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17β-雌二醇的水相氯化产物及其雌激素活性。

Products of aqueous chlorination of 17beta-estradiol and their estrogenic activities.

作者信息

Hu Jianying, Cheng Shuijie, Aizawa Takako, Terao Yoshiyasu, Kunikane Shoichi

机构信息

College of Environmental Science, Peking University, Beijing, 100871 China.

出版信息

Environ Sci Technol. 2003 Dec 15;37(24):5665-70. doi: 10.1021/es034324+.

Abstract

To assess the estrogenic activity potentially stemming from 17beta-estradiol (E2) in drinking water, ESI-LC-MS was used to identifythe products of its aqueous chlorination under the following conditions: 50 microg/L E2, 1.46 mg/L sodium hypochlorite, pH 7.5, 25 degrees C. Seven products, including 2,4-dichloro-17beta-estradiol, monochloroestrone, 2,4-dichloroestrone, and the four byproducts such as 4-[2-(2,6-dichloro-3-hydroxyphenyl)ethyl]-7alpha-methyloctahydroinden-5-one (product C in the text) were identified in chlorinated E2 solution. The estrogenic activities of the aqueous chlorinated E2 solution at 10, 30, 60, 120, and 180 min contact time were assessed by a yeast two-hybrid system based on the ligand-dependent interaction of two proteins, a human estrogen receptor (ER) and a coactivator. All five solutions elicited transcriptional activation induction. The maximal beta-galactosidase activities induced by the chlorinated solution at 10, 30, and 60 min were similar and slightly lower than those before chlorination, while the activities of the chlorinated solution at 120 and 180 min were about 40% of those before chlorination. Finally, 4-chloro-17beta-estradiol (4-chloro-E2) (we failed to synthesize the 2-chloroestrone (2-chloro-E1)), 2,4-dichloro-17beta-estradiol (2,4-dichloro-E2), and 2,4-dichloroestrone (2,4-dichloro-E1) were synthesized, and product C was fractionated by HPLC. It was found that 4-chloro-E2 elicited strong estrogenic activity, at almost the same level as that of estrone (EC50 = 10(2) nM), while 2,4-dichloro-E2 elicited weaker beta-galactosidase activity compared with that of 4-chloro-E2. The EC50 was ca. 10(3) nM. The maximal beta-galactosidase activity for 2,4-dichloro-E1 was lower than that of 2,4-dichloro-E2, while its EC50 was similar to that of 2,4-dichloro-E2. In addition, product C, 4-[2-(2,6-dichloro-3-hydroxyphenyl)ethyl]-7alpha-methyloctahydroinden-5-one, induced high beta-galactosidase activity at the relatively higher concentration of 3.5 x 10(5) nM. On the basis of the dose-response curve of a single byproduct of chlorinated E2, the estrogenic activity at 120 and 180 min appears to be induced mainly by 2,4-dichloro-E2 and 2,4-dichloro-E1.

摘要

为评估饮用水中可能源于17β-雌二醇(E2)的雌激素活性,采用电喷雾电离液相色谱-质谱联用(ESI-LC-MS)在以下条件下鉴定其水相氯化产物:50微克/升E2、1.46毫克/升次氯酸钠、pH 7.5、25℃。在氯化E2溶液中鉴定出7种产物,包括2,4-二氯-17β-雌二醇、一氯雌酮、2,4-二氯雌酮以及4-[2-(2,6-二氯-3-羟基苯基)乙基]-7α-甲基八氢茚-5-酮(文中产物C)等4种副产物。基于人雌激素受体(ER)和共激活因子这两种蛋白质的配体依赖性相互作用,通过酵母双杂交系统评估了在接触时间为10、30、60、120和180分钟时水相氯化E2溶液的雌激素活性。所有5种溶液均引发转录激活诱导。氯化溶液在10、30和60分钟时诱导的最大β-半乳糖苷酶活性相似,略低于氯化前,而在120和180分钟时氯化溶液的活性约为氯化前的40%。最后,合成了4-氯-17β-雌二醇(4-氯-E2)(我们未能合成2-氯雌酮(2-氯-E1))、2,4-二氯-17β-雌二醇(2,4-二氯-E2)和2,4-二氯雌酮(2,4-二氯-E1),并通过高效液相色谱法对产物C进行了分离。结果发现,4-氯-E2引发强烈的雌激素活性,几乎与雌酮处于同一水平(半数有效浓度(EC50)=10²纳摩尔),而与4-氯-E2相比,2,4-二氯-E2引发的β-半乳糖苷酶活性较弱。其EC50约为10³纳摩尔。2,4-二氯-E1的最大β-半乳糖苷酶活性低于2,4-二氯-E2,但其EC50与2,4-二氯-E2相似。此外,产物C,即4-[2-(2,6-二氯-3-羟基苯基)乙基]-7α-甲基八氢茚-5-酮,在相对较高浓度3.5×10⁵纳摩尔时诱导出较高的β-半乳糖苷酶活性。基于氯化E2单一副产物的剂量反应曲线,120和180分钟时的雌激素活性似乎主要由2,4-二氯-E2和2,4-二氯-E1诱导产生。

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