• Korean Journal of Animal Reproduction
• /
• v.22 no.1
• /
• pp.29-34
• /
• 1998

Jugular plasma concentrations of luteinizing hormone, prolactin, estradiol-17\ulcorner and 13, 14-dihydro-15-keto-prostaglandin-F2봬(PGFM) were meausred prepartum during the last 12 days of pregnancy, at parturition, then 1 day after parturition in 16 goats. Plasma samples were analyzed for luteinizing hormone(LH), estradiol-17\ulcorner(E2), prolactin(PRL) and prostagladin F2봬(PGF2봬) concentrations by radioimmunoassay. 1. The concentrations of plasma luteinizing hormone in Korean native goats remained fairly constant(0.20 0.02\ulcorner0.38 0.04 mlu/ml) from 12 days prepartum to 1 postpartum but the concentrations of plasma prolactin rose slightly from 1 day prepartum. 2. The estradiol-17\ulcorner concentrations increased rapidly after day 1 before partum, reaching a peak at parturition(74.8 77.5 pg/ml), and falling to 63.8 2.8 pg/ml at day 1 postpartum. 3. Starting at 323.2 69.6 twelve days before parturition, the concentrations of plasma prostaglandin F2봬 rose during the 1 day preceeding parturition(650.7봬57.8 pg/ml) and peaked at 1081.4 164.9 on the day of parturition. At day 1 postpartum, the concentrations of PGF2봬 decreased to 425.3 60.4 pg/ml. Finally, these results show that changes in prostaglandin F2봬 concentrations before parturition were closely related to changes in estradiol-17\ulcorner concnetrations, but after parturition they remained elevated whereas estradiol-17\ulcorner concentrations fell abruptly.

• Korean Journal of Animal Reproduction
• /
• v.16 no.4
• /
• pp.325-333
• /
• 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
• /
• 2001.05a
• /
• pp.131-131
• /
• 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)

• Environmental Analysis Health and Toxicology
• /
• v.16 no.1
• /
• pp.21-28
• /
• 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 Animal Reproduction
• /
• v.8 no.2
• /
• pp.100-109
• /
• 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).

• Analytical Science and Technology
• /
• v.30 no.5
• /
• pp.226-233
• /
• 2017

In general, quantitative chemical analysis in various areas including food, the environment, in vitro diagnostics, etc., requires traceability in order to increase the reliability of the measurements. Measurement traceability is a property of an unbroken chain of comparisons relating an instrument's measurements to SI units. Purity analysis is the first process for establishing traceability to SI units in chemical measurements. The purpose of this study is to develop and validate a method of purity assignment for establishing the traceability of $17{\beta}$-estradiol measurements in an in vitro diagnostics field. The establishment of this method is very important as it can be applied to the development of CRM and to the analysis of the purity of other hormones. The method of assignment of the purity of $17{\beta}$-estradiol was developed using the mass balance method and was validated through participation in an International comparison. In the mass balance method, impurities are categorized into four classes as follows: total related structure impurities, water, residual organic solvents, and nonvolatiles/inorganics. In this study, total related structure impurities were characterized by a gas chromatography-flame ionization detector (GC-FID) and a high-performance liquid chromatography-ultraviolet (HPLC-UV) detector, water content was determined by a Karl-Fisher coulometer, and total residual solvents and nonvolatiles/inorganics were checked simultaneously by thermogravimetric analysis (TGA). The purity of the $17{\beta}$-estradiol was 985.6 mg/g and the expanded uncertainty was 2.1 mg/g at 95% confidence. The developed method can be applied to the development of certified reference materials, which play a critical role in traceability.

• The Korean Journal of Zoology
• /
• v.37 no.3
• /
• pp.377-384
• /
• 1994

The present study examines the inhibitow effect of progesterone (P) on luteinizing hormone $(LH)\beta$ subunit gene expression in anterior pituitary of ovariectomized, estradiol-treated adult rats. A single injection of P (1mg) further decreased the estradiol-Induced decrease in $LH\beta$ mRNA levels in ovariectomTzed rats in a time-dependent manner. p suppressed UIP mRNA levels at lower doses (0.1 and 1mg), but increased $LH\beta$ mRNA levels 81 a high dose (toms). The inhibitor action of P on $Uf\beta$ mRNA was restored when Ru486, a P receptor antagonist, was administered 1h before P treatment. These data clearly indicate that P inhibits gene expression of $LH\beta$ in the rift pituitary in a swersic manner with estrogen.

• The Plant Pathology Journal
• /
• v.27 no.4
• /
• pp.349-353
• /
• 2011

The ascomycete fungus Fusarium graminearum is an important plant pathogen responsible for Fusarium head blight in small grains and ear rot on maize. This fungus also produces the estrogenic metabolite, zearalenone (ZEA) that causes estrogenic disorders in humans and animals. Previously, we developed a conditional gene expression system for this fungus using a ZEA-inducible promoter (Pzear). In the present study, four other estrogenic compounds, including ${\beta}$-estradiol, estriol, estrone, and secoisolariciresinol, were screened as possible substitutes for ZEA in this system. Among them, ${\beta}$-estradiol was able to successfully induce the expression of a gene controlled by Pzear, while estrone was only able to partially induce its expression but the other two compounds were not effective. In combination, these results demonstrate that ${\beta}$-estradiol can replace ZEA in this conditional gene expression system, thereby eliminating the need to use the more expensive reagent, ZEA, and facilitating high-throughput functional analyses of F. graminearum in future studies.

• Environmental Mutagens and Carcinogens
• /
• v.22 no.4
• /
• pp.274-278
• /
• 2002

Phthalates, suspected endocrine disruptor, are plasticizer and solvent used in industry, and some phthalates are known as potential carcinogen. Most common human exposure to this compounds may occur with contaminated food. It may migrate into food from plastic wrap or may enter food from general environmental contamination, and it has become widespread environmental pollutants, thus leading to a variety of phthalates that possibly threaten the public health. Dibutyl phthalate (DBP) may playa part of cell proliferator, which mediates changes in gene expression and the metabolism of xenobiotics. An understanding of the role of DBP in modulating gene regulation should provide insight regarding mechanisms of DBP induced xenoestrogenic impact. To elucidate the type of genes that are associated with estrogenic activity induced by DBP at the dose (10$^{-8}$ M) appeared proliferating effects, the pattern of gene expression in MCF7 cells was compared between 17$\beta$-estradiol and DBP exposure in the cDNA microarray. From the results, it showed some differences of gene expression patterns between MCF7 cells treated with 17$\beta$-estradiol and DBP, and also DBP shows estrogenic potential with changes in estrogen-related gene expression levels.

• Asian Pacific Journal of Cancer Prevention
• /
• v.16 no.6
• /
• pp.2161-2166
• /
• 2015

Estrogen receptors (ERs) are steroid receptors located in the cytoplasm and on the nuclear membrane. The sequence similarities of human $ER{\alpha}$, mouse $ER{\alpha}$, rat $ER{\alpha}$, dog $ER{\alpha}$, and cat $ER{\alpha}$ are above 90%, but structures of $ER{\alpha}$ may different among species. Estrogen can be agonist and antagonist depending on its target organs. This hormone play roles in several diseases including breast cancer. There are variety of the relative binding affinity (RBA) of ER and estrogen species in comparison to $17{\beta}-estradiol$ (E2), which is a natural ligand of both $ER{\alpha}$ and $ER{\beta}$. The RBA of the estrogen species are as following: diethyl stilbestrol (DES) > hexestrol > dienestrol > $17{\beta}-estradiol$ (E2) > 17- estradiol > moxestrol > estriol (E3) >4-OH estradiol > estrone-3-sulfate. Estrogen mimetic drugs, selective estrogen receptor modulators (SERMs), have been used as hormonal therapy for ER positive breast cancer and postmenopausal osteoporosis. In the postgenomic era, in silico models have become effective tools for modern drug discovery. These provide three dimensional structures of many transmembrane receptors and enzymes, which are important targets of de novo drug development. The estimated inhibition constants (Ki) from computational model have been used as a screening procedure before in vitro and in vivo studies.