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某自来水厂水源水有机提取物的雌激素样活性研究 被引量:1

Study on the Estrogenic Effects of Organic Extracts from Raw Water of a Waterworks
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摘要 [目的]了解某自来水厂水源水有机提取物的雌激素样活性。[方法]用固相萃取法富集水样,分低、中、高剂量染毒组(体外试验为每毫升染毒量分别相当于10、100、1000mL水源水中有机提取物的剂量;体内试验为每千克体重灌胃量相当于2、5、10、25L水源水中有机提取物的剂量)、阴性对照组和雌二醇阳性对照组,通过体外人乳腺癌(MCF-7)细胞增殖试验、报告基因试验和初断乳大鼠子宫增重试验对水源水有机提取物的雌激素样活性进行研究。[结果]体外细胞增殖试验中,高剂量组较阴性对照组出现细胞增殖效应(P<0.05),细胞增殖率为(130.85±13.68)%;而报告基因试验中,中剂量组检测到荧光强度增加(P<0.05),相对荧光强度为(207.67±12.40)%。子宫增重试验中,相当于低、中、高剂量染毒组大鼠子宫湿重和黏液重脏器系数与阴性对照组相比差异无统计学意义。[结论]体外试验表明水源水中含有雌激素样活性物质,但体内试验尚不能确定该水源水具有明确的雌激素样活性。 [ Objective ] To study the estrogenic effects of organic extracts from raw water of a waterworks. [ Methods ] The estrogenic effects of organic compounds which were extracted from raw water by solid phase extraction method were detected by MCF-7 cell proliferation assay, luciferase reporter gene assay and rodent uterotrophic bioassay. The exposure doses were equivalent to making organic extractions from 10, 100, 1000mL raw water condensed into 1 mL ethanol in vivo, and from 2, 5, 10, 25 mL cindensed into 1 mL ethanol in vivo. [ Results ] Compared with the negative control group, the significant cell proliferation effect was detected in the group of 1000mL water sample, corresponding proliferation rate was( 130.85 ± 13.68 )%. The luciferase activity in 100 mL water sample group increased significantly, relative fluorescence intensity was ( 207.67 ± 12.40 )%. Uterotrophic bioassay showed the relative weight of uterus and luminal contents of the organic extracts treated groups slightly increased compared with that of the vehicle control group, but the differences were not so significant. [ Conclusion ] In vitro assays showed that organic extracts from this raw water contained estrogen-like mixture, while in vivo assay didn't show definite estrogenic effects.
出处 《环境与职业医学》 CAS 北大核心 2010年第1期1-5,共5页 Journal of Environmental and Occupational Medicine
基金 国家自然科学基金(编号:20777042) 南通市社会发展项目(编号:S5039)
关键词 有机提取物 细胞增殖试验 报告基因试验 子宫增重试验 organic extracts cell proliferation assay reporter gene assay uterotrophic bioassay
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  • 1CARLSEN E, GIWERCMAN A, KEIDING N, et al, Evidence for decreasing quality of semen during past 50 years [J]. BMJ, 1992, 305( 6854 ): 609-613.
  • 2SWAN S H, ELKIN E P, FENSTER L. The question of declining sperm density revisited: an analysis of 101 studies published 1934-1996[ J ]. Environ Health Perspect, 2000, 108( 10 ): 961-966.
  • 3王俊虹,黄爱华,刘淑红.环境雌激素及其检测技术[J].中国公共卫生,2007,23(10):1231-1233. 被引量:3
  • 4王春,李晓东,杨自力,史玉坤,顾俊,王辉.南通市饮用水中邻苯二甲酸酯类含量调查[J].环境与健康杂志,2007,24(6):438-440. 被引量:21
  • 5张静云,吕剑,何义亮,靳强.环境雌激素的生物检测与应用[J].环境科学与技术,2007,30(2):100-102. 被引量:13
  • 6SOTO A M, MAFFINI M V, SCHAEBERLE C M, et al. Strengths and weaknesses of in vitro assays for estrogenic and androgenic activity[J]. Best Pract Res Clin Endocrinol Metab, 2006, 20( 1 ): 15-33.
  • 7SOTO AM, SONNENSCHEIN C, CHUNG K L, et al. The E-SCREEN assay as a tool to identify estrogens: an update on estrogenic environmental pollutants [ J J. Environ Health Perspect, 1995, 103 ( Suppl 7 ): 113-122.
  • 8CLODE S A. Assessment of in vivo assays for endocrine disruption[ J ]. Best Pract Res Clin Endocrinol Metab, 2006, 20( 1 ): 35-43.
  • 9OWENS JW, ASHBYJ. Critical review and evaluation of the uterotrophic bioassay for the identification of possible estrogen agonists and antagonists : in support of the validation of the OECD uterotrophic protocols for the laboratory rodent. Organisation for Economic Co-operation and Development[ J ]. Crit Rev Toxicol, 2002, 32( 6 ): 445-520.
  • 10张国州,张宇洁,王霞,殷丽红,蒋颂辉,朱惠刚,屈卫东.水源水有机物低剂量混合暴露的雌/雄激素效应[J].卫生研究,2006,35(2):171-174. 被引量:3

二级参考文献79

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  • 1潘尚霞(综述),张建鹏(综述),戴昌芳(审校).环境内分泌干扰物研究进展[J].中国环境卫生,2006,9(1):29-32. 被引量:11
  • 2Janowski T, Zdunczyk S, Malecki-Tepicht J, et al. Mammary secretion of oestrogens in the cow[J]. Domest Anita Endocrinol, 2002, 23 (1/2):125-137.
  • 3Peter W. Parodi. Impact of cows' milk estrogen on cancer risk[J]. International Dairy Journal, 2012, 22(1):3-14.
  • 4Newmark Harold L, Heaney Robert P. Dairy products and prostate cancer risk[J]. Nutrition and Cancer, 2010, 62(3):297-299.
  • 5Daniel W, Xia Xu, Timothy D, et al. Quantitative measurement of endogenous estrogen mctabolites, risk-factors for development of breast cancer, in commercial milk products by LC-MS/MS[J]. Journal of Chromatography B. 2009. 877(13):1327-1334.
  • 6Saravanabhavan G, Helleur R, Hellou J. GC - MS/MS measurement of natural and synthetic estrogens in receiving waters and mussels close to a raw sewage ocean outfall[J]. Chemosphere, 2009, 76(8), 1156-1162.
  • 7Wang S, Huang W, Fang GZ, et al. On-line Coupling of Solid-phase Extraction to High-performance Liquid Chromatography for Deter- mination of Estrogens in Environment [J]. Anal Chim Acta, 2008, 606(2):194-201.
  • 8Sun CF, Wu TL, Tsao KC, et al. Development of two ELISA for estrogen and progesterone receptor with sufficient sensitivity for fine needle aspirate and core biopsy[J]. Journal of Clinicak Laboratory Analysis, 2001, 15(3):138-143.
  • 9Liu S, Xie Z, Wu X, et al. Separation of structurally related estrogens using isocratic elution pressurized capillary electrochromatography [J]. Journal of Chromatography A, 2005, 1092(2):258-262.
  • 10Ji-Eun Ira, Jung-Ae Han, Byung Kun Kim, et al. Electrochemical detection of estrogen hormone by immobilized estrogen receptor on Au electrode[J]. Surface and Coatings Technology,2010,205(1):275- 278.

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