Mid-Continent Ecology Division, United States Environmental Protection Agency, Duluth, Minnesota 55804, USA.
Toxicol Sci. 2013 Jun;133(2):225-33. doi: 10.1093/toxsci/kft068. Epub 2013 Mar 14.
Adaptive or compensatory responses to chemical exposure can significantly influence in vivo concentration-duration-response relationships. This study provided data to support development of a computational dynamic model of the hypothalamic-pituitary-gonadal axis of a model vertebrate and its response to aromatase inhibitors as a class of endocrine active chemicals. Fathead minnows (Pimephales promelas) were either exposed to the aromatase inhibitor fadrozole (0.5 or 30 μg/l) continuously for 1, 8, 12, 16, 20, 24, or 28 days or exposed for 8 days and then held in control water (no fadrozole) for an additional 4, 8, 12, 16, or 20 days. The time course of effects on ovarian steroid production, circulating 17β-estradiol (E2) and vitellogenin (VTG) concentrations, and expression of steroidogenesis-related genes in the ovary was measured. Exposure to 30 μg fadrozole/l significantly reduced plasma E2 and VTG concentrations after just 1 day and those effects persisted throughout 28 days of exposure. In contrast, ex vivo E2 production was similar to that of controls on day 8-28 of exposure, whereas transcripts coding for aromatase and follicle-stimulating hormone receptor were elevated, suggesting a compensatory response. Following cessation of fadrozole exposure, ex vivo E2 and plasma E2 concentrations exceeded and then recovered to control levels, but plasma VTG concentrations did not, even after 20 days of depuration. Collectively these data provide several new insights into the nature and time course of adaptive responses to an aromatase inhibitor that support development of a computational model (see companion article).
化学物质暴露的适应性或代偿性反应会显著影响体内浓度-时间-反应关系。本研究提供的数据支持建立一个模型脊椎动物下丘脑-垂体-性腺轴的计算动态模型,以及该模型对芳香酶抑制剂作为一类内分泌活性化学物质的反应。翻车鱼(Pimephales promelas)连续暴露于芳香酶抑制剂法舒地尔(0.5 或 30μg/l)1、8、12、16、20、24 或 28 天,或暴露于 8 天,然后在不含法舒地尔的对照水中再保留 4、8、12、16 或 20 天。测量了对卵巢类固醇生成、循环 17β-雌二醇(E2)和卵黄蛋白原(VTG)浓度以及卵巢中类固醇生成相关基因表达的影响的时间进程。暴露于 30μg/l 法舒地尔仅 1 天后,血浆 E2 和 VTG 浓度显著降低,这些影响持续到暴露 28 天。相比之下,在暴露 8-28 天期间,离体 E2 产生与对照相似,而编码芳香酶和促卵泡激素受体的转录物升高,表明存在代偿性反应。停止法舒地尔暴露后,离体 E2 和血浆 E2 浓度超过并恢复到对照水平,但血浆 VTG 浓度未恢复,即使在 20 天的净化后也是如此。这些数据共同为芳香酶抑制剂的适应性反应的性质和时间进程提供了一些新的见解,支持了计算模型的开发(见相关文章)。