In the present study, we investigated the effects of genotypes on in vitro maturation and fertilization in porcine fresh/frozen-thawed oocytes. The porcine cumulus-oocyte complexes (COCs) were divided into four groups according to whether they were: (1) in vitro matured; (2) cryopreserved and in vitro matured; (3) in vitro fertilized and (4) cryopreserved, and in vitro fertilized. Maturation of porcine COCs was accomplished by incubation in NCSU23 medium. Immature oocytes were cryopreserved by Open Pulled Straws (OPS) method according to Vajta et al., (1998). Oocytes stained by Acetic-Orcein method were observed under the microscope. DNA extracted from the ovaries was analyzed by RAPD (random amplified polymorphic DNA) and SSCP (single strand conformational polymorphisrrt) method. The rates of oocytes maturation and fertilization were significantly high in AA genotype. The results indicated that in vitro maturation and fertilization in porcine fresh/frozen-thawed oocytes may be affected by genotypes in pigs.

본 연구는 New Zealand White 수토끼에서 춘기발동 기간 동안에 혈청내 IGF-I(insulin-like growth factor-I)과 GH(growth hormone) 수준의 변화, 정자 형성에 따른 정소내 세포 구성 변화 및 이들 측정치들 간에 관계를 조사하기 위하여 실시되었다. 주령과 관련된 정소내 세포의 DNA 함량 변화 조사를 위하여 10~28주령 수토끼 정소 조직의 fine-needle biopsy를 flow cytometry(FCM)로 분석하였다. 생체중은 12~20주령 때 크게 증가되었고(P<0.05), 28주령 체중은 3.4kg이었다. 혈청 IGF-I 수준(451.3ng/mL)은 20주령에서 가장 높았으며(P<0.05), 그 후 낮은 수준으로 유지되었다. 혈청 GH 수준은 183.3pg/mL으로 다른 주령 때보다 현저히 높았으며(P<0.05), 상승시기가 IGF-I보다는 다소 빨랐다. 정소 조직세포 중 1C-세포의 상대적 비율은 18주령 때 48.2%로 16주령보다 크게 상승되었고(P<0.05), 주령 증가와 더불어 68%로 증가되었다. 2C-세포 비율은 18주령 때 26.8%로 16주령의 54.3%보다 현저히 낮았다(P<0.05). 4C-세포 비율은 18주령 때 9.9%를 제외하고 2~6%를 유지하였다. 이상 결과에서 토끼는 춘기 발동 개시가 약 18주령에 일어나고 이 기간 중 IGF-I과 GH 수준의 변화가 나이 또는 체성장과 관계가 있었으며 그 영향이 정자 형성과 관련이 있음을 알 수 있었다. Fine-needle biopsy와 연계된 FCM은 춘기 발동 개시와 관련된 정자의 형성 과정을 평가하는데 매우 정확한 방법임을 확인할 수 있었다.

This study was carried out to evaluate the effects of glucose and sodium phosphate on in vitro development of porcine oocytes matured and fertilized in vitro. When the culture medium was supplemented with various concentrations of glucose, the higher proportions (23 and 26%) of oocytes developed to morular or blastocyst stages were at the concentrations of 2.78 and 5.56 mM than 0 (9%; P<0.05) and 11.12 mM (18%). In experiment to evaluate effect of sodium phosphate during in vitro development of porcine oocytes, a significantly (P<0.05) higher proportions of embryos developed to morular or blastocyst stages was obtained with sodium phosphateof 0.28 (25%) and 0.53 (27％) mM than 0 (15%), 1.05 (19%) and 2.10 (10%) mM. On the other hand, when oocytes were cultured in medium with (0.53 mM) sodium phosphate, the proportions of developed embryos were significantly (P<0.05) higher in medium without (29%) that than with (14%) 5.56 mM glucose. However, a higher proportion of embryos developed to morular or blastocyst stages were obtained in medium with (23%) that than without (8%) glucose (P<0.05). The minimum essential medium (MEM) added to the culture medium were higher regardless of presence of sodium phosphate and glucose on the development of embryos. Although sodium phosphate and glucose could support morular and blastocyst development to a limited extend (10∼24%), significantly higher proportion (36%) at morular or blastocyst stages was obtained by MEM adding in the medium with sodium phosphate and glucose. These results suggest that the early development of in vitro fertilized porcine oocytes can be maintained efficiently by glucose and sodium phosphate when they were cultured in medium with MEM.

This study was carried out to investigate the effect of cysteamine addition during in vitro maturation, fertilization and culture of porcine oocytes. Oocytes were matured for the first 22 h in mTCM -199 media supplemented with or without 150 μM cysteamine. They then were matured for an additional 22 h in mTCM-199 media without hormones supplemented with or without 150 μM cysteamine. When cumulus-oocyte complexes (COCs) were matured in the mTCM-199 media supplemented with cysteamine, the rates of GVBD and maturation (metaphase Ⅱ) were enhanced as compared to the media without the addition of cysteamine. Also, when COCs were matured in the mTCM-199 media supplemented with cysteamine, the rates of sperm penetration, male pronucleus formation, cleavage and blastocyst formation after in vitro fertilization were enhanced as compared to the media without the addition of cysteamine. In conclusion, it was suggested that oocytes matured for the first 22 h in mTCM-199 media supplemented with 150 μM cysteamine increased the rates of metaphase Ⅱ, sperm penetration, male pronucleus and blastocyst formation were higher as compared to the media without addition of cysteamine.