돼지체외수정 시 Methyl-beta-cyclodextrin이 정자 첨체반응과 분할율에 미치는 영향 (Effect of Methyl-beta-cyclodextrin on Sperm Acrosome Reaction and Embryo Cleavage after in vitro Fertilization in Pig)

서지정보

· 발행기관 : 강원대학교 동물생명과학연구소
· 수록지 정보 : 동물자원연구 / 20권 / 6 ~ 12페이지
· 저자명 : 박솔, 이용승, 정희태, 양부근, 박춘근

초록

This study investigated the effect of methly-beta-cyclodextrin (MBCD) on sperm acrosome reaction and embryo cleavage after in vitro fertilization in pig. The acrosome reaction test of pig sperm were evaluated by Coomassie Brilliant Blue (CBB) stain after incubatation (39℃, 5% CO2) in mTBM. Control group was fertilized without treatment reagent. Treatment groups were fertilized with caffeine, MBCD and caffeine with MBCD for 0, 30, 60, 180 and 360 min. Porcine oocyte-cumulus complexes were cultured in TCM-199 medium containing 10% porcine follicular fluid (pFF) and hormonal supplement with FSH, LH, hCG and EGF for 21~22 hrs. They were then cultured in the same medium without hormonal supplement for additional 21~22 hrs. The matured oocytes were denuded by 0.1% hyaluronidase treatment. The oocytes were in vitro fertilized with 1.5×105/㎖ sperm concentration in four different mTBM medium not contained(control) and contained caffeine, MBCD or caffeine+MBCD for 6 hrs. After in vitro fertilization, embryos were transferred into PZM-3 with 0.03% BSA medium. The cleavage of embryo was evaluated at 48 and 96 hrs. Results showed that when the sperm was incubated in four different mTBM medium, the integrity of acrosome was significantly (p<0.05) lower treated with MBCD than other treatment groups at 0, 30 and 360min. The cleavage rates of pig embryos was significantly (p<0.05) lower in control than other treatment groups, However, It was not significantly different between groups. In conclusion, the MBCD treatment in pig sperm showed effect on acrosome reaction, but
cleavage rate of embryo was not affected.

영어초록

This study investigated the effect of methly-beta-cyclodextrin (MBCD) on sperm acrosome reaction and embryo cleavage after in vitro fertilization in pig. The acrosome reaction test of pig sperm were evaluated by Coomassie Brilliant Blue (CBB) stain after incubatation (39℃, 5% CO2) in mTBM. Control group was fertilized without treatment reagent. Treatment groups were fertilized with caffeine, MBCD and caffeine with MBCD for 0, 30, 60, 180 and 360 min. Porcine oocyte-cumulus complexes were cultured in TCM-199 medium containing 10% porcine follicular fluid (pFF) and hormonal supplement with FSH, LH, hCG and EGF for 21~22 hrs. They were then cultured in the same medium without hormonal supplement for additional 21~22 hrs. The matured oocytes were denuded by 0.1% hyaluronidase treatment. The oocytes were in vitro fertilized with 1.5×105/㎖ sperm concentration in four different mTBM medium not contained(control) and contained caffeine, MBCD or caffeine+MBCD for 6 hrs. After in vitro fertilization, embryos were transferred into PZM-3 with 0.03% BSA medium. The cleavage of embryo was evaluated at 48 and 96 hrs. Results showed that when the sperm was incubated in four different mTBM medium, the integrity of acrosome was significantly (p<0.05) lower treated with MBCD than other treatment groups at 0, 30 and 360min. The cleavage rates of pig embryos was significantly (p<0.05) lower in control than other treatment groups, However, It was not significantly different between groups. In conclusion, the MBCD treatment in pig sperm showed effect on acrosome reaction, but
cleavage rate of embryo was not affected.

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