본 연구에서는 한우 암소와 씨수소의 육종가를 기반으로 연도별 유전적 개량량을 추정하여 현재 한우 축군의 개량 정도를 파악하여 향후 한우 개량 방향을 위한 기초자료로 활용하고자 본 연구를 시행하였다. 본 연구를 위하여 한우농가 4,040호에서 축산물품질평가원에 도축된 970,567두의 도축자료를 이용하여 10번 반복되어 추출된 표본 자료와 한우농가에서 2009년부터 2019년까지 사육되고 도축된 개체 중에서 한국종축개량협회에 혈통등록 되어 있는 거세우를 선별하여 결측치 및 이상치를 제거하고 도축월령이 27~32개월 이외의 기록은 분석에서 제외한 후, 1,391,141두의 도체 자료를 분석에 이용하였다. 이용된 형질은 도체중(Carcass Weight, CW), 등심단면적(Eye Muscle Area, EMA), 등지방두께(Backfat Thickness, BF) 및 근내지방도(Marbling Score, MS)의 4개 형질을 고려하였다. Random Sampling 10 반복되어 추출된 Data 1의 도체중, 등심단면적, 등지방두께 및 근내지방도의 개량추세에 대한 회귀계수는 매년 평균 0.44㎏, 0.197㎠, -0.051㎜ 및 0.034점으로 나타났으며, 도축성적을 보유한 전체 개체의 자료로 구성된 Data 2에서는 각각 0.35㎏, 0.22㎠, 0.06㎜ 및 0.04점의 개량추세를 보였다. Data 2에서 씨수소의 개량추세는 1.54㎏, 0.343㎠, -0.045㎜ 및 0.050점의 추세를 보였으며 암소와 씨수소 간에는 1.19㎏, 0.119㎠, -0.014㎜ 및 0.010점의 차이를 보였다. 유전적 개량량을 확인하기 위하여 육종가의 표준편차를 이용하였으며, 암소의 선발강도는 본 연구에서 보고한 암소의 후대 거세우 기록 빈도 및 비율을 통해 계산하였다. 한우 암소의 선발 시기를 3산차 이전을 기준으로 하는 것과 4산차 이후를 기준으로 하는 것으로 나눠서 선발강도를 적용하였다. 그 결과, 암소의 선발 시기를 3산차 이전으로 했을 때 세대당 유전적 개량량은 도체중, 등심단면적, 등지방두께 및 근내지방도에서 각각 5.04㎏, 1.31㎠, 0.71㎜ 및 0.32점으로 나타났다. 이러한 결과를 바탕으로 현재 한우 암소집단에서 정확한 육종가를 추정하고, 유전적 개량량을 높이기 위해서는 후대의 기록을 높이기 위한 육종 계획이 필요할 것으로 판단된다.

In the present study, we examined the effect of straw size on spermatozoa motility, viability, acrosome integrity, mitochondrial membrane potential, and plasma membrane integrity after freezing-thawing. Hanwoo semen was collected from three bulls and diluted with an animal protein-free extender, divided into two groups, namely, 10 million spermatozoa in 0.25 mL and 20 million spermatozoa in 0.5 mL straw, and cryopreserved. In Experiment 1, the motility and motility parameters of the frozenthawed spermatozoa were evaluated. After freezing-thawing, the spermatozoa motility parameters fast progressive, straight line velocity, and average path velocity were compared between the 0.25 mL straw and 0.5 mL straw groups. They were 35.2 ± 1.0 and 32.3 ± 0.7%, 34.6 ± 0.7 and 31.8 ± 0.5 μm/s, 51.4 ± 1.3 and 47.1 ± 1.1 μm/s, 0.25 mL straw and 0.5 mL straw groups, respectively. In Experiment 2, the viability, acrosome membrane integrity, and mitochondrial membrane potential of the frozen-thawed spermatozoa were assessed. After freezing-thawing, the percentages of spermatozoa with live, intact acrosomes and high mitochondrial membrane potential were compared between the in 0.25 mL straw and 0.5 mL straw groups. They were 48.0 ± 2.6% and 35.6 ± 2.8% between the 0.25 mL straw and 0.5 mL straw groups. In Experiment 3, the plasma membrane integrity of frozen-thawed spermatozoa was compared. After freezingthawing, the plasma membrane integrity was higher for the in 0.25 mL straw group than the 0.5 mL straw group. They were 62.0 ± 2.2 and 54.1 ± 1.3% between the 0.25 mL straw and 0.5 mL straw groups. In conclusion, our results suggest that freezing semen in 0.25 mL straw improves the relative motility, viability, and acrosomal, mitochondrial membrane potential, and plasma membrane integrity of Hanwoo bull spermatozoa.

본 연구는 티모시 건초와 농후 사료 위주의 사료를 급여한 한우 씨수소 정소상체 정자 체외수정 효율 조사를 통해 정자의 활용 가능성을 조사하였다. 농후 사료는 체중의 1.8%를 급여하고 양질의 티모시 건초를 자유채식 시킨 14개월령 거세우의 정소에서 분리된 정소상체 미부의 정자를 회수하고 동결 흉해 후 체외수정을 실시한 결과는 다음과 같다. 웅성전핵과 자성전핵이 형성(2PN)된 난자는 정상수정으로, 1개의 전핵(1PN), Expanded Sperm Head (ESH), Polyspermy 형태는 비정상적인 수정의 형태로 평가하였다. 정상적으로 수정된 난자의 비율은 정소상체 정자의 경우 전체 침투율은 49.7% 그리고 정상적인 2PN을 가진 난자는 18.5%를 보였으며, 대조구 정자의 전체 침투율은 54.4%로서 정소상체 정자 보다 높은 결과를 보였으나 유의적인 차이를 보이지는 않았다. 정상적으로 2PN을 형성한 비율은 36.7%로서 정소상체 정자를 이용한 정자 보다 높았으나 유의적인 차이는 없었다. 체외수정 후 발달률 조사에서 정소 상체 정자의 분할률은 81.2%, 대조구 정자는 82.7%로 유사한 결과를 보였으나, 배반포 발달률은 정소상체 정자 24.4%와 대조구 정자 12.2%로 정소상체 정자를 사용한 난자의 발달에서는 유의적으로 높았다(p<0.05).

In this study, we examined number, motility and plasma membrane integrity of spermatozoa from six regions of epididymis in bull. Six testicles with epididymides were castrated from six bulls (mean±standard error, age of days = 441.3±9.6, body weight (kg) = 367±8.4, scrotal circumference (cm) = 30.7±0.4) at Hanwoo Research Institute, NIAS and transported to laboratory within 1 hour. Testicular weight, length, width and circumference were recorded. Epididymis in each bull was randomly used for recovery of spermatozoa. Epididymis was divided into six regions: efferent duct (ED), caput, corpus, proximal cauda (Pcauda), distal cauda (Dcauda) and vas deferens (VD). In experiment 1, we examined sperm number of each region of epididymis. Each region of epididymis contained different number of spermatozoa: ED (37.8±15.7 × 106cells/ml, 8.2%), caput (93.6±18.8 × 106cells/ml, 20.2%), corpus (33.0±8.5 × 106cells/ml, 7.1%), Pcauda (104.2±23.5 × 106cells/ml, 22.5%), Dcauda (180.5±32.5 × 106cells/ml, 39.0%) and VD (14.0±5.0 × 106cells/ml, 3.0%). In experiment 2, sperm motility of each epididymal region was examined by computer assisted sperm analysis (SCA, MicroOptic) system. Sperm motility was divided into 4 groups (fast progressive, slow progressive, non-progressive and immotile) based on WHO guideline. Percentages of fast progressive of Pcauda and Dcauda (11.0±2.3 and 15.4±3.6%) were significantly higher than that of ED, Caput, Corpus and VD which is 0.1±0.1, 1.5±0.6, 1.9±0.7 and 0.3±0.2%, respectively (p<0.05). In experiment 3, percentage of intact plasma membrane spermatozoa of each regions were examined by hypoosmotic swelling test. Percentages of intact plasma spermatozoa were not significantly different among six regions of epididymis: ED, caput, corpus, Pcauda, Dcauda and VD which is 68.0±8.6, 74.0±5.3, 68.5±6.2, 70.8±5.5, 71.0±5.8 and 64.6±10.8%, respectively. In conclusion, in the present study, we found out distribution, motility and plasma membrane integrity of spermatozoa from six regions of epididymis in Hanwoo bull. These results will be contributed to basic research about spermatozoa transportation and characters in epididymis of bull.

The study aims to assess viability, acrosomal menbrane, integrity and mitochondria membrane potential of sperm separated using a percoll density gradient(45% and 90%) and swim-up methods using Hanwoo epididymal sperm frozen semen. Briefy, motile sperm separated using a percoll gradient and swim-up. 25 μl of sperm dilution from droplets were transferred to 1.5 mL tube and incubated with fluorescent probes at 39°C in dark as follows. After incubation, 75 μl of 5,5',6,6'-tetrachloro-1,1',3,3'- -JC-1; Mitochondrial Membrane Potential Detection kit, Cell Technology Inc., USA) working solution was mixed with sperm dilution and incubated for 30 min. One μl of Hoechst 33342 (H1339; Molecular Probe, Eugene, OR, USA) stock solution was mixed with sperm dilution and incubated for 10 min. And then, 0.5 μl of propidium iodide (PI) stock solution and 0.5 μl of fluorescein peanut agglutinin FITC conjugate (FITC-PNA; Vector Laboratories, FL-1071) were mixed with sperm dilution and incubated for 8 min. After mixing with fluorescent probes and sperm dilution, 5 μl of stained sperm dilution was mounted on a slide glass and covered with cover glass. More than 200 sperms in a slide glass were counted with × 400 magnification by fluorescent microscope (Eclipse Ci_L, Nikon, JAPAN) and evaluated viability, acrosomal membrane integrity, and mitochondrial membrane potential of sperm with triple band filter (DAPI/FITC/TRITC; Nikon, Tokyo, Japan). Live sperm were stained with Hoechst 33342(blue) and dead sperm were stained with PI (red). Damaged acrosomal membrane of sperm was stained with FITC-PNA (green) and intact acrosomal membrane of sperm was not stained. Both of sperm swim-up method with or without BSA separated to Live intact mitochondria (15.39±4.31 vs, 12.58±3.74, and) without significant difference. and percoll density gradient method also similar (7.29±6.54), swim-up method of sperm preparation appeared to be more efficacious in percentage recovery of motile sperm concentration compared to Density gradient method.

Sperm recovery from epididymis in animals considered as important tools to preserve high-value or endangered species. However, there are no appropriate castrating indicators of timing for recovery of sperm which can be available to artificial reproduction technologies such as artificial insemination (AI) and in vitro fertilization (IVF), particularly in young Hanwoo bull. Therefore, this study aimed to investigate semen volume, morphology and motility of sperm in epididymis of young Hanwoo bulls at 8, 13, 14, and 15 months of age. About 2 cm of the epididymal tail only was cut and minced using blades. Minced epididymal tail tissues were mixed with semen extender (OptixCell, France, IMV technologies) and sperm were recovered with a cell strainer (100 μm nylon mesh). The number of sperm at 8 months of age was lower than that at 13, 14, 15 months of age in bulls after collection (33.6±27.2 vs. 352.4±39.2, 320.4±113.6 and 422.8±252.4×107cells respectively; P<0.05). After the frozen-thawed sperm the the percentage of abnormal head, tail and dead damaged acrosome did not differ between the ages 13, 14 and 15 months of age in bulls (P>0.05), however, the dead sperm with intact acrosome (DIA), the numbers showed that more than 15 months in 8, 13, 14 months (8.7±4.1 vs. 47.3±12.2, 34.8±14.0, 28.8±8.5, P<0.05). In addition, frozen-thawed sperm at 8 months of age showed low total motile sperm compared to those at 13, 14 and 15 months of age (26.4±8.2 vs. 45.7±29.5, 62.3±41.0, 70.4±15.9%, respectively; P<0.05). In conclusion, sperm derived from epididymal tail at 8 months of age in Hanwoo bulls showed high abnormal morphology and poor motility, which is not adequate for artificial insemination(AI) and in vitro fertilization(IVF). On the other hand, sperm derived from epididymal tail at 13, 14, 15 months of age in bull showed high normal morphology and motility, which may be available for AI and IVF. Epididymal sperm collected from bulls over 13 months is needed for further study whether to use the actual in vitro fertilization.

Semen collection from epididymis has been used as an important alternative tool, particularly on abnormal animals including those with joint disorder, poor sex drive and poor libido. However, previous studies had been focused on only recovery of sperm derived from testes, regardless of fundamental parameters such as age, body weight, scrotal circumference, testicular size (weight, length, width and volume) and semen volume. In addition, there is no precise castrating periods to recover sperm from young Hanwoo bulls’ testis. Therefore, we investigated fundamental parameters in Hanwoo bulls at 7, 8, 14, 15, 16 and 17 months of age, which parameter can be used for sperm recovery from testis. Before castration, body weight and scrotal circumference were recorded. After castration, testes were transported to laboratory and testicular weight, length and width were recorded. About 2 cm of epididymal tail was collected and minced using blades on 100 mm petridish. Minced epididymal tail tissues were mixed with Optixcell (France, IMV technologies) and debris were removed by filteration with 100 um nylon mesh. Seven to 8 months of age in bulls showed low fundamental parameters compared to those of at 14 to 17 months of age in bulls (body weight, 218-258 vs. 330-429 kg; scrotal circumference, 23.4-24.6 vs. 28.8-32.8 cm; testicular weight, 92-104 vs. 222.3-269.9 g; testicular length, 10.9-11.6 vs. 13.4-15.6 cm; testicular width, 4.7 vs. 6.2-6.6; testicular volume, 126.4-136.4 vs. 268.9-357.6 cm3, semen volume, 3.0-4.8 vs. 60.6-68.3 ml, p<0.001). In conclusion, to recover semen derived from epididymis of testis in young Hanwoo bull, these fundamental parameters should be satisfied; 330 kg of body weight, 28.8 cm of scrotal circumference, 222.3 g of testicular weight, 13.4 cm of testicular length, 6.2 cm of testicular width, 268.9 cm3 of testicular volume. In further study, fundamental parameters of 9 to 13 months of age in bull should be investigated to determine more accurate castrating periods for sperm recovery from testis.

The recovery of epididymal sperm in animals is considered as one of the important tools to preserve high value or endangered species. However, there are no appropriate castrating indicators such as months of age in bull, sperm morphology, and motility, particularly in young Korean native bull (Hanwoo). Therefore, this study aimed to investigate sperm number, morphology, and motility of sperm in the epididymis tail of young Hanwoo bulls at 8 and 15 months of age. After castration, epididymal tails were collected and minced with blades to recover sperm. In experiments 1 and 2, sperm number, morphology, and motility were examined. Total number of sperm and percentage of normal sperm from bulls at 8 months of age was lower than that of bulls at 15 months of age after collection (P<0.05). Percentage of abnormal head, tail, proximal cytoplasmic droplet, dead and damaged acrosome of sperm from bulls at 8 months of age were higher than those of bulls at 15 months of age (P<0.05). In experiment 3, sperm motility from bulls at 8 and 15 months of age were examined before freezing and after thawing. Frozen-thawed sperm at 8 months of age showed low total motility and motile sperm with ≥ 25 μm/sec compared to those at 15 months of age and commercially-used sperm (P<0.05). In conclusion, sperm derived from the epididymal tail of bulls at 8 months of age showed high abnormal morphology and poor motility, which are not adequate for AI and IVF. On the other hand, sperm derived from the epididymal tail of bulls at 15 months of age showed high normal morphology and motility.

본 연구에서는 한우 보증씨수소 KPN 493, 586, 614, 632, 666을 암소에게 인공 수정하여 생산된 자손 축 총 60두(5처리×12두씩/처리구당)에 대한 육질의 이화학적 특성과 상관관계를 분석하였다. 등심 면적 및 근내지방도는 KPN 586 자손축이 가장 우수하였으며(p<0.05), 육질의 이화학적 특성에서는 처리구 간에 거의 차이가 없었으나 특히 풍미와 육색의 황색도(b값)가 KPN 493이 가장 좋았다(p<0.05). 지방산중 올레인산은 KPN 493은 가장 높았다(p<0.05). 또한 각 형질별 상관관계에서, 도체중과 등심 단면적, 등심 단면적과 근내지방도에서 정(+)의 상관관계를 나타내었고(P<0.01), 보수력은 수분과 조단백질 함량에서 부(-)의 상관관계를 나타내었 (P<0.01). 또한 연도는 다즙성과 정(+)의 상관관계, 풍미는 다즙성, 연도 간에 정(+)의 상관관계, C18:1n9과 C20:1n9와 불포화 지방산 간에는 정(+)의 상관 관계를 나타내었다(P<0.01).

The conception rate of cow is a major factor in farm management. The environment of farm and management of cow are the best influencing factors on conception rate, and the fertility of bull is the second influencing factor. In Hanwoo bull, however, the informations limited to performance and carcass traits have been offered to Hanwoo farmer. Therefore, this study analysed the estimated relative conception rates (ERCR) for estimation of fertility of bulls, using the 8,892 mating data with 116 heads of prove bull to produce progeny. Mean of least square means of conception rate after first insemination was 50.95% in bull herds. On the standard of this mean, ERCRs after first insemination of each bull were analysed. Values ranged from -26.1% to +21.0%, the difference was 47.1%. Among 116 heads of bull analysed, KPN582 showed the highest ERCR as 21.0%, KPN550 (18.3%), KPN656 (16.7%), KPN632 (15.8%), KPN690 (14.9%) were gone behind, but KPN621 was the lowest as -26.1%, KPN680 (-21.3%), KPN674 (-16.2%), KPN569 (-15.9%), KPN699 (-14.9%) were succeeded. If ERCRs of Hanwoo bull will be offered to Hanwoo farmer, it will be worthwhile.

한우 종모우에 있어 정액 채취시 승가 조건(의빈우 혹은 의빈대)이 정액성상에 미치는 영향을 구명하기 위하여 의빈우 승가 종모우 21두, 의빈대승가 종모우 9두 등 보증 종모우 30두를 공시하여 연구하였다. 정액은 일 간격으로 채취하였으며 채취 당일 1시간 간격으로 총 2회 정액 채취하여 6개월간 정액성상을 조사하였다. 의빈대 승가 종모우가 의빈우 승가 종모우보다 1차 및 2차 정자농도에 있어 유의적으로 높아(p<0.05) 1차 및 2차 총 정자수에서도

This study was undertaken in an effort to select the sire bull in Hanwoo through in vitro fertilization of proven bull semen. It was used for in vitro fertilization that of the 20 proven bull semen with follicular oocytes derived from slaughterhouse ovaries of Hanwoo. The stage of maturation on the time course of bovine cumulus-enclosed oocytes incubated for 24 hours was found the highest(96.4%) than hose of other maturationi time. In vitro fertilization rate of bovine oocytes with proven bull sperm showed from 61.5 to 88.9%. Polyspermy of in vitro fertilized oocytes according to proven bulls were the highest KP 491(61.5%) nothing but KP 486, KP 491 and KP 497.

This study was conducted to compare among bull, steer and heifer on growth performance, blood composition and carcass traits according to fattening phase in Hanwoo. 12 month of aged 4 bulls (339.8±18.5 kg), 4 steers (309.8±13.2 kg), and 3 heifers (290.0±16.7 kg) were allocated in the stalls with individual feeding system during 20 months. Average daily gain was not different among the treatment groups during early fattening phase, but higher in the bulls and lower in the heifers after mid-fattening phase (p<0.05). The difference of body size by animal groups appeared from 24 month of age, and wither height and body length of Hanwoo heifer were the smallest (p<0.05) among treatment group. But wither height was not difference among treatment groups at 32 month of age. At 12 month of age, concentrations of serum cholesterol, triglyceride, glucose and total protein were higher in the heifers compared to other groups, and serum GPT (Glutamic pyruvic transaminase) was the highest (p<0.05) in the bulls, and serum GOT (Glutamic oxaloacetic transaminase) was the highest (p<0.05) at late fattening phase in the bulls. Meat yield index was similar between the bulls and the heifers, and the lowest (p<0.05) in the steers. Marbling score was significantly higher (p<0.05) in the steers and the heifers than in the bulls, and meat quality was the best in the steers among treatment groups. The results of this experiment might be used as a basal data on difference between gender in revision of Korean feeding standard for Hanwoo.