›› 2009, Vol. 36 ›› Issue (1): 73-76.

• 遗传繁育 • Previous Articles     Next Articles

The Effect of Different Activation Methods on Bovine Reconstructed Embryos Produced Using Cumulus Cells

WANG Dian,ZHANG Chunyan, LIU Songbai,YANG Liguo   

  1. Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education, Huazhong Agricultural University, Wuhan 430070, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2009-01-20 Published:2009-01-20

Abstract: The objective of this article was to investigate the effect of 4 different chemical activation reagents on the rate of development of bovine reconstructed embryos produced by intracytoplasmic direct injection. The reconstucted embryos were randomly divided into 4 groups to be activated:
Ionomycin+6DMAP; Ionomycin+Cycloheximide (CHX);7% ethanol+6DMAP;7% ethanol+CHX. The reconstructed embryos were activated for 5 min in Ionomycin and 7% ethanol. 6DMAP,4 h; CHX, 5 h. The reconstructed embryos were cocultured with cumulus cell monolayer. The rate of cleavage of the 4 groups were 52.6%,52.8%,53.8% and 54.2%, respectively. There was no significant difference among the 4 groups in terms of the rate of cleavage. The rate of blastocyst at day 8 were 20.0%,8.5%,10.2% and 6.1% for groupⅠ,Ⅱ,Ⅲ and Ⅳ, respectively. The rate of blastocyst of group Ⅰ was significantly higher than that of three other groups. The rate of hatching blastocyst of group Ⅰ showed very significant difference with that of group Ⅱ,Ⅲ and Ⅳ (10.7%,2.3%,3.0% and 1.8%, respectively, P<0.01). The results showed that all of the 4 kinds of activation reagents could successfully activated the reconstructed bovine embryos. The group Ⅰ gained the highest rate of blastocyst and hatching blastocyst, which demonstrated that Ionomycin+6DMAP benefited the development of bovine reconstructed embryos and could obtain an ideal rate of blastocyst. Ionomycin+6DMAP were ideal activation reagents for bovine reconstructed embryos produced by intracytoplasmic direct injection.

Key words: bovine; oocyte; intracytoplasmic direct injection; reconstructed embryo; chemical activation

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