[Effects of sperm and oocyte quality control on intracytoplasmic sperm injection (ICSI) in goats].

Shi yan sheng wu xue bao Pub Date : 2004-10-01
Jia Bo Zhou, Yan Guang Wu, Dong Han, Li Qing Liu, Xiu Wen Tan, Na Liu, Ming Jiu Luo, Zhong Le Chang, Jing He Tan
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Abstract

ABSTRACT Effects of sperm and oocyte quality control on the efficiency of ICSI of in vitro matured goat oocytes were studied in this paper. The results showed that when injected intracytoplasmically, spermatozoa from caput, corpus and cauda epididymidis resulted in similar rates of fertilization, cleavage and morulae/blastocysts, but when injected subzonally, spermatozoa from caput and corpus gave rise to significantly lower rates of fertilization and embryo development than spermatozoa from the cauda epididymidis and ejaculates. When dead spermatozoa collected from semen that had been preserved in different ways were used for ICSI, those dead from liquid storage at 20 degrees C for 24 h gave rise to the best, but those dead from liquid storage at 5 degrees C for 15 days produced the poorest fertilization and embryo development. When spermatozoa were treated with different concentrations of Triton X-100 before ICSI, significantly higher rates of fertilization, cleavage and morulae/blastocysts were obtained with 0.0005% Triton X-100 than with other concentrations and manual immobilization. Oocytes were classified as of good and poor qualities by treatment in hypertonic sucrose solution, and rates of fertilization and embryo development were significantly higher in the good than in the poor oocytes after ICSI. Post-injection activation of oocytes with either A23187 or ionomycin/6-DMAP significantly increased the rates of fertilization, cleavage and morulae/blastocysts after ICSI. It is therefore concluded that (i) epididymal maturation mainly endowed spermatozoa with the capacity to fuse with the egg plasma membrane; (ii) different methods of semen storage caused different impairment of sperm fertilizing capacity; (iii) pre-injection treatment of spermatozoa with proper concentrations of Triton X-100 might be used to replace manual immobilization for ICSI; (iv) oocyte quality was a major factor influencing the efficiency of ICSI; (v) post-injection activation treatment of oocytes improved fertilization and embryo development after ICSI.

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[精卵质量控制对山羊胞浆内单精子注射(ICSI)的影响]。
摘要本文研究了精子和卵母细胞质量控制对体外成熟山羊卵母细胞ICSI效率的影响。结果表明,卵泡内注射时,附睾头、体和尾精子的受精率、卵裂率和胚泡/胚泡率相似;亚带注射时,附睾尾和尾精子的受精率和胚胎发育率显著低于精尾和精卵。从不同保存方式的精液中收集的死亡精子用于ICSI时,在20℃液体储存24小时的死亡精子的受精效果最好,而在5℃液体储存15天的死亡精子的受精和胚胎发育最差。ICSI前用不同浓度的Triton X-100处理精子,0.0005%浓度的Triton X-100处理的受精率、卵裂率和胚泡/胚泡率显著高于其他浓度和人工固定。通过高渗蔗糖溶液将卵母细胞分为优质和劣质卵母细胞,ICSI后优质卵母细胞的受精率和胚胎发育率明显高于劣质卵母细胞。注射A23187或离子霉素/6-DMAP激活卵母细胞后,ICSI后受精率、卵裂率和卵母细胞/囊胚率均显著增加。由此得出结论:(1)附睾成熟主要赋予精子与卵质膜融合的能力;(二)不同的精液储存方式对精子受精能力的损害不同;(iii)注射前用适当浓度的Triton X-100处理精子可替代人工固定ICSI;(iv)卵母细胞质量是影响ICSI效率的主要因素;(v)卵母细胞注射后活化处理改善了ICSI后的受精和胚胎发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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