• 한국가축번식학회지
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• 제17권2호
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• pp.141-148
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• 1993

This studies were carried out to investigate the effects of co-culture with cumulus cells, oviduct epithelial cells and uterine endometrium cells on the in-vitro fertilization and cleavage rate of bovine follicular oocytes. The ovaries were obtained from slaughtered Korean native cows. The follicular oocytes surrounded with cumulus cells were recovered by aspirating follicular fluids from the visible follicles of diameter 3~5 mm. The follicular oocytes were cultured in TCM-199 medium containing hormones and 10% FCS for 24~48 hrs in a incubator with 5% CO2 in air at 38.5$^{\circ}C$ and then matured oocytes were again cultured for 12~18 hrs with motile capacitated sperm by preincubation. The results obtained in these experiments were summarized as follows: 1. The in vitro maturatin and fertilization rate of bovine oocytes co-cultured with cumulus cells in TCM-199 medium were 64.0~74.1% and 40.0~58.6% respectively. And in-vitro fertilization rate of cumulus-enclosed oocytes(55.4%) were significantly(p<0.05) higher than cumulus-denuded oocytes(23.1%). 2. The in-vitro maturatin and fertilization rate of bovine oocytes co-cultured with 1$\times$104 cells/ml, 1$\times$106 cells/ml, 1$\times$108 cells/ml and 1$\times$1015 cells/ml oviduct epithelial cells in TCM-199 medium were 59.3% and 40.7%, 64.0% and 48.0%, 58.3% and 37.5%, 52.0% and 32.0%, respectively. 3. The in-vitro maturation and fertilization rate of bovine oocytes co-cultured with 1$\times$104 cells/ml, 1$\times$106 cells/ml, 1$\times$108 cells/ml and 1$\times$1015 cells/ml uterine endometrium cells in TCM-199 medium were 56.0% and 36.0%, 60.7% and 42.9%, 59.3% and 37.0%, 52.0% and 36.0%, respectively. 4. When the in-vitro fertilized oocytes were co-cultured with cumulus cells, oviduct epithelial cells and uterine endometrium cells, the development rate to be blastocyst was 12.2%, 15.6% and 11.7%, respectively and rates were higher than that of control, 2.1%(P<0.05).

• Journal of Animal Science and Technology
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• 제44권5호
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• pp.561-572
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• 2002

본 연구는 분만전후 40두의 젖소에 무첨가, Aspergillus oryzae(T2), Saccharomyces cerevisiae 혼합제(T3) 및 효소분비촉진제(T4) 급여시 사료섭취량, 산유량 혈중대사물질 및 대사성 질병에 발생에 미치는 영향을 구명하기 위하여 완전임의배치법 10반복으로 수행하였다. 주요 연구결과는 다음과 같다. 분만전 건물섭취량은 처리간에 별 차이가 없었지만 분만일과 분만후 3주 동안에는 Aspergillus oryzae, Saccharomyces cerevisiae 혼합제 및 효소분비촉진제를 급여했을 때가 대조구보다 다소 많았다. 산유량은 사료첨가제를 급여한 구가 무첨가구보다 더 높았으며 특히 효소분비촉진제에서 산유량이 가장 높았다. 혈중 글루코스 및 NEFA 함량은 분만전에는 처리간에 큰 차이가 없었지만 분만일과 분만후 1, 2 및 3일에는 사료첨가제 급여구에서 대조구보다 혈중 글루코스 함량은 더 높고 반면에 NEFA 함량은 더 낮았다. 혈중 Ca 수준은 시험기간동안 처리간에 차이가 없었다. 대사성질병 발생은 대조구에서만 케토시스 1두 발생하였으며, 후산증체는 효소분비 촉진제구는 전혀 발생하지 않았으나 다른 구에서는 공히 2두가 발생하였다. 자궁 내막염은 T2구에서 1두 발생하였다. 결론적으로 전환기 젖소에 사료첨가제를 급여하면 사료섭취량 및 산유량 증가와 더불어 대사성질병 발생이 저하될 것으로 사료된다.

• Clinical and Experimental Reproductive Medicine
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• 제21권1호
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• pp.43-48
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• 1994

To evaluate the effectiveness of GnRH agonist for the treatment of uterine myoma as a cause of infertility, fourteen women were recruited to the study. The patients were treated with a delayed-release formulation of D-$Trp^6$-LHRH in biodegradable microcapsules(Decapeptyl-CR), administered intramuscularly at four week intervals for a period of six monthes. The first injection was given on day 21 of the cycle. Serum estradiol levels fell significantly to the mean value of 257.7pgjml 4 weeks after the first injection. Eleven patients in fourteen treated patients had a reduction in the size of uterine myoma as assessed by ultrasonography, two patients had no change of size and one patient had a increase of size. After the first or second injection, all patients became amenorrheic, then resumption of menstruation ocurred at 12 to 14 weeks after the last injection. Common side effects were hot flush, sweating and dyspareunia, whitch were acceptale. In Eleven patients who had a reduction in the size of uterine myoma by treatment with a delayed- release formulation of D-$Trp^6$-LHRH(Decapeptyl-CR), after above treatment with GnRH agonist, then four patients were treated with myomectomy, three patients had pregnancy and full term delivered by Cesarean section. These data suggest that administration of a delayed-release formulation of a GnRH agonist can be a worthwhile and convenient approach to the medical treatment of uterine myoma as a cause of infertility.

• Journal of Yeungnam Medical Science
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• 제16권1호
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• pp.52-59
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• 1999

미숙아의 여러 가지 합병증 중에서도 선생아 호흡 곤란 증후군은 가장 빈도가 높고 사망률도 높은 질병이다. 이제까지 많은 저자들이 자궁내 성장기 동안에 폐 표면 활성제 생성을 증가시킴으로써 신생아 호흡 곤란 증후군을 예방할 수 있는 약제로 corticosteroid에 대한 연구를 하였으나, 산모와 태아 감염에 중요한 위협 요인이 되어 이 약의 사용이 제한적이다. 따라서 steroid의 부작용 때문에 태아의 폐를 성숙시킬 수 있는 ambroxol에 관심을 가지게 되었으며 이에 저자들은 출생 전 산모에게 투여한 ambroxol이 신생아 호흡 곤란 증후군의 발생 빈도에 어떤 영향을 미치는지와 그 부작용에 대해 알아보고자 하였다. 1996년 1월부터 1997년 12월까지 영남대학교 의과대학 부속 병원 산부인과에 입원하였던 36주 이전의 조산이 예견된 산모에게 ambroxol(Mucosolvan$^{(R)}$, Boehringer Ingelheim) 1,000mg을 5% glucose 용액에 녹여 2시간 이상 정주하며 3일에서 5일간 투여하였다. 또한 대조군에서는 생리 식염수를 정주하였다. 조기 분만의 원인이나 대상 환아 평균 재태 연령, 남녀비, 출생 체중과 1, 5분 Apgar 점수가 7점 미만인 미숙아의 수에는 양 군간의 의미있는 차이는 없었다. 그러나 대조군에서는 21명 중 13명에서 신생아 호흡 곤란 증후군이 발생하였고 ambroxol 사용군에서는 21명 중 6명에서 신생아 호흡 곤란 증후군이 발생하여 두 군간에 의미있는 차이가 있었다(p<0.05). 출생 후 산소 치료와 인공 환기를 필요로 했던 경우는 대조군에서는 각각 18, 12명이었고 ambroxol 사용군에서는 각각 9, 8명이었다. 산소치료를 요구된 시간은 ambroxol 군에서 낮았으나 인공 환기가 필요하였던 시간은 ambroxol 군에서 더 길었다. 그 외 미숙아에게 나타난 주산기 합병증의 빈도는 ambroxol 사용군과 대조군을 비교해 보면 두 군이 같거나 ambroxol 군이 더 적었다. Ambroxol 투여 전과 후의 산모의 혈액학적, 생화학적 검사에 의미있는 변화는 없었다. 그리고 ambroxol 사용군에서 산모가 호소하는 부작용으로는 경미한 오심이 3례 있었으나 구토, 두통이나 현기증, 알레르기 반응 등은 나타나지 않았다. 그러므로 본 연구에서는 미숙아 출생 전 산모에게 투여한 ambroxol은 신생아 호흡 곤란 증후군의 발생 빈도를 감소시킨다고 생각되며 이를 위해 산모에게 안전하게 사용할 수 있는 약제로 생각된다.

• Journal of Nutrition and Health
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• 제39권4호
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• pp.331-337
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• 2006

청국장 분말이 고지방식이를 섭취한 흰쥐의 지질대사에 미치는 영향을 조사하고자, 성숙한 암쥐에 4주간 고지방식이(0.1% 콜레스테롤, 10% 지방)로 고지혈증을 유도한 후 대조군 (고지방식이), 청국장군 (고지방식이에 단백질원으로 청국장 분말을 첨가한 식이) 및 신령버섯 청국장군 (고지방식이에 단백질원으로 신령버섯 청국장 분말을 첨가한 식이) 등 3군으로 나누어 8주간 사육한 결과는 다음과 같다. 실험동물의 체중변화는 대조군은 16.1 g증가에 비하여 청국장군 및 신령버섯 청국장군은 각 1.0 g 및 5.9 g 증가로 유의하게 감소되었고, 식이섭취량 및 식이효율도 대조군에 비하여 청국장군들이 감소되었다. 자궁주위 지방의 무게 및 간조직의 콜레스테롤과 중성지질 농도는 대조군에 비하여 청국장군 및 신령버섯 청국장군이 유의하게 감소되었다. 혈청의 중성지질. 총 콜레스테롤, LDL-콜레스테롤 농도 및 동맥경화지수는 대조군에 비해 청국장군 및 신려버섯 청국장군이 유의하게 감소되었고, 총 콜레스테롤에 대한 HDL-콜레스테롤의 비율은 대조군에 비해 청국장군들이 유의하게 증가되었다. 변의 무게, 수분함량 및 총 지질 배설량은 청국장군들이 대조군 보다 유의하게 증가된 것으로 나타났다. 혈청 단백질 및 혈당 농도는 청국장 및 신령버섯 청국장 섭취에 의한 영향은 나타나지 않았으나, 혈색소 농도는 청국장군들이 증가되는 것으로 나타타났다. 이상의 결과로 보아 고지방식이에 청국장 및 신령버섯 청국장 분말 첨가 섭취시 흰쥐의 체중 감소와 혈청과 간조직의 중성지질, 총 콜레스테롤과 LDL-콜레스테롤 농도 및 동맥경화지수를 낮추고, 총 콜레스테롤에 대한 HDL-콜레스테롤의 비율이 증가되어 지질대사의 개선 효과가 있는 것으로 나타났다.

• 대한방사선치료학회지
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• 제1권1호
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• pp.70-78
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• 1985

The intrauterine irradiation is essential to achieve adequate tumor dose to centeral tumor mass in radio therapy for uterine malignancy. The complications of pelvic organ are known to be directly related to radiation dose and physical parameters. The comparison study of currently using 2 systems was undertaken. The simulation films and medical records of 135 patients who was treated with intrauterine irradiation at one of general hospitals in Busan and Seoul between Jan. 1983 and June 1983, were critically analized and physical parameters of low dose rate system and remote controlled high dose rate system were measured. The physical parameters include distances between lateral walls of vaginal fornices, longitudinal and lateral angles of tandem to the body axis, the distance from the external os of uterine cervix to the central axis of ovoids, the radiation dose ratio to rectum and bladder to reference point A. Followings were summary of study results: 1. In distances between lateral walls of vaginal fornices the low dose rate system showed wide distribution and relatively larger distances. In low dose rate system 5.0-5.9 cm was $55.89\%$ 6.0-6.9 cm: $23.53\%$, 4.0-4.9cm: $10.29\%$, 3.0-3.9cm: $10.29\%$, and in high dose rate system 5.0-5.9cm was $80.59\%$, 4.0-4.9cm: $17.91\%$, $6.0\~6.9\;cm:\;1.5\%$. 2. In lateral angulation of tandem to body axis, the low does system revealed mid position (the position along body axis) $64.7\%$, Lt. deviation $19.13\%$ and Rt. deviation $16.17\%$. However the high dose rate system revealed mid position $49.26\%$ Lt. deviation $40.29\%$ and Rt. deviation $10.45\%$. 3. In longitudinal angulation of tandem to body axis the mid position was $11.77\%$ and anterior angulation $88.23\%$ in low dose rate system but in high dose rate system the mid position was $1.56\%$ and anterior angulation $98.44\%$. 4. Down ward displacement of ovoids below external os was only $2.94\%$ in low dose rate system and $67.69\%$ in high dose rate system. 5. The radiation dose ration to rectum to reference point A was $102.70\%$ in high dose rate system and $70.09\%$ in low dose rate system. The dose ratio to bladder to reference point A was $78.14\%$ in high dose rate system and $75.32\%$ in low dose rate system.

• 대한방사선치료학회지
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• 제18권2호
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• pp.119-125
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• 2006

목 적: 본 연구에서는 근접치료 시 선량기준점에서 선량을 정확히 분석하고자 근접방사선치료용 다목적 팬텀(Multi Purpose Brachytherapy Phantom, MPBP)을 제작하여 그 유용성을 평가하고자 하였다. 대상 및 방법: 자체 제작된 근접방사선치료용 다목적 팬텀(MPBP)에서 다기능삽입구(Multi Function Applicator, MFA)를 이용하여 치료 시와 동일한 조건을 재현한 후 열형광선량계(TLD)를 이용하여 전산화 치료계획 장치에서 계산된 좌표와 동일한 기준점에서 선량을 측정하였다. 측정 대상은 근접방사선 치료환자 중 탄뎀(tandem)과 난형체(ovoid)를 사용한 자궁경부암 환자 4명을 대상으로 환자 당 5회씩 총 20회 A point와 B point 그리고 방광에서 선량을 측정하였다. 결 과: MPBP에서 TLD의 측정 결과는 A Point에서 측정한 환자의 상대오차가 각각 -3.2%, -0.2%, 0%, 3.8%를 보였고, B point에서는 -1.4%, -1.4%, 2.4%, 4.0%를 보였다. 그리고 방광에서는 1.3%, 2%, 5.4%, 7.15%의 상대오차를 나타내었다. 결 론: 자체 제작된 근접치료용 다목적 팬텀(MPBP)은 다기능삽입구(MFA)를 사용하여 치료 시와 동일한 조건에서 선량측정의 재현성을 이룰 수 있었고, A, B point지점과 방광의 선량을 정확히 분석할 수 있었다. 따라서 본 연구에서 제작된 근접방사선치료용 다목적 팬텀은 기준점 선량분석에 매우 유용한 것으로 판단된다.

• The Korean Journal of Physiology
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• 제21권1호
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• pp.35-46
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• 1987

It has been well known that estrogens stimulate the uterine contractility and progestins inhibit it. Then, one may expect that the uterine contractility and sensitivities to oxytocin (OT) and prostaglandin $F_{2{\alpha}}\;(PGF_{2{\alpha}})$ would be different among the estrus cycle. These hypotheses were tested using the mature female rat. Spontaneous isometric contractions of isolated uterine strips $(1{\times}0.3\;cm)$ from cyclic rats in various stages of the estrus cycle, bilateral ovarectomized rats and hypophysectomized rats were recorded in absence or presence with $estradiol-17{\beta}\;(E_2)$, progesterone $(P_4)$, OT and $PGF_{2{\alpha}}$. The results were summarized as follows: 1) The spontaneous uterine contractile force was the highest in the estrus rat and the lowest in the ovarectomized or the hypophysectomized rat. In the proestrus rat, the contractile frequency was the lowest (2.7 beats/10 min) and the contractile duration was the longest (70 sec). In the other groups, there were no any differencies in frequency (9 beats/10 min) and in duration (30 sec). 2) OT and $PGF_{2{\alpha}}$ stimulated the uterine contractility in all groups tested except in the hypophysectomized rat in which OT failed to stimulate the uterine contraction. $PGF_{2{\alpha}}$ was more effective in stimulating the uterine contraction than OT in all groups tested except in the estrus rat. OT-induced contraction was the highest in the estrus rat and $PGF_{2{\alpha}}-induced$ contraction was the lowest in the hypophysectomized rat. 3) Uterine contractilities were not changed by the in vitro treatments of $E_2$ or $P_4$ under the influence of endogenous steroids, however, $E_2$ and $P_4$ stimulated the uterine contraction in the ovarectomized rat in which endogenous steroids were almost abolished. 4) Increased uterine contraction by the treatment of OT was suppressed by in vitro $E_2$ or $P_4$ in the estrus rat, while it was potentiated by the $P_4$ in the proestrus rat. In other groups, exogenous $E_2$ or $P_4$ did not affect the OT-induced uterine contraction. 5) $PGF_{2{\alpha}}-induced$ uterine contraction was suppressed in the ovarectomized rat by $E_2$ and $P_4$, in the diestrus and proestrus rats by $P_4$ and in the hypophysectomized rat by $E_2$. In other groups, exogenous $E_2$ or $P_4$ was ineffective in altering the $PGF_{2{\alpha}}-induced$ uterine contraction. According to the above results, it may conclude that the mechanisms of the different uterine contractility and the different uterine sensitivity to OT or $PGF_{2{\alpha}}$ according to the estrus cycle are not explicable with only the serum concentrations of steroids, OT and $PGF_{2{\alpha}}$ but also other unknown factors.

• The Korean Journal of Physiology
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• 제18권1호
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• pp.37-50
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• 1984

The effects of $Ca^{++}$ and its antagonists (verapamil and $La^{+++}$) upon the spontaneous contraction and the contracture induced by 60 mM K-Tyrode solution were studied in the isolated uterine muscle. Longitudinal muscle strips were prepared from the rat uteri at estrous stage. All experiments were performed in tris-buffered Tyrode solution which was aerated with 100% $O_2$ and kept at 35^{\circ}$. The results obtained were as follows: 1) In the uterine strips contracting spontaneously, both the amplitude of peak tension and the area of contraction curve increased dose-dependently in the range of $0.5${\sim}8$ mM $Ca^{++}$. The frequency of contraction increased as the concentration of $Ca^{++}$ increased up to 2 mM, but above this concentration the frequency decreased. In $Ca^{++}-free$ media, however, contraction did not develop. In the contracture induced by 60 mM K-Tyrode solution, the developed tension increased dose-dependently as the concentration of external $Ca^{++}$ increased to 8 mM. In the absence of external $Ca^{++}$ K-contracture appeared, but it was not sustained. 2) The spontaneous contraction of rat uterus was suppressed by verapamil in proportion to an increase of its concentration and totally abolished at the concentration of $3{\times}10^{-4}\;g/l$, but the spontaneous contraction re-appeared by addition of $Ca^{++}$. The amplitude of peak tension recovered completely but the recovery of frequency was incomplete. K-contracture decreased in a dose-dependent manner after the treatment with verapamil and totally disappeared at its concentration of $3{\times}10^{-4}\;g/l$. Even in this case contracture developed again by extra $Ca^{++}$. 3) The spontaneous contractile activity was inhibited by $La^{+++}$. At the concentration of $10^{-4}$M $La^{+++}$, fibrillation appeared. In the strip inhibited by $10^{-5}M\;La^{+++}$, contractility recovered completely by extra $Ca^{++}$ while in the $10^{-4}M\;La^{+++}$ treated preparation, the rhythmic spontaneous contraction did not develop even at the concentration of 16 mM $Ca^{++}$. After the initial transient depression of contracture tension by $10^{-3}M$ of $La^{+++}$, the strip stowed considerably large size of contracture, hardly influenced by external $Ca^{++}$ or verapamil. The results obtained in this experiment suggest that in the rat uterine muscle there would be some competitive actions between $Ca^{++}$ and its antagonists. It is speculated that $Ca^{++}$ plays an important role in the conduction of excitation, and $La^{+++}$ influences upon cellular $Ca^{++}$ mobilization and re-uptake process as well as transmembrane $Ca^{++}$ transport in a K-depolarized state.

• 약학회지
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• 제48권6호
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• pp.328-334
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• 2004

Cervical cancer is one of the leading causes of female death. Viral oncoproteins E6 and E7 are selectively retained and expressed in carcinoma cells infected with HPV (Human pa pilloma virus) type 16 and cooperated in immotalization and transformation of primary keratinocyte. E6 and E7 oncoproteins interfere the functions of tumor suppressor proteins p53 and retinoblasoma protein (pRb), respectively. Among a lots of natural products, Mentha arvensis Linne var.piperascens have inhibitory effects on bindings between E6 oncoprotein and tumor suppressor p53, E3 ubiqutin- protein ligase (E6AP). HPV oncoprotein inhibitors from Mentha piperita L. were isolated by solvent partition and column chromatography (Silica gel, RP-18) and inhibitory compounds were finally purified by HPLC using an ELISA screening system based on binding between E6 and E6AP. The aim of this study is to identify the structure of inhibitory compounds and to investigate whether these compounds have inhibitory effects on functions of E6 oncoprotein. We investigated whether caffeic acid methyl ester (CAM) extracted from Mentha piperita L. could inhibit the function of E6 oncoprotein. CAM inhibited the in vitro binding of E6 and E6AP which are essential for the binding and degradation of the tumor suppressor p53 and also inhibited the proliferation of human cervical cancer cell lines (SiHa and CaSKi) in a dose response manner. These results suggest that CAM inhibited the function of E6 oncoprotein, suggesting that it can be used as a potential drug for the treatment of cervical cancers infected with HPV.