Andrews J E, Nichols H P, Schmid J E, Mole L M, Hunter E S, Klinefelter G R
National Health and Environmental Effects Research Laboratory, Reproductive Toxicology Division, United States Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Reprod Toxicol. 2004 Nov;19(1):111-6. doi: 10.1016/j.reprotox.2004.06.005.
The chlorination of drinking water results in production of numerous disinfection by-products (DBPs). One of the important classes of DBPs is the haloacetic acids. We have previously shown that the haloacetic acids (HAs), dichloro (DCA), dibromo (DBA) and bromochloro (BCA) acetic acid are developmentally toxic in mouse whole embryo culture. Human exposure to these contaminants in drinking water would involve simultaneous exposure to all three HAs. This study explores the question of developmental toxicity interactions between these compounds. Gestational day (GD) 9.5 rat embryos were exposed to various concentrations of the three HAs (singly or in combination) for 48 h and then evaluated for dysmorphology. The embryonic effects from exposure to the single compounds and mixtures were evaluated using developmental score (DEVSC) as the parameter of comparison. Concentrations of individual compounds and mixtures were chosen (based on a dose-additivity model) which were predicted to produce scores 10 or 20% lower than control levels. Evaluations were performed on all possible combinations of the three HAs. The HAs were dysmorphogenic and resulted in primarily rotation and heart defects and to a lesser extent prosencephalic, visceral arch, and eye defects. The percent anomalies in the rat were comparable to those previously published for the mouse at comparable toxicant concentration. There was a low incidence of neural tube defects in the rat following exposure to the HAs. The rat neural tube appeared less sensitive to the HAs than did the mouse resulting in a higher rate of neural tube dysmorphology in the mouse. Following exposures to BCA and DBA, alone and in combination, there was a significant incidence of delayed embryonic caudal development with apparent normal development anterior to the second visceral arch. The developmental scores for embryos exposed to combinations of the three compounds, when compared to scores for embryos exposed to the single compounds, indicated that the dose-additivity model adequately predicted the observed toxicity and that the developmental toxicity of these water disinfection by-products appears to be additive in whole embryo culture (WEC).
饮用水氯化会产生大量消毒副产物(DBP)。卤乙酸是重要的一类DBP。我们之前已表明,卤乙酸(HA)、二氯乙酸(DCA)、二溴乙酸(DBA)和溴氯乙酸(BCA)在小鼠全胚胎培养中具有发育毒性。人类通过饮用水接触这些污染物时会同时接触到所有三种HA。本研究探讨了这些化合物之间发育毒性相互作用的问题。在妊娠第9.5天,将大鼠胚胎暴露于不同浓度的三种HA(单独或组合)中48小时,然后评估其畸形情况。以发育评分(DEVSC)作为比较参数,评估暴露于单一化合物和混合物后的胚胎效应。根据剂量相加模型选择了个别化合物和混合物的浓度,预计这些浓度会使评分比对照水平低10%或20%。对三种HA的所有可能组合进行了评估。HA具有致畸性,主要导致旋转和心脏缺陷,在较小程度上导致前脑、内脏弓和眼睛缺陷。在可比的毒物浓度下,大鼠的异常百分比与之前发表的小鼠异常百分比相当。暴露于HA后,大鼠神经管缺陷的发生率较低。大鼠神经管对HA的敏感性似乎低于小鼠,导致小鼠神经管畸形的发生率更高。单独或联合暴露于BCA和DBA后,胚胎尾部发育延迟的发生率较高,第二内脏弓前方的发育明显正常。与暴露于单一化合物的胚胎评分相比,暴露于三种化合物组合的胚胎发育评分表明,剂量相加模型充分预测了观察到的毒性,并且这些水消毒副产物在全胚胎培养(WEC)中的发育毒性似乎是相加的。