• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제30권4호
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• pp.323-330
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• 2004

Estrogen may promote osteoblast/osteocyte viability by limiting apoptotic cell death. We hypothesize that hsp27 is an estrogen- regulated protein that can promote osteoblast viability by increasing osteoblast resistance to apoptosis. The purpose of this study was to determine the effect of estrogen treatment and heat shock on $TNF{\alpha}$ - induced apoptosis in the MC3T3-E1 cell line. Cells were treated with 0 - 100 nM $17{\beta}$ estradiol (or ICI 182780) for 0 - 24 hours before heat shock. After recovery, apoptosis was induced by treatment with 0 - 10 ng/ml TNF${\alpha}$. Hsp levels were evaluated by Northern and Western analysis using hsp27, hsp47, hsp70c and hsp70i - specific reagents. Apoptosis was revealed by in situ labeling with Terminal Deoxyribonucleotide Transferase (TUNEL). A 5 - fold increase in hsp27 protein and mRNA was noted after 5 hours of treatment with 10 - 20 nM $17{\beta}$ estradiol prior to heat shock. Increased abundance of hsp47, hsp70c or hsp70i was not observed. TUNEL indicated that estrogen treatment also reduced (50%) MC3T3-E1 cell susceptibility to $TNF{\alpha}$ - induced apoptosis. Treatment with hsp27-specific antisense oligonucleotides prevented hsp27 protein expression and abolished the protective effects of heat shock and estrogen treatment on $TNF{\alpha}$- induced apoptosis. Hsp27 is a determinant of osteoblast apoptosis, and estrogen treatment increases hsp27 levels in cultured osteoblastic cells. Hsp27 contributes to the control of osteoblast apoptosis and may be manipulated by estrogenic or alternative pathways for the improvement of bone mass.

• Toxicological Research
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• 제20권3호
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• pp.205-211
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• 2004

Concern that some chemicals in our environment may affect human health by disrupt-ing normal endocrine function has prompted a research on interactions of environmental contaminants with steroid hormone receptor. Toxaphene and chlordane are among the 12 persistent organic pollutants identified by the United Nations Environment Programme as requiring urgent attention. We compared the estrogenic activity of two organochlorine pesticides, toxaphene and chlordane, at estrogen receptor a (ER$\alpha$) and estrogen receptor $\beta$ (ER$\beta$). Human hepatoma cells (HepG2) were transiently transfected with rat ER$\alpha$ or ER$\beta$ plus an estrogen-responsive complement C3-luciferase (C3-Luc) reporter gene. After transfection, cells were treated with various concentrations of toxaphene and chlordane to investigate agonism or antagonism of these chemicals. Both toxaphene and chlordane were potent agonists in HepG2 cells for ER$\alpha$. In contrast, these chemicals had a minimal agonist activity with ER$\beta$ and almost abolished 17$\beta$-estradiol-induced ER$\beta$-mediated activity. Therefore, toxaphene and chlordane behaved as an ER$\alpha$ agonist and an ER$\beta$ antagonist with estrogen-responsive reporter plasmid C3-Luc, and exposure to these organochlorine pesticides could have a crictical effect on normal endocrine function.

• Asian Pacific Journal of Cancer Prevention
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• 제17권4호
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• pp.1851-1855
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• 2016

Tamoxifen is a pharmacological estrogen inhibitor that binds to the estrogen receptor (ER) in breast cells. However, it shows an estrogenic effect in other organs, which causes adverse drug reactions (ADRs). The sulfotransferase 1A1 (SULT1A1) enzyme encoded by the SULT1A1 gene is involved in estrogen metabolism. Previous research has suggested that the SULT1A1 copy number is linked with the plasma estradiol (E2) concentration. Here, a total of 34 premenopausal breast cancer patients, selected from the Thai Tamoxifen (TTAM) Project, were screened for their SULT1A1 copy number, plasma E2 concentration and ADRs. The mean age was $44.3{\pm}11.1years$, and they were subtyped as ER+/progesterone receptor (PR)+ (28 patients), ER+/PR- (5 patients) and ER-/PR- (1 patient). Three patients reported ADRs, which were irregular menstruation (2 patients) and vaginal discharge (1 patient). Most (33) patients had two SULT1A1 copies, with one patient having three copies. The median plasma E2 concentration was 1,575.6 (IQR 865.4) pg/ml. Patients with ADRs had significantly higher plasma E2 concentrations than those patients without ADRs (p = 0.014). The plasma E2 concentration was numerically higher in the patient with three SULT1A1 copies, but this lacked statistical significance.

• Bulletin of the Korean Chemical Society
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• 제34권4호
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• pp.1131-1136
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• 2013

Parabens, the esters of p-hydroxybenzoic acid, have been widely used as antimicrobial preservatives in cosmetic products, drugs, and processed foods and beverages. However, some parabens have been shown to have weak estrogenic effects through in vivo and in vitro studies. Because such widespread use has raised concerns about the potential human health risks associated with exposure to parabens, we developed a simultaneous analytical method to quantify 4 parabens (methyl, ethyl, propyl, and butyl) in human urine, by using solid-phase extraction and high-performance liquid chromatography coupled with triple quadrupole mass spectrometry. This method showed good specificity, linearity ($R^2$ > 0.999), accuracy (92.2-112.4%), precision (0.9-9.6%, CV), and recovery (95.7-102.0%). The LOQs for the 4 parabens were 1.0, 0.5, 0.2, and 0.5 ng/mL, respectively. This method could be used for quick and accurate analysis of a large number of human samples in epidemiological studies to assess the prevalence of human exposure to parabens.

• Molecules and Cells
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• 제26권1호
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• pp.74-80
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• 2008

Bisphenol A bis (2,3-dihydroxypropyl) ether ($BADGE.2H_2O$) is a component of commercial liquid epoxy resins commonly used in the food-packing industry and in dental sealants. There is evidence that it has significant estrogenic activity. Nur77 plays a crucial role in the regulation of certain genes involved in LH-mediated steroidogenesis in testicular Leydig cells. It was previously demonstrated that Bisphenol A (BPA) stimulates Nur77 gene induction and steroidogenesis. In this study, we investigated the effects of $BADGE.2H_2O$ on Nur77 gene expression and steroidogenesis. Northern blot analysis showed that it increased the expression of Nur77 mRNA and protein, and transient transfection assays demonstrated that it increased the promoter activity and transactivation of Nur77. It also increased the expression of certain steroidogenic genes, such as StAR and $3{\beta}$-HSD. Finally, over-expression of a dominant negative Nur77 cDNA via adenoviral infection reduced $BADGE.2H_2O$-mediated progesterone biosynthesis. These results indicate that $BADGE.2H_2O$ disrupts testicular steroidogenesis by increasing Nur77 gene expression.

• BMB Reports
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• 제38권3호
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• pp.300-306
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• 2005

Tamoxifen citrate is an anti-estrogenic drug used for the treatment of breast cancer. It showed a degree of hepatic carcinogenesis, when it used for long term as it can decrease the hexose monophosphate shunt and thereby increasing the incidence of oxidative stress in liver rat cells leading to liver injury. In this study, a model of liver injury in female rats was done by intraperitoneal injection of tamoxifen in a dose of 45 mg/kg body weight for 7 successive days. This model produced a state of oxidative stress accompanied with liver injury as noticed by significant declines in the antioxidant enzymes (glutathione-S-transferase, glutathione peroxidase and catalase) and reduced glutathione concomitant with significant elevations in TBARS (thiobarbituric acid reactive substance) and liver transaminases; sGPT (serum glutamate pyruvate transaminase) and sGOT (serum glutamate oxaloacetate transaminase) levels. The oral administration of dimethyl dimethoxy biphenyl dicarboxylate (DDB) in a dose of 200 mg/kg body weight daily for 10 successive days, resulted in alleviation of the oxidative stress status of tamoxifen-intoxicated liver injury in rats as observed by significant increments in the antioxidant enzymes (glutathione-S-transferase, glutathione peroxidase and catalase) and reduced glutathione concomitant with significant decrements in TBARS and liver transaminases; sGPT and sGOT levels. The administration of DDB before tamoxifen intoxication (as protection) is more little effective than its curative effect against tamoxifen-induced liver injury. The data obtained from this study speculated that DDB can mediate its biochemical effects through the enhancement of the antioxidant enzyme activities and reduced glutathione level as well as decreasing lipid peroxides.

• 대한한방부인과학회지
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• 제30권4호
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• pp.18-44
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• 2017

목 적: 이 연구에서는 한의학에서 다양한 부인과 질환에 사용되어온 전통 복합 처방인 귀비탕과 가미온담탕을 합방, 가감한 가감귀비온담탕 열수 추출물의 갱년기 장애 개선 효과를 심혈관 장애, 비만, 고지혈증, 골다공증, 장기 지방축적 및 신경정신 장애를 포함한 다양한 사람의 갱년기 장애를 나타내는 것으로 알려진 난소적출(Ovariectomized, OVX) 랫트 모델을 이용하여 평가하였다. 방 법: 난소적출수술 28일 후부터 가감귀비온담탕 추출물(수율 : 22.03%)을 각각 100, 50 및 25 mg/ml의 농도로 멸균 증류수에 용해시키고, 체중 kg 당 5 ml의 용량(500, 250 및 125 mg/kg)으로 매일 1회씩 84일(12주 : 3개월)간 경구 투여한 다음, 항비만효과, 항자궁위축효과 및 골다공증 억제 효과의 3가지 생리활성 효과로 구분하여 평가하였다. 항비만 효과 및 항자궁위축효과를 평가하기 위해, 체중 및 증체량, 혈청중 에스트라디올 함량, 복부 축적 지방 및 자궁의 중량의 변화와 복부 축적 지방의 두께 및 평균 지방세포 직경, 자궁 전체, 상피 및 점막의 두께와 점막내 자궁샘이 차지하는 비율의 변화를 각각 평가하였다. 또한 골다공증 개선효과, 즉 골 보호효과를 평가하기 위해, 대퇴골, 경골 및 요추골의 습, 건조 및 탄화 중량, 골밀도, 골강도, 혈중 osteocalcin 및 bone specific alkaline phosphatase(bALP) 함량, 골량 및 구조와 골흡수에 대한 조직병리학적 변화를 각각 측정하였다. 실험군(5개군; 군당 8마리의 랫트 사용) 거짓수술 대조군(거짓수술 후, 증류수 투여 대조군) 난소적출 대조군(난소적출 수술 후, 증류수 투여 대조군) GGOT500(난소적출 수술 후, 가감귀비온담탕 추출물 500 mg/kg 투여 고용량 실험군) GGOT250(난소적출 수술 후, 가감귀비온담탕 추출물 250 mg/kg 투여 중간용량 실험군) GGOT125(난소적출 수술 후, 가감귀비온담탕 추출물 125 mg/kg 투여 저용량 실험군) 결 과: 난소적출 대조군에서는 거짓수술 대조군에 비해 현저한 체중 및 증체량, 사료 및 물 섭취량, 축적 복부 지방 중량, 혈청 중 osteocalcin 함량의 증가가 자궁, 대퇴골, 경골 및 L5 중량과 혈중 bALP 및 에스트라디올 함량의 감소와 함께 인정되었으며, 현저한 복벽 축적 지방 두께의 증가 및 자궁의 위축, 대퇴골, 경골 및 L4의 골량 및 구조의 감소 소견이 골 흡수 지표(Ocn 및 OS/BS)의 현저한 증가와 함께 조직병리학적 및 조직형태계측학적으로 인정되었다. 즉, 전형적인 에스트로겐 결핍성 갱년기 장애가 난소적출에 의해 유발되었다. 한편 이러한 난소적출에 의한 에스트로겐 결핍성 폐경기 관련 갱년기 장애 소견이, 가감귀비온담탕 추출물 500, 250 및 125 mg/kg의 84일에 걸친 연속 경구 투여에 의해 투여 용량 의존적으로 억제되었다. 결 론: 이상의 결과에서, 가감귀비온담탕 500, 250 및 125 mg/kg의 경구투여는 난소적출 랫트에서 에스트로겐 결핍성 폐경기 관련 갱년기 장애 개선 효과를 투여 용량 의존적으로 나타내었다. 따라서 가감귀비온담탕은 효과적인 갱년기 장애 개선제로서 개발 가능성이 높을 것으로 기대되며, 특히 에스트로겐 결핍성 비만 및 골다공증의 개선에 유효할 것으로 판단된다. 한편 가감귀비온담탕은 총 18종의 약제로 구성되어 있고, 각각 수많은 생리활성 물질을 함유하고 있어, 이후 생리활성을 나타내는 화학성분의 검색과 더불어 다양한 방면으로 기전적인 연구가 체계적으로 수행해야 할 것으로 판단된다.

• 생명과학회지
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• 제18권11호
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• pp.1578-1583
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• 2008

폐경을 앞둔 여성에게는 폐경을 전후하여 지속되는 골 손실 가속화 등의 문제점을 가지고 있다. 그러므로 본 연구에서는 인위적 폐경을 유발시킨 난소 절제 쥐에서의 골 손실의 유무를 결합조직 중의 collagen 함량 변화를 통하여 그 효과를 검토하였다. 그 결과 생화학적 골 대사 지표인 혈 중 ALP 활성은 난소 절제(OVX-control)로 인하여 증가하는 반면, 난소 절제 후 다시마 추출물 투여(OVX-ST50, OVX-ST200)로 혈중 ALP 활성은 감소하는 경향을 보여 골 흡수를 저하시킬 수 있는 가능성을 나타내었다. 한편 난소 절제 후 collagen 함량이 감소하였으나, 다시마 추출물 투여에 의해 피부조직과 골.연골 조직에서 collagen 함량이 증가하는 경향을 보였고, 특히 OVX-ST200군은 각 조직 모두 OVX-control에 비하여 유의적으로 증가하였다(p<0.05). Collagen의 성숙 가교물질인 pyridinoline 함량 또한 난소 절제 후 골, 연골 조직 중에서 감소하였으나 다시마 추출물을 투여한 군에서 증가하는 경향을 나타내었다. 골에서의 deoxypylidinoline 함량은 난소를 절제하지 않은 Sham군이 OVX-control군에 비해서 유의적으로 높은 값을 나타냈고(p<0.05), 난소 절제 후 다시마 추출물을 농도별로 투여한 군(OVX-ST50 및 OVX-ST200)에서 유의 적으로 높은 값을 나타내어(p<0.05), 난소 절제 시 합성이 감소되는 deoxypyridinoline 생성량을증가시켰다. 에스트로겐 감소로 인한 결합조직 중 collagen 함량 저하가 다시마 추출물 투여에 의해 증가된 본 실험 결과로 미루어 보아 다시마 중의 phytoestrogen이 에스트로겐 유사효과를 나타냄을 알 수 있었다. 이상과 같이 폐경으로 인한 장애를 감소시키기 위하여 에스트로겐의 장기간 복용에 의한 부작용을 다시마 중의 phytoestrogen이 estrogen 대체 작용을 함으로써 그 부작용을 감소시켜 줄 것으로 사료되며, 이들의 구조 및 기전에 대해서는 앞으로 연구가 더 필요 한 것으로 생각된다.

• Toxicological Research
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• 제29권1호
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• pp.43-52
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• 2013

Zearalenone (ZEN) is a non-steroidal estrogenic mycotoxin produced by several species of Fusarium that are found in cereals and agricultural products. ZEN has been implicated in mycotoxicosis in farm animals and in humans. The toxic effects of ZEN are well known, but the ability of an alkaline Comet assay to assess ZEN-induced oxidative DNA damage in Chang liver cells has not been established. The first aim of this study was to evaluate the Comet assay for the determination of cytotoxicity and extent of DNA damage induced by ZEN toxin, and the second aim was to investigate the ability of N-acetylcysteine amide (NACA) to protect cells from ZEN-induced toxicity. In the Comet assay, DNA damage was assessed by quantifying the tail extent moment (TEM; arbitrary unit) and tail length (TL; arbitrary unit), which are used as indicators of DNA strand breaks in SCGE. The cytotoxic effects of ZEN in Chang liver cells were mediated by inhibition of cell proliferation and induction of oxidative DNA damage. Increasing the concentration of ZEN increased the extent of DNA damage. The extent of DNA migration, and percentage of cells with tails were significantly increased in a concentration-dependent manner following treatment with ZEN toxin (p < 0.05). Treatment with a low concentration of ZEN toxin (25 ${\mu}M$) induced a relatively low level of DNA damage, compared to treatment of cells with a high concentration of ZEN toxin (250 ${\mu}M$). Oxidative DNA damage appeared to be a key determinant of ZEN-induced toxicity in Chang liver cells. Significant reductions in cytolethality and oxidative DNA damage were observed when cells were pretreated with NACA prior to exposure to any concentration of ZEN. Our data suggest that ZEN induces DNA damage in Chang liver cells, and that the antioxidant activity of NACA may contribute to the reduction of ZEN-induced DNA damage and cytotoxicity via elimination of oxidative stress.

• 한국환경생물학회:학술대회논문집
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• 한국환경생물학회 2002년도 학술대회
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• pp.141-144
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• 2002

Environmental estrogens are natural or synthetic substances present in the aquatic environment, especially in effluent from sewage treatment. However, the adverse effects of these estrogenic substances on fish reproduction are unknown. Di-2-ethylhexyl phthalate (DEHP) is the most common phthalate, which Ps used as a plasticizer in polyvinylchloride (PVC), and it is widespread in the environment and has been found in aquatic organisms and sediments. Therefore, juvenile common carps (Cyprinus carpio) were exposed to nominal concentrations of 17$\beta$-estradiol (E2) (0.5, 5, 50 $\mu\textrm{g}$/L) and DEHP (10, 100, 500 $\mu\textrm{g}$/L) for 21 days, to determine the adverse reproductive effects of these compounds on plasma vitellogenin (VTG) induction, sex steroid level, and gonad weight. Electrophoresis (SDS-PAGE) revealed that much of VTG was induced in fish exposed to 5 and 50 E$_2$ $\mu\textrm{g}$/L, but none of DEHP exposure showed induction. Enzyme-linked immunosorbent assay (ELISA) revealed that VTG was significantly induced in fish exposed to 5 and 50 E$_2$ $\mu\textrm{g}$/L, and combination of 50 E$_2$ $\mu\textrm{g}$/L with 10 and 500 DEHP $\mu\textrm{g}$/L, but none of DEHP exposure showed induction. Analysis of sex steroid levels in some fish revealed that testosterone (T) was detected in both male and female fish of the control and DEHP exposures, but none of fish exposed to 22 concentrations had detectable testosterone level. On the other hand, E$_2$ exposure induced 17$\beta$-estradiol in plasma of male fish, but there was no induction of 17$\beta$-estradiol in plasma of male fish exposed to DEHP. Comparison of gonadosomatic index (GSI) revealed that maximal E$_2$ exposure inhibited ovarian growth, but maximal DEHP exposure stimulated testicular growth. The results indicated that those comparisons can be a useful bio-indicator for determining adverse reproductive effect of endocrine disrupting chemicals (EDCs).