• 한국수정란이식학회지
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• 제13권1호
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• pp.77-86
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• 1998

A combined technology of transvaginal ovum pick-up(OPU) system with in vitro-oocyte manipulation technique can be used for improving reproductive efficiency in the cattle. The objective of this study was to establish a newly-conceived breeding program using OPU in the pregnant cows. The OPU trial was performed in pregnant cows every 10 days from 40 through 90 days of artificial insemination (Al), and number of follicles in ovary, number of retrieved oocytes and embryo development following in vitro-fertilization, were evaluated. Reduced number of follicles in the ovaries of pregnant cows was firstly detected from 70 days after A' and a significant (P<0.05) decrease in the follicle number (5.4 follicles /donor) was found at 90 days than at 40, 50, 60 and 80 days after Al (8.0~9.2). A similar pattern was also observed in the number of oocytes retrieved by OPU apparatus during experimental period. When retrieved oocytes were matured and inseminated in vitro with frozen bull semen, development of the oocytes to the blastocyst stage was not significantly affected by the retrieval time. Four embryos (morula or blastocyst stage) derived from oocytes retrieved from pregnant cows were nonsurgically transferred to four recipient cows on day 7 of estrus cycle. For the first time in Korea, three of four transferred embryos developed to live calves with normal physiological parameters. In conclusion, an effective breeding program employing pregnant cow can be developed by use of OPU trial and in vitro culture techniques of oocytes ; OPU system could be repeated in pregnant cows with no risk of abortion and viable offsprings were borne after transfer to the recipients.

• 한국수정란이식학회지
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• 제27권4호
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• pp.265-270
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• 2012

In canine, oocytes are ovulated at the GV (germinal vesicle) stage and they have to fulfill maturation phase before reaching metaphase II stage. The efficiency of in vitro maturation is still very low. Therefore, the aim of this study was to investigate the effect of in vitro maturation on nuclear changes of immature canine oocytes recovered from different reproductive stages ovaries and different culture conditions. The oocytes were cultured in TCM-199 with supplement at 5% $CO_2$ and $38.5^{\circ}C$ for 72 h. The nuclear maturation of canine oocytes was evaluated with Hoechst 33342 stain under fluorescence microscope (Fig. 1). The results of this study detected differences in in vitro maturation rate between oocytes recovered from follicle status and non-follicle status ovaries. However, these differences were not significant as indicated in Table 1 and Fig. 2. In regard to the effect of culture condition with supplements, we did not found significant differences compared with control group (Table 2, Table 3). One of the reasons for this data could be the conditions that ovaries were exposed during slaughtering process or the long distant transportation of the ovaries. Although these data have not shown clearly significant differences results compared with control, furthermore the different reproductive status ovaries was beneficial for maturation of oocytes in vitro and can be a basic part of knowledge to improve in vitro maturation of canine oocytes.

• 대한수의학회지
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• 제49권1호
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• pp.23-34
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• 2009

This study was performed to evaluate repeated-dose oral toxicities of Chelidonium majus extract in Fischer 344/N rats. Chelidonium majus extract was administered orally to rats at dose levels of 0, 25, 74, 222, 666 and 2,000 mg/kg/day. Each group consisted of 10 rats of each gender. The Chelidonium majus extract was given once a day, 5 times a week, for 90 day repeatedly. This study was conducted in accordance with the Protocol of Korea National Toxicology Program (issued by National Institute of Toxicological Research) and The Standards of Toxicity Study for Medicinal Products (issued by Korea Food and Drug Administration). In the present study, There were no toxicologically significant changes in mortality, clinical signs, body weight gains, ophthalmoscopy, urine analysis, hematology, serum biochemistry, necropsy findings, organ weights, histopathology, estrus cycle and sperm examination of all animals treated with Chelidonium majus extract. These results suggest that the oral no observed adverse-effect level of the test item, Chelidonium majus extract, in rats is higher than 2,000 mg/kg/day in both genders. The target organs were not established.

• Reproductive and Developmental Biology
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• 제33권3호
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• pp.157-162
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• 2009

This study was performed to comprehend the developmental characteristics of cloned embryos knocked out (KO) of $\alpha$-1,3-galactosyltransferase (GalT) gene. Immature oocytes were collected and cultured for 40 hrs (1-step) or 20hrs (with hormone) + 20hrs (without hormone) (2-step). The embryos transferred with miniature pig ear fibroblast cell were used as control. The reconstructed embryos were cultured in PZM-3 with 5% $CO_2$ in air at $38.5^{\circ}C$ for 6 days. To determine the quality of the blstocysts, TUNEL and quantitative realtime RT-PCR were performed. The embryos were transferred to a surrogate (Landrace) at an earlier stage of the estrus cycle. The maturation rate was significantly higher in 2-step method than that of 1-step (p<0.05). The blastocyst development of GalT KO embryos was significantly lower than that of normal cloned embryos (p<0.05). The total and apoptotic cell number of GalT KO blastocysts was not different statistically from control. The relative abundance of Bax-$\alpha$/Bcl-xl ratio was significantly higher in both cloned blastocysts than that of in vivo blastocysts (p<0.05). Taken together, it can be postulated that the lower developmental potential and higher expression of apoptosis related genes in GalT KO SCNT embryos might be a cause of a low efficiency of GalT KO cloned miniature pig production.

• Journal of Animal Science and Technology
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• 제66권3호
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• pp.577-586
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• 2024

The in vitro maturation (IVM) rate of canine oocytes remains low compared to other mammals due to their unique reproductive characteristics. This study aimed to explore the effect of hormone supplementation during the IVM of canine immature oocytes on nuclear maturation and subsequently assess its potential application in canine somatic cell nuclear transfer (SCNT). Immature oocytes were collected and cultured in an IVM medium supplemented with hormones (follicle-stimulating hormone [FSH] and progesterone [P4]) or without hormones (control) for 24 hours. The maturation rates of oocytes in the hormone-treated group (94.92 ± 3.15%) were significantly higher than those in the control group (61.01 ± 4.23%). Both in vitro and in vivo matured oocytes underwent NT to evaluate their utility, and the fusion rates were higher in the in vitro matured group than those in the vivo matured group, not significant between in vivo and in vitro matured group (73.28% and 82.35%, respectively). As a result, 14 fused embryos from the in vitro matured group were transferred into two surrogates, with one surrogate achieving a successful pregnancy and delivering four puppies. Whereas in the in vivo matured group, 85 fused embryos were transferred to 8 surrogate mothers, leading to three surrogates becoming pregnant and delivering one, four, and two puppies. The pregnancy rates were not significant between both groups (50% and 37.50%), but the number of offspring exhibited a significant difference (28.57% and 8.23%). In conclusion, we achieved a remarkable milestone by successfully producing cloned puppies using in vitro matured oocytes, underscoring the feasibility of canine cloning from in vitro recovered oocytes. It is important to note that this study focused only on immature oocytes after ovulation and only during the estrus stage. Further research targeting other stages of the estrous cycle could potentially enhance canine cloning efficiency.

• 한국가축번식학회지
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• 제23권2호
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• pp.175-180
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• 1999

본 실험은 한우 번식장애우와 저수태우의 혈액 성분 및 성선호르몬(estrogen과 progesterone)의 농도를 비교 분석하여 번식우의 기초적인 생리지표를 확립시키는데 있다. 본 실험의 결과를 요약하면 다음과 같다. 1. 저수태 한우와 번식장애우 혈중 albumin, BUN, Ca, cholesterol, creatine, glucose, phosphorous, total protein 및 triglyceride 함량은 3.28$\pm$0.05 와 3.27$\pm$0.04 g/㎗, 11.07$\pm$0.61와 12.69$\pm$0.88 mg/㎗, 9.98$\pm$0.10와 9.56$\pm$0.11mg/㎗, 105.75$\pm$3.57와 126.78$\pm$5.66 mg/㎗, 1.62$\pm$0.05와 1.65$\pm$0.09 mg/㎗, 67.46$\pm$3.07와 76.97$\pm$3.76 mg/㎗, 6.13$\pm$0.36 와 6.11$\pm$0.26 mg/㎗, 5.82$\pm$0.08와 6.18$\pm$0.08 g/㎗ 및 12.82$\pm$1.46와 15.19$\pm$1.61 mg/㎗으로 나타났다. 2. 혈청의 중요한 성분중 하나인 요소태 질소, 칼슘 및 인의 함량이 번식 장애우와 저수태우의 경우 정상우보다 다소 높은 경향을 나타냈으며, 특히 콜레스테롤의 함량이 번식 장애우와 저수태우의 경우 정상우의 약 2배정도 현저히 높은 성적을 나타냈다. 3. 발정주기중 혈액내 progesterone 수준은 임신우와 비임신우에서 수정후 18일까지는 비슷한 수준(6.55$\pm$0.17, 5.46$\pm$0.18 ng/$m\ell$)을 보였으나 그 후 임신우에서는 점차 증가하였고 비임신우에서는 발정일 (0.18$\pm$0.03 ng/$m\ell$)에 급감하였다. 4. 번식 장애우와 저수태우의 혈중 estrogen과 progesterone 함량은 각각 57.42$\pm$5.03, 56.76$\pm$8.73 pg/$m\ell$과 6.26$\pm$0.83 ng/$m\ell$, 9.41$\pm$1.85 ng/$m\ell$으로서, 혈중 progesterone 농도가 정상우의 황체기 수준으로 유지되어 발정발현과 수태가 억제되는 것으로 나타났다.

• 한국발생생물학회지:발생과생식
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• 제6권2호
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• pp.105-110
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• 2002

포유동물의 생식을 조절하는 다수의 호르몬 가운데 가장 중요한 것들로 난소로부터의 estrogen과 progesterone을 들 수 있다. 반면 다양한 스트레스 인자들은 암컷의 성 반응 행동과 번식을 억제함이 잘 알려졌다. 이러한 스트레스가 가해지는 동안 부신에서는 카테콜아민(catecholamine)이 다량 분비되어 위기 상황에 대처하며 이 과정에서 생식 현상의 억제가 일어나는 것으로 추정된다. 본 연구에서는 생식호르몬 분비와 성 행동 양식에 광범위한 영향을 미침이 알려진 카테콜아민 중 특히 부신의 norepinephrine(NE)과 epinephrine(E) 합성ㆍ분비 양상과 발정주기 간의 상관관계를 조사하였다. 이를 위해 HPLC-ECD를 사용하여 주기 중인 흰쥐 부신 수질내 NE와 E함량과 체외 배양한 부신으로부터의 분비를 조사하였다. NE 함량은 proestrus에서 증가하기 시작하여 diestrus I에서 최고에 도달하였고, diestrus II에 최소치로 감소하였다. 부신 내 E 함량의 최고치는 proestrus, 그리고 최저치는 diestrus II에서 관찰되었다. 흰쥐 부신 내 NE : E ratio는 diestrus I에서 1 : 4.81로 가장 낮았고 기타 시기에는 1 : 6.13～7.02였다. 체외 배양한 흰쥐 부신으로부터의 NE 분비는 diestrus II에서 가장 낮았으며 estrus에서 최고에 도달하였고, proestrus에서의 분비 역시 diestrus II 때보다 유의성있게 높았다. E분비의 최고치는 estrus에서, 그리고 최저치는 diestrus 떼서 II 관찰되었다. 한편 배양액 중 Ne : E ratio는 estrus에서 1 : 3.32로 가장 높았고 기타 시기에는 1 : 2.34～2.65였다. 본 연구 결과는 (1) 흰쥐 부신에서 카테콜아민 생성과 분비 양상이 발정주기 중 역동적으로 변화하며, (2) NE로부터 E로의 전환이 발정주기 중 stage-specific하게 일어남을 나타내는 것으로서, 이는 카테콜아민 합성율을 결정하는 rate limiting enzyme인 tyrosine hydroxylase(TH)와 NE에서 E로의 전환 과정을 매개하는 phenylethanolamine-N-methyltransferase(PNMT)의 발현과 활성이 중추신경계에서와 유사하게 생식호르몬, 특히 estrogen and/or progesterone의 영향을 받음을 시사한다.

• 한국수정란이식학회지
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• 제2권1호
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• pp.36-46
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• 1987

The present work was designed to understand the mechanism of superovuiation and the cause of early embryo loss and Implantation failure in the superovulating immature female rats which were elaborated by a pituitary gland transplantation. A pituitary gland obtained from the orchidectomized rats was transplanted under the right kidney capsule of 28 day old female rats (PGT group) on the starting day of experiment which was designated as Day 2. The grafted pituitary glands were removed at 6h (RPGT 6h group), 12h (RPGT 12hgroup) and 24h (RPGT 24h group) after the transplantation. Control rats were treated with 41U PMSG on Day 2 (PMSG group). The estrous cycle and the levels of plasma progesterone and estradiol-17$\beta$ were observed on Day 0, Day 5, respectively. The implantation sites, the weights of ovary and uterus, and the number of corpora lutea were examined in all group on Day 8. The resuft obtained were summarized as follows: 1. The percentages of the number of the rats in proestrus and estrus were 93.0%, 82.6%, 0%, 90.7% and 89.5% in PMSG, PGT, RPGT6h, RPGT12h and RPGT24h group, respectively. The synchronization of estrus cycle was dchieved in all groups. 2. The mating rates of each group were 80.2, 75.0, 0, 56.4, 57.8% in PMSG, PGT, RPGT6h, RPGT12h, RPGT24h group, respectively. 3. The numbers of copora lutea on Day 8 were 47.1 i 4.9, 18.1 $\pm$0.5, 14.1 i 0.3 and 8.9 $\pm$ 0.3 in PGT, RPGT24h, RPGTl2h and PMSG group, respectively. There were signIficantly difference between all groups (P<0.05). 4. The numbers of implantation sites (18.1 +- 4.0) in PGT group on Day 8 were higher than those of PMSG (8.5 $\pm$ 2.5), RPGT 12h (9.8 i 0.2) and RPGT 24h group (10.8 i 0.2) (P<0.05). 5. The ovarlan weights in PGT (95.2 $\pm$ 14.3mgIlOOg BW), RPGT 12h (51.7 $\pm$ 0.6mgIlOOg BW), and RPGT24h (57.9 $\pm$ 0.9mg/l00g 8W) groups were significantly higher than those of PMSG group (30.4 $\pm$7.4mg/l00g BW) (P<0.05). 6. The uterine weights in PMSG (672.4 $\pm$ 4.7mg/l00g 8W), and PGT (660.7 $\pm$7.8mg/l00g BW) groupswere greater than those of RPGT 12h (403.0 $\pm$ 1.lmg/lOOg BW) and RPGT 24h (490.1 $\pm$ 0.9mg/l00g BW) group (P<0.05). 7. The plasma progesterone levels in PGT groups (15 lng/ml) on Day 5 were higher than those of PMSG (83ng/ml), RPGT 12h (S7ng/ml), RPGT24h (8lng/ml) group (P<0.05). 8. The plasma estradiol-17$\beta$ levels in PMSG group (lBSpg/ml) on Day S were higher than those of RPGT 24h (l3pg/ml) group (P<0.05). But estradiol-17$\beta$ levels in PGT and RPGT 12h group were too low to discuss.

• 한국수정란이식학회지
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• 제24권3호
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• pp.151-157
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• 2009

Serial ultrasonography was conducted on Miniature Schnauzer bitches, on purpose to observe the ultrasonographic appearance of normal ovaries and ovarian structures during the estrous cycle. The size of ovaries was increased from $76.8{\pm}7.5mm^2(Mean{\pm}S.D)$ on Day-12 (Day-0=ovulation day) to $114.4{\pm}5.5mm^2$ on Day-8 and there was no significantly different between both ovaries. The ovaries were recognized by its proximity to the caudal renal pole and appeared moderately echogenic oval shape with a smooth contour. The size of follicles was increased from $8.1{\pm}4.5mm^2$ on Day-12 to $114.4{\pm}5.5mm^2$ on Day-0 and there was no significantly different between both ovaries. The number of follicles was increased from $2.8{\pm}0.7$ on Day-12 to $1.1{\pm}0.1$ on Day-0 and there was no significantly different between both ovaries. The follicles were small anechoic fluid-filled structures in early of proestrus, more increased, and indistinguished from each follicles in late of proestrus. The size of corpora lutea was increased from $19.3{\pm}2.1mm^2$ on Day-0 to $26.4{\pm}8.1mm^2$ on Day-8 and there was no significantly different between both ovaries. The number of corpora lutea was increased from $1.4{\pm}0.6$ on Day-0 to $2.9{\pm}0.4$ on Day-38 and there was no significantly different between both ovaries. The corpora lutea were small anechoic cavity and thin hyperechoic wall in early of diestrus, became more hyperechoic, and increased homogenous structures. The results of this study would be useful for differential diagnosis between normal and abnormal structures of ovaries.

• 한국가축번식학회지
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• 제17권2호
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• pp.165-171
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• 1993

Ornithine decarboxylase(ODC)가 polyamine 생합성에 주요 효소로 역할을 하지만 difluoromethylornithine(DFMO)은 polyamine 합성에 억제자로 작용하고 있다. Cycling crossbed gilt들을 무작위로 두 그룹으로 분배하였다(6/group). Indwelling silicone catheter를 모든 동물의 경정맥에 수술을 통해 이식하였다. DFMO는 생리식염수(20mg/ml)에 용해하여 매일 80mg/kg을 i.m.으로 주사하였으며 대조구에게는 같은 양의 생지식염수만을 주사하였다. DFMO는 estrous cycle day 16일부터 21일 혹은 발정때까지 하루 3번(08:00, 16:00, 24:00h) 주사하였다. Day 14일 부터 마지막 DFMO주사 이틀 후까지 하루 한번씩 10ml의 혈액을 채취하였다. Day 16일부터 21일까지 매일 다른 gilt로부터 8시간 동안(08:00∼16:00h) 15분 간격의 주기로 window 혈액을 채취하였다. Serum으로부터 progesteron(P4), Estradiol(E2), LH 및 FSH를 측정하였다. P4와 E2는 DFMO처리에 관계없이 follicular phase동안에 전형적인 profile을 보였다. DFMO처리는 발정직전의 LH농도를 저하시켰지만 (p<0.01), FSH에는 아무런 영향을 미치지 않았다. 결론적으로 gilt에 있어서 DFMO는 LH분비에 억제적인 영향을 미치는 한편, P4, E2 및 FSH에는 별로 영향을 미치지 않음이 나타났다.