• 한국동물학회지
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• 제32권3호
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• pp.264-274
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• 1989

본 실험은 생쥐에서 부정소액내의 단백질 성분과 조성에 미치는 정소액과 정자의 영향을 알아보기 위하여, 성적 성숙시기에 따라 정소와 부정소의 조직분화 양상을 관찰하였으며, 강소분화 특징에 따라 체취한 부정소액은 전기영동법으로 단백질을 분석하여 다음과 같은 결과를 얻었다. 정소와 부정소는 생후 10일군에서 미분화 상태였고, 20일군에서 세정관의 강소는 형성되지 않았으나 부정소는 두부에서 미부에까지 강소가 형성되었으며, 35일군에서는 정소내 세정관의 강소가 형성되었고 정세포는 정자로 분화되었고, 부정소의 상피세포는 principal cell과 clear cell로 분화되었으나 부정소로 유입된 정자는 없었다. 80일군에서는 정소와 부정소가 완전히 본화되었고 부정소로 유입된 많은정자가 관찰되었다. 그리고 부정소액의 전기영동상에는 혈청내의 성분과 다른 단백질이 모두 28종이 나타났는데, 그 중 12종은 부정소액에만 존재하는 부정소 특이단백질이었고, 16종은 정소액에도 공통으로 존재하는 단백질이었다. 또한 이 단백질들은 성숙시기에 따라 종류가 다르게 나타났으며, 성체에서 나타난 3종의 단백질은 부정소의 부위에 따라 양적인 변화를 나타냈다. 이상의 결과로 보아 부정소액내 단백질의 성분과 조성은 정자를 포함한 정소액의 유입과 부정소 상피세포의 분비 및 흡수의 조절작용에 의하여 변화되는 것으로 사료된다. 따라서 부정소액내의 TEP와 ESP는 부정소 정자의 성숙에 어떤 중요한 역할을 할 것으로 사료된다.

• Applied Microscopy
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• 제22권2호
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• pp.127-140
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• 1992

This research was undertaken to determine the effects of the cyclophosphamide (CP) on the epididymal corpus of the male rat in terms of ultrastructural alteration and protein analysis by SDS-PAGE at different groups; control group, 1 week group, 3 weeks group and 5 weeks group were treated with saline (control group) or CP at doses of 20mg/kg/week, 1 time a week, respectively. In the cytoplasm of the principal cells on the epididymal corpus, the mitochondria were significantly swollen or disrupted. The lumens of rough endoplasmic reticulum (rER) were also dilated and the number of secretory vesicles and lysosomes were increased respectively. CP caused changes in protein concentrations in the corpus of epididymis after CP treatment. Total proteins of 31 to 36 species were expressed in the corpus fluid. Then the more CP was increased, the more concentration of proteins caused to decrease, synthesize or increase in epididymal corpus. In contrast to the control group, in particular 88KD and the other 8 proteins in the corpus fluid, were decreased or disappeared respectively, whereas acid phosphatase and the other 9 proteins in the corpus fluid, were increased or synthesized respectively. The other proteins are not showed distinctive difference. It is suggested that treatment with CP alters the specific cell organelles and proteins in segment of the epididymal corpus.

• Clinical and Experimental Reproductive Medicine
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• 제24권1호
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• pp.27-34
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• 1997

This study aimed to evaluate the effect of seminal vesicle fluid (SVF) on the acrosome reaction (AR) occurred spontaneously or induced by $Ca^{2+}$ ionophore A23187, follicular fluid, and progesterone in mouse epididymal sperm. SVF was divided into high (MW>10 kD) and low (MW<10 kD) fractions by ultrafiltration. The low MW fraction of SVF decreased the rate of spontaneous AR, however the high MW fraction did not. It suggested that the low MW fraction of SVF might have contained decapacitation factor(s) responsible for prolonging of time need for capacitation. When sperm preincubated for 60 min in the presence of SVF, the rate of AR induced by A23187 was decreased, but prolongation of preincubation time for 120 min significantly potentiated the AR by A23187. It suggested that addition of SVF into sperm preincubation medium imposed the epididymal sperm a condition similar to ejaculation. AR induced by human follicular fluid or progesterone was also inhibited by SVF. It suggested that substance in SVF might have affected AR of mouse sperm by inhibiting the interaction between AR inducing ligands and sperm surface receptors involved in acrosomal exocytosis.

• Reproductive and Developmental Biology
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• 제30권4호
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• pp.301-305
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• 2006

The aim of this study was to investigate whether addition of porcine epididymal fluid (pEF) into culture medium during in vitro maturation influences the nuclear maturation of porcine germinal vesicle (GV) oocytes. Porcine cumulus-oocyte complexes (COCs) from follicles were cultured in tissue culture medium 199 (TCM 199) containing pEF. After 48hr of culture, oocytes were examined for evidence of GV breakdown, metaphase I, anaphase-telophase I, and metaphase II. The proportion of oocytes reaching at metaphase II (M II) stage was significantly (p<0.05) increased in oocytes cultured in the media supplemented with 10% pEF during in vitro maturation than in those without pEF regardless of cumulus presence or absence (54.6% vs 22.5%, 51.7% vs 24.2%). The supplementation of pEF during maturation of oocyte enhanced oocytes maturation in a dose-dependent manner in vitro. Also significant differences (p<0.05) in the percentage of MII oocytes were observed according to exposure period in pEF. Present study suggests that pEF contains a enhancing component(s) for nuclear maturation of porcine immature oocytes in vitro.

• Reproductive and Developmental Biology
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• 제33권3호
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• pp.125-131
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• 2009

The aim of this study is to investigate the effect of porcine epididymal fluid (pEF) on in vitro-maturation and subsequent fertilization of porcine follicular oocytes. Porcine cumulus-oocytes complexes retrieved from antral follicles were cultured in tissue culture medium (TCM)-l99 supplemented with pEF of different concentrations. At 48 h after culture, development of oocytes to germinal vesicle (GV) breakdown, metaphase I, anaphase-telophase I, and metaphase II were examined Significant (p<0.05) increase in the proportion of oocytes developed to MII stage was observed in oocytes cultured in pEF-containing TCM-l99 than in oocytes cultured in pEF-free TCM-199 (46.2% vs 16.7%), which was a dose-dependent manner. Subsequently, the proportion of monospermic fertilization were significantly (p<0.05) increased in oocytes cultured in the TCM supplemented with pEF than those cultured in pEF-free TCM-199 (51.0% vs 24.1%). In the second series of experiment, the percentage of MII oocytes was significantly (p<0.05) increased after exposure of oocytes to pEF during the first 22 h period of culture than after exposure of oocytes to pEF during the next 24 h of culture, while no significant difference in the percentage of monospermy was observed. The results of this study demonstrate that pEF contains at least enhancing component(s) for nuclear maturation.

• Childhood Kidney Diseases
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• 제1권1호
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• pp.86-90
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• 1997

The author experienced a case of $Henoch-Sch\"{o}nlein$ purpura with epididymitis in a 6-year-old boy who was admitted to our hospital due to left scrotal pain and the relapse of purpura on lower extremities for 3 days. Scrotal ultrasonography on admission revealed homogenously enlarged left epididymal head and small amount of fluid collection in left tunical space. The size of left epididymal head decreased gradually with no more evidence of fluid collection on day 7 and recovered completely on day 21. The author reports a case of $Henoch-Sch\"{o}nlein$ purpura with epididymitis with brief review of related literatures.

• Reproductive and Developmental Biology
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• 제32권3호
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• pp.147-152
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• 2008

The aim of this study was to investigate what components of porcine epididymal fluid (pEF) influences the nuclear maturation of porcine germinal vesicle oocytes. Porcine cumulus-oocytes complexes from follicles were cultured in TCM 199 containing pEF. After 48 h cultures, oocytes were examined for evidence of GV breakdown, metaphase I, anaphase-telophase I, and metaphase II. Maturation rate of oocytes was significantly increased in media supplemented with 10% pEF during in vitro maturation (IVM) than in those without pEF. When lipid component of pEF was removed by treating n-heptane, no significant difference was observed in maturation of oocytes between n-heptane treatrment and intact pEF group. However, the proportion of oocytes reaching at metaphase II (M II) was significantly (p<0.05) decreased in the oocytes cultured in media containing trypsin-treated pEF compared to those in media with intact pEF. When porcine GV oocytes were matured in the medium supplemented with intact pEF or pEF heated at $56^{\circ}C$ and $97^{\circ}C$, rates of oocytes remained at GV stage were 11.7%, 29.4% and 42.0%, respectively. However, there were no difference in proportion of oocytes reaching at MII stage among intact pEF group and $56^{\circ}C$ group. Present study suggests that 1) pEF contains an enhancing component(s) for nuclear maturation in vitro of oocytes, 2) protein(s) of pEF may be capable to promote nuclear maturation in vitro, and 3) enhancing component for nuclear maturation may consist of two factors, which are responsible for germinal vesicle breakdown (GVBD) and promotion of MII stage.

• Reproductive and Developmental Biology
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• 제34권4호
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• pp.275-281
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• 2010

The aim of this study was to investigate what protein(s) of porcine epididymal fluid (pEF) are able to enhance the nuclear maturation of porcine germinal vesicle (GV) oocytes in vitro. Proteins of pEF were fractionated by affinity, ion exchange, and gel filtration chromatography. Porcine cumulus-oocytes complexes (COC) from follicles were cultured in tissue culture medium (TCM 199) containing various fractions obtained by chromatography. Porcine COCs were also cultured in TCM 199 containing various meiosis inhibitors and pEF. After 24 or 48 h culture, oocytes were examined for evidence of GV breakdown, metaphase I, anaphase-telophase I, and metaphase II. When porcine COCs were cultured in the medium with meiosis inhibitor such as, dibutyryl cAMP (dbcAMP) and forskolin (Fo), more than 80% of oocytes were unable to resume meiosis. However, porcine COCs supplemented with pEF were able to overcome the inhibitory effect of dbcAMP and Fo. Maturation rate of oocytes was significantly (p<0.05) increased in the media supplemented with cationic protein(s) during in vitro maturation than in those with anionic protein(s) (44.1% vs 20.0%). When oocytes were cultured in the TCM 199 with fractions obtained by gel filtration, the maturation rate of oocytes was significantly (p<0.05) higher in fraction 11 containing 18 kDa than other fractions. The present study suggests that 1) dbcAMP and Fo prevent the spontaneous maturation of oocyte after isolation from follicles, and that pEF contain a substance(s) that improves meiosis resumption in vitro of porcine COCs, 2) cationic 18 kDa protein(s) are responsible for promotion of Mil stage.

• 한국가축번식학회지
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• 제26권2호
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• pp.105-110
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• 2002

본 연구는 소형견의 불임 해결과 번식효율 증진을 위해 소형견 난소 난포로부터 채취한 난자를 활성화 처리후 부고환 정자로 ICSI시켰을 때 체외발생율을 조사하기 위하여 수행하였다. 1. 난포란을 회수 후 24, 48시간 배양하였을 때 배양시간에 따른 GV, MI, MII로의 체외발생율은 각각 14/30(46.7%), 2/30(6.7%), 8/30(26.7%)였고 48시간 배양 시간에 따른 GV, MI, MII로의 체외발생율은 각각 l1/30(36.7%), 3/30(10.0%), 9/30(30.0%)였다. 2. 난포란을 회수 후 48시간 배양하였을 때 배양액에 따른 MII로의 체외발생율은 SOF액(10/30, 30.3%)에서의 배양이 TCM-199액(7/30, 23.3 %)보다 높은 체외발생율을 나타냈다. 3. 활성화 처리 난자에 부고환 정자로 ICSI를 하였을 때 상실배와 배반포로의 체외발생율은 각각 3/16(18.8%), 4/16(25.0%)로서 비활성화 처리 난자군의 3/13(23.1%), 1/13(7.7%)에 비해 높은 체외발생율을 나타냈다. 4. 활성화 처리 난자에 신선정자, 부고환 정자 및 동결 융해한 부고환 정자로 ICSI를 하였을 때 체외발생율은 각각 8/18(44.4%), 5/16(31.3%), 2/14(14.3%)로서 동결 부고환 정자 처리군은 신선정자 처리군에 비해 낮은 체외발생율을 나타냈다.

• 한국동물학회지
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• 제33권1호
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• pp.78-93
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• 1990

생쥐가 성숙하는 동안 부정소 상피세포의 분화와 부정소액의 분비 및 흡수와 관련된 미세구조의 변화를 알아보고자, 생후 10, 20, 35 그리고 80일 된 생쥐에서 부정소 상피세포를 전자현미경으로 관찰하였다. 생쥐 부정소의 분화과정은 미세구조의 특징에 따라 생후 20일가지의 미분화기, 생후 35일 전후의 성장 및 분화기, 그리고 성체의 성숙기로 구분되었다. 각 시기는 정소에서 세정관의 강소 형성시기 그리고 정소액과 더불어 정자가 부정소에 유입되는 시기와 밀접한 관계가 있었다. 성체의 부정소 상피세포 중 주세포는 두부 부정소 기부에서 흡수 기능을 갖는 구조였고, 두부의 말부와 체부 그리고 미부에서는 조면소포체와 골지체가 발달되어 단백질 합성과 분비가 왕성한 구조로 관찰되었다. 투명세포는 주로 체부와 미부에 존재하였으며 세포질내에 흡수과립이 많이 존재하였고, 그 속에는 정자에서 분리된 세포질 잔기로 사료되는 막구조물이 관찰되었다. 부정소 부위에 따라 상피세포의 종류와 분포가 달랐고, 동일한 종류이 상피세포라도 부위별로 미세구조가 다르게 관찰되었다.