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使用食蚊鱼和鳟鱼生物测定法测定全部废水的雄激素活性。

Determination of the androgenic potency of whole effluents using mosquitofish and trout bioassays.

作者信息

Bandelj E, van den Heuvel M R, Leusch F D L, Shannon N, Taylor S, McCarthy L H

机构信息

Ryerson University, Toronto, Ontario, Canada.

出版信息

Aquat Toxicol. 2006 Dec 1;80(3):237-48. doi: 10.1016/j.aquatox.2006.08.011. Epub 2006 Sep 25.

Abstract

This study combined bioassay-derived and direct chemical analysis of steroidal compounds in pulp and paper and municipal sewage effluent in order to determine the cause of masculinization of female mosquitofish. The bioassays used in this study consisted of androgen and estrogen receptor binding, and aromatase inhibition using tissues from rainbow trout. This study observed no masculinization of female mosquitofish from a pulp and paper mill effluent that was previously observed to cause this effect. Mosquitofish sampled from the receiving environment of the same mill verified that masculinization was not occurring in the wild. The municipal sewage effluent also had no masculinizing effect. In vitro bioassays indicated significant sources of both androgens and estrogens in the effluents tested with sewage effluent having both the highest estradiol (41 ng/L) and testosterone (182 ng/L) equivalent concentration. These results could not be attributed to any particular compounds measured in the effluents. Two compounds implicated in the masculinization of mosquitofish by pulp and paper effluent, androstenedione and androstadienedione required relatively large (10-100 microg/L) waterborne concentrations to elicit a masculinizing effect and neither of these compounds are likely to occur at levels this high in the natural environment. The potent aromatase inhibitor, 4-hydroxyandrostenedione also did not cause masculinization at 100 microg/L indicating that masculinization did not occur through this mechanism. The mammalian anti-androgen, cyproterone acetate was only partially effective in mosquitofish and reduced the severity of masculinization in the presence of methyl testosterone. While neither effluent masculinized mosquitofish, there was a significant reduction of in vitro ovarian steroid production with the most severe effects observed with the sewage effluent. Overall, this study found the disappearance of a masculinizing effect that had been previously observed; concluded that based on 21 days aqueous exposures androstenedione and androstadienedione are not likely candidates for mosquitofish masculinization, and showed that masculinization and in vitro steroid production are unrelated biological endpoints.

摘要

本研究结合了生物测定法以及对纸浆和造纸厂及城市污水中甾体化合物的直接化学分析,以确定雌性食蚊鱼雄性化的原因。本研究中使用的生物测定包括雄激素和雌激素受体结合,以及使用虹鳟鱼组织进行的芳香化酶抑制实验。本研究观察到,之前被观察到会导致这种效应的一家纸浆和造纸厂排放的污水,并未使雌性食蚊鱼雄性化。从同一家工厂的受纳环境中采集的食蚊鱼证实,野外并未发生雄性化现象。城市污水也没有雄性化作用。体外生物测定表明,在所测试的污水中,雄激素和雌激素的来源都很显著,污水中的雌二醇(41纳克/升)和睾酮(182纳克/升)等效浓度最高。这些结果不能归因于污水中检测到的任何特定化合物。纸浆和造纸厂污水中与食蚊鱼雄性化有关的两种化合物,雄烯二酮和雄二烯二酮,需要相对较高(10 - 100微克/升)的水体浓度才能引发雄性化效应,而在自然环境中,这两种化合物都不太可能达到如此高的水平。强效芳香化酶抑制剂4 - 羟基雄烯二酮在100微克/升时也未导致雄性化,这表明雄性化并非通过这种机制发生。哺乳动物抗雄激素醋酸环丙孕酮在食蚊鱼中仅部分有效,并且在甲基睾酮存在的情况下会降低雄性化的严重程度。虽然两种污水都未使食蚊鱼雄性化,但体外卵巢甾体生成显著减少,其中以城市污水的影响最为严重。总体而言,本研究发现之前观察到的雄性化效应消失了;得出结论,基于21天的水体暴露,雄烯二酮和雄二烯二酮不太可能是食蚊鱼雄性化的原因,并表明雄性化和体外甾体生成是不相关的生物学终点。

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