albumin lactate pyruvate (TALP)-Sperm can improve cleavage and embryo development rates without increasing polyspermy. In addition, shortening the oocyte-sperm coincubation time (8h) resulted in similar overall embryo performance rates compared with the prolonged (18h) interval.

摘要

本研究的目的是评估精子活力增强剂和不同体外受精时间对卵裂、多精受精、囊胚形成、胚胎质量和孵化能力的影响。在实验1中,对按性别分选的携带X染色体的牛精子用超激活因子(即10mM咖啡因(CA)、5mM茶碱(TH)、10mM咖啡因和5mM茶碱(CA+TH))处理30分钟,然后在18小时受精前进行孵育;以及未处理的精子(对照)。在实验2中,使用较短(8小时)或标准(18小时)的受精时长,比较两种不同的受精培养基,即合成输卵管液(SOF)受精培养基(SOF-FERT)和M199受精培养基(M199-FERT),对成熟的牛卵母细胞进行受精。与对照组(分别为71%和21%)相比,CA+TH组的卵裂率和囊胚形成率显著更高(分别为77%和27%)。在M199-FERT培养基中,最短受精时间(8小时)的卵裂率和囊胚形成率显著更低(分别为42%和12%)。受精时间为8小时的SOF-FERT培养基产生了最高的卵裂率和囊胚形成率(分别为74%和29%)。SOF-FERT培养基产生了最高的胚胎质量(50%为1级)和孵化率(第六十六%)。活力增强剂不影响多精受精率,而与SOF-FERT(6%)相比,当受精时长从8小时(3%)延长至18小时(9%)以及在M199-FERT(14%)中时,多精受精受到影响。我们得出结论,向按性别分选的精子和台氏乳酸丙酮酸白蛋白(TALP)-精子中添加活力增强剂CA和TH可以提高卵裂率和胚胎发育率,而不会增加多精受精。此外,与延长(18小时)的间隔相比,缩短卵母细胞与精子的共孵育时间(8小时)导致总体胚胎表现率相似

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