• Asian Pacific Journal of Cancer Prevention
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• 제15권13호
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• pp.5117-5121
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• 2014

Endocrine-disrupting chemicals (EDCs) have been reported to interfere with estrogen signaling. Exposure to these chemicals decreases the immune response and causes a wide range of diseases in animals and humans. Recently, many studies showed that licorice (Glycyrrhiza glabra) root extract (LRE) commonly called "gamcho" in Korea exhibits antioxidative, chemoprotective, and detoxifying properties. This study aimed to investigate the mechanism of action of LRE and to determine if and how LRE can alleviate the toxicity of EDCs. LRE was prepared by vacuum evaporation and freeze-drying after homogenization of licorice root powder that was soaked in 80% ethanol for 72 h. We used 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) as an EDC, which is known to induce tumors or cancers; MCF-7 breast cancer cells were used as a tumorigenic model. These were treated with TCDD and various concentrations of LRE (0, 50, 100, 200, $400{\mu}g/mL$) for 24, 48, and 72 h. As a result, TCDD stimulated MCF-7 cell proliferation, but LRE significantly inhibited TCDD-induced MCF-7 cell proliferation in a dose- and time-dependent manner. Expression of TCDD toxicity-related genes, i.e., aryl hydrocarbon receptor (AhR), AhR nuclear translocator, and cytochrome P450 1A1, were subsequently down-regulated by LRE in a dose-dependent manner. Analysis of cell cycle distribution after treatment of MCF-7 cells with TCDD and various concentrations of LRE showed that LRE inhibited the proliferation of MCF-7 cells via G2/M phase arrest. Reverse transcription-polymerase chain reaction and Western blot analyses also revealed that LRE dose-dependently increased the expression of the tumor suppressor genes p53 and p27 and down-regulated the expression of cell cycle-related genes. These data suggest that LRE can mitigate the tumorigenic effects of TCDD in breast cancer cells by suppression of AhR expression and cell cycle arrest. Thus, LRE can be used as a potential toxicity-alleviating agent against EDC-mediated disease.

• 한국발생생물학회지:발생과생식
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• 제11권3호
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• pp.179-185
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• 2007

Estrogen과 estrogenic endocrine disrupting chemicals(EDCs)는 주로 스테로이드 수용체와 작용하여 다양한 표적 단백질 유전자의 전사를 조절한다. 구조적으로 estrogen 수용체와 유사한 estrogen 수용체형 수용체(estrogen receptorrelated receptor, ERR)는 포유동물에서 배발생 후기에 외배엽 형성과 관련되어 있다고 알려진 고아핵수용체(orphan nuclear receptor)이다. 본 연구에서는 해양무척추동물인 둥근성게(Strongylocentrotus nudus)의 발생배를 재료로 estradiol-$17{\beta}(E_2)$과 EDCs의 일종인 nonylphenol(NP)이 발생과정의 형태학적 변화와 $ERR{\beta}$ like 1의 mRNA발현에 미치는 영향을 조사하였다. $E_2$와 NP가 처리된 발생배는 발생속도가 지연되었으며, 초기 유생기에 가까운 후기배의 비정상적인 발달형태가 관찰되었다. 수정란부터 초기 유생기까지 측정한 결과, 이들 화학물질에 의해 $ERR{\beta}$ like 1 mRNA는 포배기에 급격히 감소하는 패턴을 보였다. 이상의 결과는 둥근성게의 초기 배가 $E_2$와 NP에 의해 비정상적으로 발생되며, $ERR{\beta}$ like 1의 감소가 이 비정상적 배발생과 관련되어 있음을 시사한다.

• 농약과학회지
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• 제7권3호
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• pp.188-197
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• 2003

내분비교란물질은 동물에서 생식기계통을 통제하는 호르몬 조절에 영향을 준다. 상기 선정된 농약을 투여함에 있어서 실험동물로 Xiphophorus helleri로 선정하였는데 이는 암수의 구별이 육안적으로 명확히 관찰되며 또한 난태생으로 사육이 용이한 점이 있다. Xiphophorus helleri에 있어서 내분비교란물질로 의심되는 endosulfan과 molinate의 영향을 조사하기 위하여 vitellogenin과 aromatase 를 진단 biomarker로써 사용하였다. RT-PCR 결과 endosulfan과 molinate의 혼합처치군 및 alachlor 단독군 수컷에서 vitellogenin과 aromatase의 induction 이 동시에 관찰되었고, endosulfan 단독군에서는 aromatase의 induction이 관찰되었다. 본 실험에서는 endosulfan이나 molinate 단독 처치군에서의 성호르몬과 세포에 대한 유해 효과는 나타나지 않았다. 그러나, endosulfan과 molinate 의 혼합처치군에서는 vitellogenin과 aromatase의 발현 및 apoptosis가 관찰되었다. 이러한 결과는 swordtail fish에 영향을 미치지 않는 낮은 농도의 molinate와 endosulfan이라도 병용되는 경우에 생식기계의 호르몬 변화와 apoptosis를 야기시킨다는 사실을 제시한다.

• 농약과학회지
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• 제8권2호
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• pp.95-102
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• 2004

현재 국내 사용중이며 내분비계 장애추정농약으로 분류된 benomyl, carbaryl, endosulfan등 17종 농약에 대한 estrogen성 영향을 검색하기 위하여 인체난소암세포(BG1Luc4E2)를 이용한 luciferase assay를 수행하였으며, luciferase assay에서 Eeq를 산출한 후 내분비계 장애추정 농약의 에스트로겐성 영향에 대한 식이섭취 위험도 평가를 실시하였다. Estrogen 수용체 결합시험에서 cypermethrin, dicofol, endosulfan, esfenvalerate 및 fenvalerate가 $10^{-5}$ M에서 최고 영향이 관찰되었고, mancozeb 등 8종 농약은 약한 영향이 관찰되었으며, benomyl 등 나머지 4종 농약은 영향이 없었다. 이들 중 활성이 비교적 강한 dicofol 및 endoeulfan의 1 nmol 17 $\beta$-estradiol에 대한 RLP 와 RLU는 dicofol의 경우 $10^{-5}$ 및 56%이었구, endosulfan은 $10^{-5}$ 및 72%이었다. MRL을 이용한 식이섭취 위험도 평가 결과 농약들의 추청 1일 최대농약섭취량은 cypermethrin 0.667, dicofol 0.1462, endosulfan 0.2066 및 lenvalerate/esfenvalerate 0.2098 mg/person으로 총 추정 1일 최대 농약섭취량이 1.2298 mg/person이었고, 남성 혈중 에스트로겐 증가 농도는 3.075 ng/L로 정상농도에 비해 15%정도 증가하였으나, 국내 모니터링 성적을 기준으로 평가한 결과 남성혈중 에스트로겐 증가 농도는 0.01938 ng/L로 정상농도에 비해 0.09693%정도 증가하였다.

• Animal cells and systems
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• 제13권3호
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• pp.339-344
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• 2009

This study aims to find out the effect of heavy metals, as is the case of EDCs (endocrine disrupting chemicals), on reproductive endocrine disruption of aquatic animals. In the present experiment zinc, which is a heavy metal well known for its androgenous activity, was used. The experimental period was 24 weeks, starting in November during the inactive stage of the clam's reproductive cycle. The experimental groups were composed of one control condition and three zinc exposure conditions (0.64, 1.07, and 1.79 mg/L). The sex ratio (F:M) was 1:1.06 in the control group and 1:1.70 in all the exposed group, illustrating the tendency for higher proportion of males with increases in zinc concentration. Gonad maturity was higher in 1.07, and 1.79 mg/L groups compared to the control group, with higher maturity observed in males than females. Intersex individuals made up 24.7% of the exposed group, while females exhibited a higher ratio than the males with increasing zinc concentration. The results of this study indicate that zinc functions as an androgenic effector on the reproduction of Gomphina veneriformis.

• 공업화학
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• 제17권2호
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• pp.119-124
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• 2006

물 속에 존재하는 자연 유기물의 성분은 계절과 장소에 따라 다양하게 변하므로 이들 성분에 대한 고찰과 이들이 환경에 미치는 영향을 고찰할 필요가 있다. 본 총설에서는 물 속에 존재하는 휴믹 물질, 탄수화물, 단백질(아미노산), hexosamine, 유지, 오일, 그리스 및 미량 유기물질(내분비교란화학물질과 의약품) 등의 자연 유기물의 특성을 정리하였다.

• 한국환경보건학회:학술대회논문집
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• 한국환경보건학회 2005년도 Proceedings of KSEH.Minamata Forum
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• pp.54-57
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• 2005

Endocrine disrupting effects of several pharmaceutical products were evaluated with fish. The test pharmaceuticals(caffeine, ketoconazole, acetaminophen and diltiazem) have been often detected in aquatic environment of Korea(from on going study of this research team). We analyzed vitellogenin induction by qualitative (Western blot) and quantitative (ELISA) assay. $17{\beta}$ -estradiol was used as a positive control. Some pharmaceuticals could give effects to male Oryzias latipes. They could induced vitellogenin under exposure of chemicals at male Oryzias latipes.

• 한국환경보건학회:학술대회논문집
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• 한국환경보건학회 2005년도 가을학술대회
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• pp.179-182
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• 2005

Endocrine disrupting effects of several pharmaceutical products were evaluated with fish. The test pharmaceuticals(caffeine, ketoconazole, acetaminophen and diltiazem) have been often detected in aquatic environment of Korea(from on going study of this research team). We analyzed vitellogenin induction by qualitative (Western blot) and quantitative (ELISA) assay. $17{\beta}-estradiol$ was used as a positive control. Some pharmaceuticals could give effects to male Oryzias latipes. They could induced vitellogenin under exposure of chemicals at male Oryzias latipes.

• Bulletin of the Korean Chemical Society
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• 제23권3호
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• pp.432-436
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• 2002

Benomyl, one of the known endocrine disrupting chemicals, was analyzed to understand the fate in the nature. Water, sediment and biota samples are acidified to hydrolyze benomyl into carbendazim then followed by extraction and concentration. The concentrations of carbendazim in the samples were determined by liquid chromatography/time-of-flight mass spectrometer. Analysis data showed that certain amount of carbendazim was accumulated in sediment. On the contrary, no sign of accumulation in biota was observed probably due to the increased degradation rate in vivo. It is, however, that no one can claim carbendazim is not harmful to biota, since carbendazim may give a negative effect against organisms at the point of intaking.

• 한국독성학회:학술대회논문집
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• 한국독성학회 2006년도 추계학술대회
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• pp.34-45
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• 2006

Chemical toxicants are metabolically converted to numerous metabolites in the body. Toxicokinetic characteristics of metabolites could be therefore used as biomarker of exposure for human risk assessment. Biologically based dose response (BBDR) model was proposed for future direction of risk assessment. However, this area has not been developed well enough for human application. Benzo(a)pyrene (BP), for example, is a well-known environmental carcinogen and may produce more than 100 metabolites and BPDE-DNA adduct, a covalently bound form of DNA with benzo(a)pyrene diolepoxides (BPDES), has been applied to qualitatively or quantitaively estimate human exposure to BP. In addition, di(2-ethylhexyl) phthalate (DEHP), a widely used plasticize. in the polymer industry, is one of endocrine-disrupting chemicals (EDCs) and has been monitored in humans using urinary or serum concentrations of DEHP or its monomer MEHP for exposure and risk assessment. However, it is difficult to estimate the actual level of toxicants using these biomarkers in humans using. This presentation will discuss a methodology of exposure and risk assessment by application of metabolic profiling kinetics.