3.Prostaglandin E2 and F2?concentrations in human oviductal tissue during different phases of the menstrual cycle.
In Sook SOHN ; Chan Ho SONG ; Ki Hyun PARK ; Young Ja PARK ; Kyung Ja YU
Korean Journal of Obstetrics and Gynecology 1993;36(7):2262-2269
No abstract available.
Animals
;
Dinoprostone*
;
Female
;
Humans*
;
Menstrual Cycle*
;
Oviducts*
4.Studies on the lectin binding patterns of the oviduct luminal epithelium and oocytes in mouse.
Myung Chan GYE ; Sung Rye KIM ; Hae Kwon KIM ; Moon Kyoo KIM
Korean Journal of Fertility and Sterility 1993;20(3):267-276
No abstract available.
Animals
;
Epithelium*
;
Mice*
;
Oocytes*
;
Oviducts*
;
Phenobarbital*
5.A Morphometric Study on the Changes in the Size of Human Oviduct and Ovary after Immersion in Formalin.
Tae Sun WHANG ; Ho Suck KANG ; Byung Pil CHO
Korean Journal of Physical Anthropology 1994;7(2):157-162
The changes in the size of human oviduct and ovary after immersion in formalin (4%, 10%) were investigated. The results were as follows : 1. After fixation, the length of oviduct was significantly reduced to 93%, but the cross sectional area of oviduct was significantly increased. The length of oviduct showed no significant difference between 4% and 10% formalin. The length of ovarian ligament was also significantly reduced to 84% after fixation. 2. After fixation, the volume of oviduct was increased significantly and showed a difference between the two fixatives. The volume of oviduct in 4% formalin has increased to 107%, as compared to 103% increase in 10% formalin. 3. After fixation, the volume of ovary was increased significantly and showed a difference between the two fixatives. The volume of ovary in 4% formalin has increased to 109%, as compared to 103% increase in 10% formalin.
Animals
;
Female
;
Fixatives
;
Formaldehyde*
;
Humans*
;
Immersion*
;
Ligaments
;
Ovary*
;
Oviducts*
6.A study on the activity of alkaline phosphatase of rat oviduct during early embryonic development.
Korean Journal of Fertility and Sterility 1991;18(1):41-48
No abstract available.
Alkaline Phosphatase*
;
Animals
;
Embryonic Development*
;
Female
;
Oviducts*
;
Pregnancy
;
Rats*
7.Torsion of The Follopian Tube in an Adolescent Female.
Young Hye KIM ; Min Chang KANG ; Hyuk JUNG
Korean Journal of Obstetrics and Gynecology 2004;47(7):1447-1449
Torsion of the follopian tube is an infrequent but significant cause of acute lower abdominal pain in females that is difficult to recognize preoperatively, although prompt diagnosis and timely sugical treatment are vital to salvage the oviduct. Unless a high index of suspicion is maintained for torsion of the fallopian tube in a adolescent females, this disorder may not be detected until after tubal destruction.
Abdominal Pain
;
Adolescent*
;
Animals
;
Diagnosis
;
Fallopian Tubes
;
Female*
;
Humans
;
Oviducts
8.Effect of Partial Laser Assisted Hatching on Mouse Embryos.
Dong Hoon KIM ; Myo Kyung KIM ; Hoi Chang LEE ; Duck Sung KO ; Won Il PARK ; Hyuck Chan KWON ; Ho Joon LEE
Korean Journal of Fertility and Sterility 2001;28(2):147-154
OBJECTIVE: The present study was performed to investigate the efficiency of partial laser assisted hatching (p-LAH; lased 1/2 ZP width from ZP edge) on hatching of mouse blastocysts. METHODS: We used non-contact 1.48 micrometer diode laser (MTM, Switzland) to create a precise hole on zona pellucida. 2-cell embryos were collected from the mouse (ICR) oviduct at 48 hours after hCG administration. Collected 2-cell embryos were cultured in the P-1 medium supplemented with 0.4% BSA. For experiments, embryos at 8-cell stage were used after 20~22 hours in culture. After conventional (c-LAH) or partial laser assisted hatching, the embryos were further cultured in P-1 medium supplemented with 0.4% BSA for 3 days. To compare efficiency of complete and partial laser assisted hatching, hatching rate, hatching time and blastocyst diameter and zona pellucida thickness at hatching time were investigated. Embryos were examined every 12 hours. Blastocyst diameter and zona pellucida thickness at hatching time were measured with an ocular micrometer. RESULTS: Hatching rates of p-LAH group (84.2%) was significantly higher than that of control group (39.3%), but there was no difference between the p-LAH (84.2%) and c-LAH (91.2%). p-LAH group was hatched 12 hours earlier than control group, but hatched 12 hours later than c-LAH group. The diameter of blastocyst at hatching time of p-LAH group (113.1+/-6.4 micrometer) was smaller than that of control group (122.2+/-5.0 micrometer), but larger than that of c-LAH group (102.2+/-2.7 micrometer). Zona pellucida thickness at hatching time of p-LAH group (6.4+/-0.9 micrometer) was thicker than that of control group (4.5+/-1.5 micrometer), but thinner than that of c-LAH group (10.0+/-0.8 micrometer). CONCLUSION: These results suggest that p-LAH may maintains the cell arrangement of early embryos to ensure successful development and prevent precocious hatching of blastocyst when compare to c-LAH and conventional (acidic tyrode) AH. Thus, p-LAH may provide a valuable and effective AH technique for human ART program.
Animals
;
Blastocyst
;
Embryonic Structures*
;
Humans
;
Lasers, Semiconductor
;
Mice*
;
Oviducts
;
Zona Pellucida
9.Isolated torsion of fallopian tube during pregnancy treated with laparoscopic operation; A case report.
Hee Sun IM ; Sae Hyun PARK ; Jae Dong LEE ; Jong Ok KIM ; Eun Kyung PARK ; Yong Seok LEE ; Hae Nam LEE
Korean Journal of Obstetrics and Gynecology 2007;50(12):1757-1761
Isolated torsion of the fallopian tube is very uncommon during pregnancy. It usually confuses with acute appendicitis and torsion of the ovary. The diagnosis is usually established during operation, and a salpingectomy is almost always necessary. However, the early diagnosis and surgical treatment of the disease are mandatory to preserve oviduct. Because of safety and feasibility, laparoscopic surgery has recently become major treatment method.
Animals
;
Appendicitis
;
Diagnosis
;
Early Diagnosis
;
Fallopian Tubes*
;
Female
;
Laparoscopy
;
Ovary
;
Oviducts
;
Pregnancy*
;
Salpingectomy
10.Effect of Magnesium Ion in the Culture Medium on the Development of Preimplantation Mouse Embryos In Vitro.
Soo Jin CHOI ; Jin Hyun JUN ; Yong Seog PARK ; In Ha BAE
Korean Journal of Fertility and Sterility 2001;28(3):199-208
OBJECTIVE: The present study was undertaken to examine the effects of magnesium ion in the culture medium on the development of mouse fertilized oocytes either before or after pronuclear formation, and to investigate whether the effect of magnesium ion is related with the redistributional change of mitochondria. METHODS: Fertilized oocytes obtained from the oviducts of mice at 15 hr after hCG injection before pronuclear formation (pre-PN) or 21 hr after hCG injection after pronuclear formation (post-PN) were used. The embryos were cultured for 3 days with basic T6 medium-magnesium free and various concentrations of magnesium ion, 0.0, 0.5, 1.0, 2.0, 4.0 or 8.0 mM, respectively. After culture, the developmental stages of embryos and the number of nuclei were evaluated. To observe the effects of magnesium ion on the mitochondrial distribution, fertilized oocytes were collected at 21 hr after hCG injection and cultured for 6 hr with various concentration of magnesium ion. As a control, fertilized oocytes with pronuclei at 27 hr after hCG injection were used. RESULTS: The concentration of magnesium ion to accelerate the in vitro development of mouse fertilized oocytes appeared to be at 2.0 mM for the pre-PN and the post-PN stage embryos. In the mitochondrial redistribution patterns, the embryos cultured in 2.0 mM concentration of magnesium ion showed the highest percentage (22.6%) of distinct perinuclear clustering pattern comparing to other experimental group. CONCLUSION: The effect of magnesium ion may be related to the cytoplasmic redistribution of mitochondria. This relationship seems to connect the developmental competence of preimplantation mouse embryos in vitro. These results can suggest that higher concentration of magnesium ion (2.0 mM) than those of conventional culture medium (0.2~1.2 mM) is more suitable for in vitro culture of preimplantation mouse embryos.
Animals
;
Cytoplasm
;
Embryonic Structures*
;
Magnesium*
;
Mental Competency
;
Mice*
;
Mitochondria
;
Oocytes
;
Oviducts