• 한국수정란이식학회지
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• 제29권3호
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• pp.283-287
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• 2014

Sexed semen is commonly used for the production of calves of the desired gender. Gender selection is important in animal production industries. For example, female cattle are required for the dairy industry while males are preferred in the beef cattle industry. The present study was to assess the in vivo embryo production efficiency using the semen separated according to sex during superovulation in Hanwoo. Seventy Hanwoo donor cows were flushed on day 7 of estrus cycle with same FSH and artificial insemination by the same technicians. Embryos were recovered on 7 days after the third insemination by flushing the uterus with embryo collection medium. KPN semen straws used artificial insemination contained 20 million sperm (total number 60 million per donor). Sex-sorted semen straws contained 4 million sperm (total number 12 million per donor). The results obtained were as follows: No differences were observed in the efficiency of superovulation rates on KPN semen 87%, and sexed semen 100%, respectively. The mean numbers of total embryos are each $12.58{\pm}8.31$ and $13.25{\pm}7.86$. The mean numbers of transferable embryos, sexed semen were significantly lower than KPN semen ($3.75{\pm}1.98$ vs. $8.23{\pm}6.07$, P<0.05). The rates of unfertilized embryos from superovulation using sexed semen were significantly higher than KPN semen (50% vs. 15%, P<0.05). The rate of degenerated 2-cell embryos from sexed and KPN semen was 60.87% and 11.11%, respectively (p<0.05). In conclusion, these results indicate that superovulation using sexed semen was useful, but efficient embryo production was important to reducing the damage caused by the Flowcytometer-based sperm sorting procedure.

• Reproductive and Developmental Biology
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• 제29권4호
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• pp.229-234
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• 2005

Methods for activation of reconstructed oocytes were examined for the production of nuclear transfer (NT) rat embryos using fetal neural stem cells as donor. Neural stem cells were isolated from Day 14.5 rat fetuses, and the oocytes for recipient cytoplasm were recovered from 4-week old Sprague Dawley rats. After enucleation and nuclear injection, the reconstructed oocytes were immediately exposed to activation medium consisting of 10 mM $SrCl_2$ for 4 h (immediate activation after injection; IAI), or cultured in vitro for $2\~3$ h before activation treatment (injection before activation; IBA). Pre-activated oocytes were also used for NT to test reprogramming potential of artificially activated oocytes. The oocytes were grouped as IIA (immediate injection after activation) and ABI (activation $2\~3$ h before injection). Following NT, the oocytes were cultured in vitro. Development of the NT embryos was monitored at 44 and 119 h after activation. The embryos in groups IAI, mA, and IIA were cleaved to the 2-cell stage at the rates of $36.6\%\;(15/41),\;39.5\%\;(17/43)\;and\;46.3\%$ (25/54), respectively. However, in the ABI group, only one embryo ($1.8\%$, 1/55) was cleaved after activation. After in vitro culture, two NT embryos from IAI group had developed to the morula stage $(4.9\%\cdot2/41)$. However, no morula or blastocyst was obtained in the other groups. These results suggest that immediate activation after injection (IAI) method may be used for the production of rat somatic cell NT embryos.

• 한국수정란이식학회지
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• 제29권3호
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• pp.229-234
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• 2014

The aim of the present study was to compare two different serum-free media, modified synthetic oviduct fluid (mSOF) and modified potassium simplex optimization medium (mKSOM) containing 20% RD (RPMI1640 + DMEM, 1:1 v/v) (RD-mKSOM), for in vitro culture (IVC) of bovine embryos. After in vitro maturation and fertilization, the presumptive zygotes were cultured in two different serum-free conditions for 7 days and 9 days to evaluate blastocyst formation and hatching, respectively. Serum supplemented conventional CR2 medium was used as control. After 7 day of culture, there was no significant difference in cleavage and blastocyst formation rates among three groups (mSOF, 59.3 and 30.1%; RD-mKSOM, 65.0 and 41.5%; control, 51.6 and 38.0%, respectively). Hatching rate was significantly higher in control (69.0%) than other experimental groups (mSOF, 22.0%; RD-mKSOM, 39.5%) (P<0.0001 and P<0.001, respectively). Although both serum-free conditions showed lower hatching rates than serum-added control, in serum-free groups, RD-mKSOM showed significantly higher hatching rate than mSOF (P<0.001). In addition, one-step using RD-mKSOM may facilitate IVC procedure than two-step culture system. In conclusion, the results indicate that one-step RD-mKSOM is more suitable defined culture system for IVC of bovine embryos than two-step mSOF.

• 한국수정란이식학회지
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• 제28권1호
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• pp.31-39
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• 2013

Alpha-tocopherol as an antioxidant acts in preservation of chilled semen by preserving cell membrane damage from lipid peroxidation. Optimum concentrations of ${\alpha}$-tocopherol in egg yolk-citrate (EYC) extender need to be studied in crossbred bull's semen. Different concentrations of ${\alpha}$-tocopherol viz. 0, 1, 2, 4 and 6mg per ml of extender were used. Semen was collected once a week from four bulls used to regular collection, aged 4 to 7 years, weighing 320 to 450 kg, and with body condition score 4 to 4.5 and scrotal circumference 23 to 32 cm. Semen was evaluated routinely and sperm morphology was viewed under light microscope at ${\times}1,000$ magnification after fixing with buffered formal saline. Over 90% had normal head, acrosome, mid-piece and tail. Semen was diluted with egg-yolk-citrate extender to produce $15{\times}10^6$ spermatozoa/ml and 0, 1, 2, 4 and 6 mg/ml ${\alpha}$-tocopherol were added. The semens amples were kept at $8^{\circ}C$. Sperm motility and viability were examined daily up to 5 days under light microscopy at ${\times}200$ magnification. Sperm viability was acceptable (${\geq}40%$) up to the $4^{th}$ day with all concentrations of ${\alpha}$-tocopherol and up to the $5^{th}$ day with 2 mg/ml ${\alpha}$-tocopherol. Sperm motility was acceptable (${\geq}40%$) up to the $3^{rd}$ day irrespective of ${\alpha}$-tocopherol concentration, and up to the $4^{th}$ day with 2 mg/ml ${\alpha}$-tocopherol. It is suggested that the lifespan of chilled semen may be extended up to 4 days by adding 2mg/ml ${\alpha}$-tocopherol.

• 한국수정란이식학회:학술대회논문집
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• 한국수정란이식학회 2002년도 국제심포지엄
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• pp.34-36
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• 2002

Epidermal growth factor (EGF) and insulin-like growth factor-I (IGF-I) have been shown to stimulate proliferation and differentiation of various somatic cells, including placental trophoblasts and also to enhance fetal growth and development when maternally administered. Since an increase of the expression of placental EGF and IGF-I receptors in rat, mouse, and human with the gestation advanced, both EGF and IGF-I were considered to play pivotal roles on fetal growth by regulating some function of placental cells. Amino acids are crucial importance for both maternal and fetal requirements of energy source and essential constituent of fetal mass during pregnancy. Impaired fetal and placental uptake of amino acids has been observed in several models of growth retardation in the rat. Amino acid is concentrated in the fetal side through active transport by amino acid transporters and is one of the important metabolic fuels for the fatal growth. Therefore, at first plasma amino acid concentrations in mothers and fetuses were measured as an index of uphill transport across the placenta associated with EGF and IGF-1. The EGF administration at the concentration of 0, 0.1, or 0.2 $\mu\textrm{g}$/g to pregnant rats from day 18 to 21 of gestation apparently increased fetal/maternal ratio of serum proline concentration and also fatal growth in EGF dose-dependent manner. When IGF-I in doses of 0, 1, 2, and 4 $\mu\textrm{g}$/g were administrated, the ratio of leucine, isoleucine, tryptophan, phenylalanine, tyrosine and also fetal growth significantly increased with a dose-dependent manner. These results suggested that EGF and IGF-I enhanced fatal growth by, as one of its possible mechanisms, promoting placental activity to transfer some amino acid supplies from the mother to the fetus in late pregnancy.

• 한국수정란이식학회지
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• 제21권4호
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• pp.299-306
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• 2006

본 연구는 수정란이식의 현장 적용 측면을 중심으로, 한우 체외 수정란의 발생 단계, 일자 및 등급이 젖소 대리모에 이식 후 임신과 유산, 분만과 관련된 임신기간, 생시체중, 난산 및 쌍자율을 조사하였다. 또한 단자 및 쌍자 분만에 따른 임신기간, 생시체중, 성비 및 폐사율을 분석하였다. 발생 단계에 따른 임신율은 배반포 단계(64.4%), 유산율은 부화 배반포(HB) 단계(21.4%)가 유의하게 높았다(p<0.05). 발생 일령에 따른 임신율은 7일령 배가 49.0%로서 8일 및 9일령의 36.4 및 15.4%보다 유의하게 높았으나(p<0.05), 유산율은 0$\sim$10.7%로 비슷한 경향이었다. 등급에 따른 임신율은 41.4$\sim$42.5%, 유산율은 9.3$\sim$16.5%로서 차이가 없었다. 발생 단계에 따른 임신기간, 송아지의 체중 및 난산율은 비슷한 경향이었으나, 쌍자율은 HB 단계가 44%로서 배반포 단계의 15.8%보다 유의하게 높았다(p<0.05). 발생 일령에 따른 임신 기간, 난산율 및 쌍자율은 차이가 없었으나, 송아지의 체중은 9일령의 것이 평균 35.5 kg으로서 7일령 및 8일령의 평균 25.2 및 26.2kg보다 유의하게 무거웠다(p<0.05). 등급에 따른 임신 기간은 1등 및 2등급이 평균 278.5 및 276.1일로서 3등급의 평균 273.7일에 비하여 유의하게 길었으나(p<0.05), 체중, 난산율 및 쌍자율은 차이가 없었다. 분만한 송아지의 개체 수에 따른 임신기간은 단자가 평균 278.5일로서 쌍자의 평균 272.5일보다 유의하게 길었다(p<0.05). 생시 체중도 단자가 평균 29.6 kg으로서 쌍자의 평균 22.3kg에 비하여 유의하게 무거웠으나(p<0.05), 성비와 폐사율은 유사한 경향이었다.

• 한국수정란이식학회지
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• 제27권1호
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• pp.51-55
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• 2012

The objective of this study was to investigate the motility and kinematics of boar sperm that while stored at 4C. The samples of fresh boar semen were place into an extender, Androhep, and stored at $4^{\circ}C$. In three of these samples, cryoprotectants were added. The sperm's motilities and kinematics were evaluated by using microscope (${\times}400$) and the viability status was evaluated by using with eosin staining method. The 5 sample groups are; Goup A:Androhep (extender), stored at $17^{\circ}C$. Group B:Androhep (extender), stored at $4^{\circ}C$. Group C:Androhep (extender), + 3% glycerol (cryoprotectant), stored at $4^{\circ}C$. Group D:Androhep (extender), + 3% DMSO (cryoprotectant), stored at $4^{\circ}C$. Group E:Androhep (extender), + 3% ethylene glycol (cryoprotectant), stored at $4^{\circ}C$. In group A, the sperm's motility was reduced. On day one the sperm's motility was ($85.7{\pm}2.3$) and day 5 the motility was ($43.9{\pm}3.3$). In group B, C and D the sperm's motility were reduced to 0 on day 5. In group E the sperm's percentage of motility decreased. On day one the sperm's motility was ($42.0{\pm}0.5$) and day 5 the motility was ($2.3{\pm}0.3$). When comparing cryoprotectant in samples of boar sperm there is a slight improvement in the results when the use of Androhep Lite (extender), + 3% ethylene glycol (cryoprotectant), stored at $4^{\circ}C$ are used. Based on these results, ethylene glycol can protect sperm from heat shock at $4^{\circ}C$, but not satisfactory level. However, it showed the possibilities of liquid semen preservation at $4^{\circ}C$ by using cryoprotectant.

• 한국수정란이식학회지
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• 제18권3호
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• pp.257-262
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• 2003

종빈돈의 번식효율 증진을 위해 후보종빈돈의 분만후 포유기간, 등지방두께 등이 번식능력에 영향을 미치는 요인을 조사ㆍ분석하여 우수한 후보 종빈돈의 조기선발에 활용코자 수행한 결과는 다음과 같다. 1. 분만모돈의 포유기간이 17∼21일일 때에 등지방두께는 19.19mm였고, 포유기간이 22∼26일 일때에는 16.52mm로 포유기간이 길수록 분만모돈의 이유시 등지방두께는 유의적으로 얇았다.(p<0.01). 2. 분만모돈의 포유기간이 17∼21일인 경우에 발정재귀일은 5.76일, 22∼26일인 경우 5.62일로 포유기간에 따른 차이는 없었다. 3. 분만모돈의 이유후 등지방두께가 13∼16mm인 경우에 발정재귀일은 5.69일, 17∼20mm인 경우 5.67일, 21∼23mm인 경우 5.75일로 이유후 등지방 두께는 발정재귀일에 크게 영향을 미치지 않았다. 4. 혈중 estradiol 의 농도는 분만시 28.49pg/$m\ell$, 이유시 12.29pg/$m\ell$, 발정재귀시 16.52pg/$m\ell$ 이었으며, 혈중 progesterone의 농도는 분만시 1.50 ng/$m\ell$, 이유시 0.69 ng/$m\ell$, 발정재귀시 0.94ng/$m\ell$ 수준이었고, 혈중 cortisol 의 농도는 분만시 57.74ng/$m\ell$, 이유시 43.01ng/$m\ell$, 발정재귀시 47.89ng/$m\ell$이었으며, estradiol, progesterone 및 cortisol 의 혈중농도는 분만시가 가장 높은 수준으로 나타났다.

• 한국수정란이식학회지
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• 제18권3호
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• pp.187-193
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• 2003

본 연구는 한우에 GnRH ＋ PGF$_2$$\alpha$＋GnRH (Ov-synch)를 처리하여 배란동기화를 시켰으며, 2차 GnRH 투여후 배란시간, 수태율, 계절별 수태율, 산차별 수태율을 조사하였으며, 시험축은 2산 이상의 개체를 무작위로 선발하여 실험에 공시하였으며, 배란동기화 처리후 1회 인공수정을 실시하고 수태율을 환산하였다. 호르몬 처리방법으로는 GnRH ＋ PGF$_2$$\alpha$ ＋ Gn-RH(Ov-synch)법을 이용하였으며, 배란시간의 조사는 초음파를 이용하여 2차 GnRH 투여 후 24시간부터 31시간까지 2시간 간격으로 난소를 촬영하여 배란 여부를 조사하였다. 1. 배란동기화 처리후 24시간부터 31시간까지 2시간 간격으로 난소의 상태를 확인한 결과 28∼30시간 사이에 80%(20/25)로 가장 많이 배란된 것으로 나타났다. 2. 수태율에 있어서는 계통별 1회 수정 수태율은 고급육 계통이 48.1%(38/79)로 다소 높게 나타났다. 3. 산차에 따른 수태율은 1∼2, 3∼4산차에서 각각 44.3, 55%로 나타났다. 4. 계절별로는 여름보다는 봄과 가을에서 47.3%로 다소 높은 경향이였다.

• 한국수정란이식학회지
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• 제19권3호
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• pp.257-264
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• 2004

멸종위험이 큰 우리나라 재래돼지를 유전자원으로서 안전하게 보존하고 유전적 다양성을 유지하기 위한 수단으로 수정란을 채취하여 동결보존하기 위해서 미경산 재래돼지에서 과배란 유기를 위한 적정 호르몬의 수준과 수정란의 회수 및 동결보존 방법을 확립하고자 수행한 결과는 다음과 같다. 1. hCG 500IU와 PMSG를 500, 750, 1,000IU 및 hCG 750IU와 PMSG 1,000IU를 각각 투여한 재래돼지의 배란황체와 미배란난포의 수는 각각 12.4, 13.6, 30.0 및 23.3개로 PMSG 1,000IU와 hCG 500IU를 투여한 재래돼지가 다른 용량의 처리돼지보다 난소반응이 양호하였으나 유의적인 차이는 없었으며, 배란황체수에 대한 수정란 회수율은 59.4-79.2％ 수준이었다. 2. 과배란처리된 공란돈에서 수정후 4일에 회수된 수정란의 발육단계는 상실기의 수정란이 수정후 5일보다 유의적으로 많이 회수되었으며(P<0.01), 수정후 5일에 회수된 배 반포기의 수정란을 수정후 4일보다 유의적으로 많이 회수되었다(P<0.05). 3. 확장배반포기 수정란을 1.4M glycerol의 항동 해제를 이용하여 관행의 완만동결법으로 동결한 처리에서 생존율은 25.3％였다.