본 연구는 농산부산물을 이용한 발효사료의 급여효과를 알아보기 위해 비육 흑염소의 생산성 및 영양소 이용률을 조사하였다. 증체조사를 위한 사양시험은 거세흑염소 24두를 이용하여 처리구당 6두씩 30일 수행하였고, 소화율시험은 거세흑염소 12두를 공시하여 처리구당3두씩 라틴방각법으로 실시하여, 처리구는 대조구(배합사료 및 볏짚 급여구)와 3개의 시험구(발효사료와 볏짚 급여구)로 각각 배치하였다. 일당증체량은 대조구가 가장 높았고, T3구가 가장 낮았다(p<0.05). 1일 두당 건물섭취량 과 유기물섭취량은 시판사료를 급여한 대조구가 각각 718.8과 680.9 g, 농산부산물 첨가구가각각 634.2~699.2와 602.8~660.4 g으로 나타나농산부산물 중 미강 첨가구가 높을수록 섭취량이 낮아지는 경향으로 나타났다. 건물과 유기물 소화율은 대조구가 농산부산물 첨가구보다유의하게 높았고(p<0.05). 시험구간에는 미강을30% 첨가한 T3구가 가장 낮았다(p<0.05). 질소축적률은 대조구와 T1구가 유의하게 높았다.따라서, 본 연구의 결과 농산부산물을 이용한발효사료(T1과 T2구)는 시판사료를 급여한 대조구와 비교 시 증체는 86~90%, 건물소화율은91.7~93.1%의 수준을 보였으며, 질소이용성은대등한 수준을 보였다. 그러나 미강의 첨가 비율이 높아질수록 사료효율 저하가 우려되므로조지방 함량을 5.0% 이하로 배합하는 것이 필요하다 판단된다.

We investigated the effect of glutathione supplementation on body weight gain, feed intake, velvet antler yield and economic analysis in elk bulls. A total 14, 2-year old male elks were divided into 2 groups with control or glutathione treatment. Elks were fed concentrate feed at the level of 1.5% relative to body weight (3.1 kg). and allowed to consumed hay as roughage ad libitum. Glutathione was supplemented at the level of 6 mg/kg. Average daily gains (ADG) for 2-years old elks were 234.1± 7 and 247.6±22 kg in control and glutathione fed groups, respectively. Treated group had higher ADG than control (p<0.05). Individual daily DM intakes were 5.34±0.70 and 5.64±0.71 kg in control and glutathione supplemented groups, respectively. Glutathione-fed group showed an additional intake of 298 g on an average. Production of velvet antlers for elk yearlings was 4,229±720 g and 4,653±960 g in control and glutathione supplemented groups respectively. Analysis of economics efficiency revealed 8% higher revenue index in glutathione supplemented groups. In conclusion, glutathione supplementation showed increase of DM intake and ADG in elk bulls, and could also increase velvet antler production.

Previously, we reported that the osmolarity conditions in the satellite region were affected CpG DNA methylation status while Pre-1 sequence was not affected CpG DNA methylation in pNT blastocyst stage. This study was conducted to investigate the DNA methylation status of repeat sequences in pig nuclear transfer (pNT) embryos produced under different osmolarity culture conditions. Control group of pNT embryos was cultured in PZM-3 for six days. Other two treatment groups of pNT embryos were cultured in modified PZM-3 with 138 mM NaCl or 0.05 M sucrose (mPZM-3, 320 mOsmol) for two days, and then cultured in PZM-3 (270 mOsmol) for four days. The DNA methylation status of the Pre-1 sequences in blastocysts was characterized using a bisulfite-sequencing method. Intriguingly, in the present study, we found the unique DNA methylation at several non-CpG sequences at the Pre-1 sequences in all groups. The non-CpG methylation was hypermethylated in all three groups, including in vivo group (86.90% of PZM- 3; 83.87% of NaCl; 84.82% of sucrose; 90.94% of in vivo embryos). To determine whether certain non-CpG methylated sites were preferentially methylated, we also investigated the methylation degree of CpA, CpT and CpC. Excepting in vivo group, preference of methylation was CpT>CpC>CpA in all three groups investigated. These results indicate that DNA methylation of Pre-1 sequences was hypermethylated in CpG as well as non-CpG site, regardless modification of osmolarity in a culture media.

We investigated the effect of glutathione supplementation on feed intake, body weight gain, velvet antler yields and economics of elk yearling. Fourteen elk yearlings were divided into 2 groups. Seven yearlings in each group (control and treatment) were fed with 1.5-2.5 percent body weight (%BW) of concentrate feed for elk, voluntary intake of hay as roughage and 6 mg/kg body weight (KBW) of glutathione. The results were as follows. Average daily gain (ADG) for control elk yearlings for first 1.5 month was 0.46 kg, while that of glutathione supplemented was 0.55 kg. Although glutathione fed group had higher ADG compared to control group (p<0.05), ADG after 1.5 month showed no difference. In spring, daily DM intake per elk yearlings was 3.98 and 4.24 kg for control and glutathione supplemented groups, respectively. The statistical differences in feed intake between two groups were not observed. However, feed intake tends to increase in glutathione fed group. Production of velvet antlers for elk yearlings were 911±256 and 1066±357 g for control and glutathione supplemented groups, respectively. Statistical difference between two groups was not observed due to the high variation. In economic analysis, additional 109,110 KRW per head for the cost of glutathione resulted in 2 percent higher revenue index due to the increased antler production. In conclusion, feeding glutathione to elk deers effectively increased DM intake and ADG of elk yearlings. Glutathione supplementation in feed might increase velvet antler production as well as ADG.

This study was conducted to investigate the survival rate of frozen-thawed spermatozoa in equine by glycerol concentration and freezing speed. Two stallions (1 Thoroughbred-13 year old and 1 Arab-7 year old) bred in Korea Racing authority was examined for 1 times in a couple of weeks. Semen was collected by condom method standing heated mare and were centrifuged 650 g for 15 min. and isolated the seminal plasma. Thick fraction of semen was diluted EDTA-Lactose-egg yolk diluents to 1:1 and contained in 0.5 ml straw as 6～14×107cells/ml. Final concentrations of glycerol were 3, 5 and 7% in cryopreseved diluents and added 4 times for 2 hours equilibration. For the freezing, equilibrated straws were located 3 or 5 cm above LN2 gas for 5 or 10 min. Survival rates of pre-frozen sperm were 65.0±13.2%, 68.3±10.4%, 66.7±11.5% and post-frozen were 53.3±23.1%, 45.0±15.0%, 50.0±18.0% in 3, 5, 7% glycerol concentration, respectively. There was no difference between glycerol concentrations. Survival rates of frozen-thawed sperm on freezing speed were 36.7±10.4%, 40.0±7.1%, 30.0±13.2% at 3 cm－5 min and 33.3±11.5%, 31.7± 2.9%, 21.7±10.4% at 3 cm－10 min in 3, 5, 7% glycerol concentration, respectively. Survival rates of frozen-thawed sperm on freezing speed were 43.3±15.3%, 32.0±17.9%, 22.3±15.7% at 5cm－5 min and were 47.5±15.0%, 43.3±12.6%, 48.3±15.3% at 5cm－10 min in 3, 5, 7% glycerol concentration, respectively. There were significantly different between groups (p<0.05). These results suggest that glycerol concentration did not affect cryopreservation of stallion semen within 3～7% but freezing speed affects. In our experiment, the best cryopreservation condition was at 5 cm above LN2 gas for 10 min for pre-freezing and 7% of glycerol concentration. These results lead to commercial AI with frozen-thawed stallion semen.

The objective of this study was investigate the superovulation treatment and to relate concentrations of blood urea nitrogen(BUN) in Hanwoo donors. Thirty six, at random stages of the estrous cycle, received a CIDR. Four days later, the animals were superovulated with a total of 28AU FSH (Antorin, 2AU=1 ml) administered twice daily in constant doses over 4 days. On the 3th administration of FSH, CIDR was withdrawn and 25 mg PGF2α was administered. Cows were artificially inseminated twice after estrous detection at 12 hr intervals. The cows received 100 μg GnRH at the time of 1st insemination. Embryos were recovered 7 or 8 days after the 1st insemination. Cows with BUN ＜10, 11～18 and ≥19 mg/dl had return of estrus of 34.6, 30.5 and 30.4 days respectively. Return of estrus after superovulation treatment was not significantly lower for cows with blood urea nitrogen (BUN) above 10 mg/dl than for cows with BUN below 10 mg/dl. Cows with BUN ＜10, 11～18 and ≥19 mg/dl had number of transferable embryos of 3.2±1.2, 5.4±1.9 and 4.1±2.1 respectively.

Osmolarity of culture media is one of the most important factors affecting in vitro development. This study was conducted to investigate the DNA methylation status of Pre-1 and satellite sequence in pig nuclear transfer (pNT) embryos produced under different osmolarity culture conditions. Control group of pNT embryos was cultured in PZM-3 for six days. Other two treatment groups of pNT embryos were cultured in modified PZM-3 with 138 mM NaCl or 0.05M sucrose (mPZM-3, 320 mOsmol) for two days, and then cultured in PZM-3 (270 mOsmol) for four days. Previous our studies have reported that pNT embryos cultured in both hypertonic media showed significantly higher blastocyst formation rate than that of control. The DNA methylation status of the satellite sequences in blastocyst was characterized using bisulfite-sequencing technology. The satellite region had a similar methylation pattern of in vivo blastocyst among two culture groups excepting the control group. Each level of methylation is that the satellite DNA moderately methylated (43.10% of PZM-3; 56.12% of NaCl; 55.06% of sucrose; 60.00% of in vivo embryos). As a result of the sequence of PRE-1, CpG methylation pattern was similar to three groups, including in vivo group. In case of the satellite DNA region, the osmolarity conditions were affected CpG DNA methylation status while PRE-1 sequence was not affected CpG DNA methylation in pNT blastocyst stage. These results indicate that the modification of osmolarity in a culture media may influence to spatially change of DNA methylation of repetitive sequence for pNT embryo development.

그래픽스 렌더링 파이프라인 (응용, 기하, 레스터화)은 컴퓨터 게임에서 가장 중요한 기능인 실시간 그래픽스 렌더링의 핵심이다. 일반적으로 그래픽스 렌더링은 CPU와 GPU의 두 장치의 협조에 의해 완성되며 이 협조 과정에서 병목이 발생할 수 있다. 본 논문에서는 CPU와 GPV 사이에 발생하는 병목현상을 줄이는 데 초점을 맞추어, 보통은 하나의 스레드로 처리되는 CPU 연산을 순수 CPU 연산과 GPV와 연관된 연산의 두 가지로 구분하여 서로 독립적인 스레드로 병렬처리 되게 함으로써 실시간 그래픽스 렌더링의 성능을 향상시키는 방법을 제안한다. 이 방법은 CPU와 GPV사이의 협조를 위한 전송 과정에서의 병렬성을 극대화한다. 실험을 통하여 제안하는 방법이 기존의 방법 보다 더 빠르게 그래픽스 렌더링을 수행함을 검증하였다. 또한 본 논문에서는 CPU와 GPU의 협조 과정에서 생기는 병목현상으로 인한 유휴시간을 잘 활용하여 렌더링 파이프라인의 균형을 맞추면서 렌더링의 질을 높이는 방법도 제안한다. 제안하는 방법들을 우리가 개발한 네트워크 게임 엔진에 적용하여 실제 시스템에서도 효과가 있음을 확인하였다.