• Korean Journal of Animal Reproduction
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• v.16 no.4
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• pp.325-333
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• 1993

A competitive type immunoassay method for 17$\beta$-estradiol(E2) based on the idiotypic anti-idiotypic antibody and time-resolved fluorescence is described. The anti-idiotypic antibody(Ab2) produced to E2 binding site of the primary idiotype antibody (Ab1) was labelled with europium and was allowed to compete with E2 standards or serum sample for the binding sites of Ab1 which was bound to 2nd antibody captured ontothe surface of microtitre plates. Fluorescence measured by time-resolved fluorometer was inversely proportional to the concentration of E2 over the range 5~500pg/well. The sensitivity of the assay was 5pg per well which was compatible with that ofradioimmunoassay using the same Ab1 and 3H-E2 as a tracer. One great advantage of this method described here was to enable antibodies to be labelled instead of haptens, and thus makes it easier to develop sensitive and robust immunoassay systems specially for haptens.

• Proceedings of the Korea Society of Environmental Toocicology Conference
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• 2001.05a
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• pp.131-131
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• 2001

내분비계장애물질에 대한 검색기법의 하나로 수컷 어류의 교배행위 및 생식력에 대한 in vivo 연구를 시도하였다. 수컷 송사리(Oryzias latipes)에 대표적 에스트로젠인 17$\beta$-estradiol를 2 및 20 $\mu\textrm{g}$/L의 농도로 각 노출군당 5마리씩 14일간 노출시킨 후 각 군당 임의로 2마리씩 선택하여 Prostaglandin F2$\alpha$를 주사한 3마리의 정상 암컷 송사리와의 교배행위를 비디오 카메라를 이용하여 1시간 동안 녹화하여 분석하였다. (중략)

• The Journal of Korean Medicine
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• v.22 no.4
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• pp.22-28
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• 2001

흰쥐의 난소 절제로 야기된 골손실에 미치는 골쇄보의 영향을 관찰하였다. 난소 절제 후 흰쥐의 체중은 증가하고 자궁의 무게는 감소하였는데, 골쇄보는 특별한 영향을 주지 않았다. 그러나, 난소 절제 후 흰쥐의 tibia에서 측정한 골밀도는 대조군에 비하여 22% 감소되었으나, 골쇄보와 17be1a-estradiol를 투여한 경우는 골밀도의 감소가 현저히 억제되었다. 난소를 절제한 실험군에 골쇄보와 17be1a-estradiol를 투여하고 전자 현미경으로 관찰한 결과, trabecular bone의 미세분자 표면이 보호되는 것으로 관찰되었다. 이러한 결과들을 볼 때, 골쇄보가 17be1a-estradiol 만큼 난소 절제술 후 진행되는 골손실을 예방하는데 효과적임을 강하게 나타내고 있다고 사료된다.

• Environmental Analysis Health and Toxicology
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• v.16 no.1
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• pp.21-28
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• 2001

A common used endpoint in bioassays testing the estrogenicity of chemicals including endocrine disruptors is the induction of egg yolk Precursor vitellogenin in male fish. Two marine fishes (Sebastes schlegeli and Paralichthys olivaceus) were exposed to the 17$\beta$-estradiol(E2) to determine the vitellogenin production. Vitellogenin was measured in fish blood using SDS-PAGE and Densimetry. Results showed that exposure to E2 caused vitellogenin in male fish. Especially, vitellogenin levels in young fish were about 4 times higher than in adult fish, which means young fish are more sensitive to E2 exposure. And plasma vitellogenin in fish increased related to E2 concentration and exposure duration.

• Korean Journal of Agricultural Science
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• v.17 no.1
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• pp.34-44
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• 1990

The study was carried out to elucidate the effects of ovarian function on the thyroid gland, adrenal gland and uterus in female rats. One hundred and forty-four mature female rats were allotted into the three groups ; ovariectomized group, estradiol treated group and intact control group. The ovaries of 48 heads of rats were completely removed. Forty eight heads of rats were administered with $200{\mu}g$ of estradiol benzoate every 48 hours. Serum estradiol-$17{\beta}$ and progesterone levels were determined with radioimmunoassay method at 3, 6, 12, 24 hours and 5, 10, 15 days after treatment. The rats were necropsied to measure weights of thyroid gland, adrenal gland and uterus and to examine the histological changes in the organs. The results obtained were as follows ; 1. Serum estradiol-$17{\beta}$ levels were rapidly decreased below 27.20pg/ml 18 hours after ovariectomy. In estradiol treated rats the levels were rapidly increased 18 hours after treatment, but thereafter slowly decreased. The significant differences in the estradiol level were found between the group at every observation time. 2. Serum progesterone levels were significantly decreased after ovariectomy and estradiol injection. The lowest level was found in the group of ovariectomized rats. 3. The weights of thyroid glands decreased in ovariectomized rats rather than in intact rats 5 days after treatment. The weights tended to increase after estradiol injection but significant differences between the groups were seen on 10th and 15th days. 4. In the histological findings of thyroid glands, follicular epithelial cells were changed to be squamous 5 days after ovariectomy and accompanied pyknosis 10 days and karyorrhexis 15 days after ovariectomy. On the contrary follicular epithelial cells were changed to be columnar with hypertrophy 10 days after estradiol injection. 5. The significant differences in adrenal gland weights were recognized between all the groups 5 and 15 days after treatment in ovariectomized rats were lighter than intact rats and the adrenal gland weights were rather heavier in estradiol treated rats. 6. The days after ovariectomy the adrenal glands were atrophied accompanying with pyknosis in the cortical cells of zona fasciculata. The cells in zona fasciculata and zona reticularis started to hypertrophy 5 days after estradiol injection, but no changes were found in the zona glomerulosa of adrenal cortex and in the adrenal medulla. 7. The significant differences in uterus weights were recognized between the groups at each observation time. After ovariectomy the uterus weights decreased rapidly but after estradiol injection they increased rapidly. 8. Through histological examination of uterus, the atrophy and degeneration started to occur in endometrium and lamina propria 12 hours after ovariectomy, and in myometrium one day after ovariectomy, and the changes progressed rapidly after that. On the contrary, the myometrium was proliferated and hypertrophied from 12 hours after estradiol-$17{\beta}$ injection.

• Korean Journal of Animal Reproduction
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• v.8 no.2
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• pp.100-109
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• 1984

This study was conducted to find out the changes of progesterone and estradiol-17$\beta$ levels in the serum of female Korean native goats during the reproductive stages such as the estrous cycle, pregnancy and periparturient period. Nine heads of female Korean native goats of 3 year old in average and weighing 35.7$\pm$1.4 kg were offered for the experiment. Blood samples were taken at 0, 1, 2, 5, 7, 10, 13, 15, 18 and 19 days after onset of estrus, and 1, 30, 60, 90, 120 and 149 days of pregnancy, and -5, -2, -1, 0, +1, +2 and +5 days of periparturient period where minus figures denote the days before paturition. The progesterone, estradiol-17$\beta$ in the serum samples were assayed by radioimmunoassay methods. The results of this study are summarized as follow: 1. The progesterone levels during the estrous cycles reached a peak level of 0.98$\pm$0.60ng/ml at 13 days after onset of estrus and decreased thereafter and were lower than 0.09$\pm$0.02mg/ml on the first day of estrus. 2. The estradioe17$\beta$ levels during the estrous cycles showed a peak level of 15.97$\pm$1.72pg/ml at onest of estrus, and decreased (5.41$\pm$0.51pg/ml-9.09$\pm$1.82pg/ml) during luteal phase. 3. The progesterone levels during the gestation period increased from day 1 and peaked at 90 days after mating and then decreased until 149 days. The peak level was 6.27$\pm$0.23ng/ml at 90 days. 4. The estradiol-17$\beta$ levels during the gestation period showed gradual increase, which were 9.03$\pm$0.88, 32.96$\pm$2.85, 46.03$\pm$2.42, and 54.06$\pm$1.64pg/ml on 30, 60, 90 and 120 dyas after mating respectively. 5. The progesterone levels measured from 5 days before the parturition to 5 days after showed the highest level at the shart of measurement (4.46$\pm$0.31ng/ml) and decreased gradually and bottomed out at one day post-partum and thereafter (0.24$\pm$0.02-0.45$\pm$0.06ng/ml). 6. The estradiol-17$\beta$ levels measured during the same periparturient period as progesterone showed increase to reach the peak level at 1 day before parturition and decreased rapidly thereafter (-5 dyas 69.46$\pm$3.62, -2 days 107.07$\pm$1.91, -1 days 137.83$\pm$7.54, 0 days 50.06$\pm$6.71 and +1 to +5 days 3.21-4.72 pg/ml).

• Korean Journal of Animal Reproduction
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• v.19 no.2
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• pp.119-127
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• 1995

These studies were carried out to examine the estradiol-17$\beta$ levelsin plasma and ovarian tissues, as well as the contents of collagen and catecholamines in the uterus, and to determine the effects of GnRH administrations of uterine involution in postpartum Korean native goats. Plasma concentrations of estradiol-17$\beta$ were 63.81$\pm$8.00 pg/ml at day 1 of kidding, declined to 36.78$\pm$22.90 ng/ml at day 24 and decreased progressively to 27.81$\pm$17.06 and 12.46$\pm$8.13 pg/ml at days 30 and 36 postpartum, respectively. In ovarian tissues, the concentrations of estaiol-17$\beta$ were increased just before parturition and decreased immediately after parturition. The plasma estradiol-17$\beta$ levels were slightly higher on days 12 and then decreased gradually after parturition. The concentraitons of estradiol-17$\beta$ in the ovaries of postpartum goats were increased at day 36 after treatments with GnRH. The total hydroxyproline contents in the uterus was slightly higher prior to parturition and decreased gradually with the postpartum intervals after parturition. Hydroxyproline concentraitons in the uterus were decreased at days 24 and 36 postpartum after treatments with GnRH. The norepinephrine concentrations in myometrium from the pregnant and postpartum goats were correspondingly low both immediately before and after partuition. Norepinephrine concentrations in the pregnant horn of the uterus were increased from days 12 to 36 of postpartum and those levels of the non-pregnant horn were also increased from days 24 to 36 postpartum. Slightly higher concentrations were present in the non-pregnant horn in comparison to the pregnant horn but these differences were not significant. Postpartum, the uterine norepinephrine concentration was slightly increased at day 36 after treatments with GnRH. Dopamine concentrations were greater than those of norepinephrine. The concentrations of dopamine in the uterus of pregnant goats was not significantly different from that in the postpartum animals. Dopamine concentraitons of pregnant horn in postpartum goats were increased at day 24 after treatments with GnRH.

• Archives of Pharmacal Research
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• v.17 no.2
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• pp.109-114
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• 1994

The role of sex homones in hepatic lipid peroxidation, and in hepatic adehyde odidase and xanthine oxidase activites were investigated using rat liver homogenates. It was observed that male rt had a significantly greater content of malondialdehyde in liver than female. Among the sex hormones tested, estradiol, one of female hormones, markedly inhibited the formation of lipid peroxides in liver tissues in vitro. Especially, the inhibitory effect of estradiol appeared more remarkably in Fe-induced lipid peroxidation. The hepatic xanthine oxidase activity was decreased about 15% by $10\;^6\;M$ estradiol, wherease, the adehyde oxidase activity was almost completely disappeared at the same concentration of estradiol. It implies that sex differences in lipid peroxidation is attributed to the suppression of radical generating system by estradiol.

• Korean Journal of Animal Reproduction
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• v.26 no.2
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• pp.183-192
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• 2002

The present studies were carried out to examine the effects of exogenous oxytocin(OT) on plasma, uterine and placenta of estradiol-17$\beta$, progesterone, prostaglandin F$_2$$_{\alpha}$ (PGF$_2$$_{\alpha}$), Prostaglandin E$_2$(PGE$_2$) and OT receptor concentrations in pregnant rats. Pregnant rats received an injection of exogenous OT on days 14, 16, 18, 20, 22 of pregnancy and day 1 of postpartum. Concentrations of plasma estradiol-17 $\beta$ after OT injection started to increase after day 18 and peaked on day 22 of pregnancy but decreased on day 1 of postpartum. Plasma progesterone concentrations declined gradually from day 18 of pregnancy and decreased more rapidly until postpartum 1 day. Concentrations of estradiol-17$\beta$in uterine tissues after OT injection were sharply increased from day 20 to 22 of pregnancy and progestrone concentrations were peaked on day 16 and decreased rapidly from day 16 to 20 and maintained the same level until day 1 of postpartum. Uterine concentrations of PGF$_2$$_{\alpha}$ and PGE$_2$increased gradually until day 20 and peaked on day 22 of pregnancy but showed a marked decrease on day 1 of postpartum. Concentrations of PGF$_2$$_{\alpha}$ in placental tissues increased rapidly from day 14 of pregnancy and decreased sharply on day 1 of postpartum. Concentrations of PGE$_2$increased gradually after day 14 and peaked on day 20 of pregnancy. The concentration of OT receptor in uterus was significantly elevated from day 20 and rose to maximum on day 22 of pregnancy. These findings show that OT suppress the concentration of progestrone and stimulate productions of estradiol-17 $\beta$, PGF$_2$$_{\alpha}$, PGE$_2$ and oxytocin receptor concentrations in pregnant rats.

• Journal of Gastric Cancer
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• v.13 no.3
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• pp.172-178
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• 2013

Purpose: The aims of this study were as follow: 1) to de scribe the expression status of estrogen receptor-${\alpha}$ and -${\beta}$ mRNAs in five gastric carcinoma cell lines; 2) to evaluate in vitro the effects of $17{\beta}$-estradiol and estrogen receptor antagonists on the proliferation of the cell lines. Materials and Methods: Detection of estrogen receptor-${\alpha}$ and estrogen receptor-${\beta}$ mRNA in five human gastric cancer cell lines (AGS, KATO III, MKN28, MKN45 and MKN74) was made by the reverse transcription-polymerase chain reaction system. To evaluate the effect of $17{\beta}$-estradiol and estrogen receptor antagonists on the proliferation of gastric cancer cell line, the cell lines which expressed both es trogen receptors were chosen and treated with $17{\beta}$-estradiol and estrogen receptor antagonists (methyl-piperidino-pyrazole and pyrazolo [1,5-a] pyrimidine). Cell proliferation was assessed with the methylthiazol tetrazolium test. Results: Estrogen receptor-${\alpha}$ and estrogen receptor-${\beta}$ mRNAs were expressed in three (KATO III, MKN28 and MKN45) and all of the five gastric cancer cell lines, respectively. At higher concentrations, $17{\beta}$-estradiol inhibited cell growth of MKN28, MKN45 and KATO III cell lines. Neither estrogen receptor-${\alpha}$ nor estrogen receptor-${\beta}$ antagonist blocked the anti-proliferative effect of $17{\beta}$-estradiol. Conclusions: Our results indicate that estrogen receptor-${\beta}$ mRNAs are preferentially expressed in gastric cancers and also imply that hormone therapy rather than estrogen receptor blockers may be a useful strategy for the treatment of estrogen receptor-${\beta}$ positive gastric cancer. Its therapeutic significance in gastric cancer are, however, limited until more evidence of the roles of estrogen receptors in the gastric cancer are accumulated.