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1
Quantitative Response-Response Relationships Linking Aromatase Inhibition to Decreased Fecundity are Conserved Across Three Fishes with Asynchronous Oocyte Development.定量反应-反应关系将芳香酶抑制与生育力下降联系起来,这种关系在三种具有不同步卵母细胞发育的鱼类中是保守的。
Environ Sci Technol. 2019 Sep 3;53(17):10470-10478. doi: 10.1021/acs.est.9b02606. Epub 2019 Aug 14.
2
Differential Sensitivity to In Vitro Inhibition of Cytochrome P450 Aromatase (CYP19) Activity Among 18 Freshwater Fishes.18 种淡水鱼类细胞色素 P450 芳香酶(CYP19)活性的体外抑制的差异敏感性。
Toxicol Sci. 2019 Aug 1;170(2):394-403. doi: 10.1093/toxsci/kfz115.
3
Rapid effects of the aromatase inhibitor fadrozole on steroid production and gene expression in the ovary of female fathead minnows (Pimephales promelas).芳香化酶抑制剂法倔唑对雌性黑头软口鲦(Pimephales promelas)卵巢类固醇生成和基因表达的快速影响。
Gen Comp Endocrinol. 2017 Oct 1;252:79-87. doi: 10.1016/j.ygcen.2017.07.022. Epub 2017 Jul 21.
4
Quantitative Adverse Outcome Pathways and Their Application to Predictive Toxicology.定量不良结局途径及其在预测毒理学中的应用。
Environ Sci Technol. 2017 Apr 18;51(8):4661-4672. doi: 10.1021/acs.est.6b06230. Epub 2017 Apr 7.
5
How Adverse Outcome Pathways Can Aid the Development and Use of Computational Prediction Models for Regulatory Toxicology.不良结局途径如何助力监管毒理学计算预测模型的开发与应用。
Toxicol Sci. 2017 Feb;155(2):326-336. doi: 10.1093/toxsci/kfw207. Epub 2016 Dec 19.
6
Editor's Highlight: Computational Modeling of Plasma Vitellogenin Alterations in Response to Aromatase Inhibition in Fathead Minnows.编辑推荐:黑头软口鲦鱼中血浆卵黄蛋白原变化对芳香酶抑制反应的计算模型
Toxicol Sci. 2016 Nov;154(1):78-89. doi: 10.1093/toxsci/kfw142. Epub 2016 Aug 7.
7
Editor's Highlight: Analysis of the Effects of Cell Stress and Cytotoxicity on In Vitro Assay Activity Across a Diverse Chemical and Assay Space.编辑推荐:在不同化学物质和检测体系中分析细胞应激和细胞毒性对体外检测活性的影响
Toxicol Sci. 2016 Aug;152(2):323-39. doi: 10.1093/toxsci/kfw092. Epub 2016 May 20.
8
High-Throughput Screening of Chemical Effects on Steroidogenesis Using H295R Human Adrenocortical Carcinoma Cells.使用H295R人肾上腺皮质癌细胞对类固醇生成的化学效应进行高通量筛选
Toxicol Sci. 2016 Apr;150(2):323-32. doi: 10.1093/toxsci/kfw002. Epub 2016 Jan 18.
9
Increasing Scientific Confidence in Adverse Outcome Pathways: Application of Tailored Bradford-Hill Considerations for Evaluating Weight of Evidence.增强对不良结局途径的科学信心:运用定制的布拉德福德-希尔考量因素评估证据权重
Regul Toxicol Pharmacol. 2015 Aug;72(3):514-37. doi: 10.1016/j.yrtph.2015.04.004. Epub 2015 Apr 8.
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Regioselective hydroxylation of steroid hormones by human cytochromes P450.甾体激素的人细胞色素 P450 的区域选择性羟化作用。
Drug Metab Rev. 2015 May;47(2):89-110. doi: 10.3109/03602532.2015.1011658. Epub 2015 Feb 13.

21 世纪生态毒理学案例研究:利用体外芳香酶抑制数据预测成年雌性鱼类的短期体内反应。

Case Study in 21st Century Ecotoxicology: Using In Vitro Aromatase Inhibition Data to Predict Short-Term In Vivo Responses in Adult Female Fish.

机构信息

US Environmental Protection Agency, Great Lakes Toxicology and Ecology Division, Duluth, Minnesota.

US Environmental Protection Agency, Integrated Systems Toxicology Division, Research Triangle Park, North Carolina.

出版信息

Environ Toxicol Chem. 2021 Apr;40(4):1155-1170. doi: 10.1002/etc.4968. Epub 2021 Mar 10.

DOI:10.1002/etc.4968
PMID:33332681
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8127875/
Abstract

The present study evaluated whether in vitro measures of aromatase inhibition as inputs into a quantitative adverse outcome pathway (qAOP) construct could effectively predict in vivo effects on 17β-estradiol (E2) and vitellogenin (VTG) concentrations in female fathead minnows. Five chemicals identified as aromatase inhibitors in mammalian-based ToxCast assays were screened for their ability to inhibit fathead minnow aromatase in vitro. Female fathead minnows were then exposed to 3 of those chemicals: letrozole, epoxiconazole, and imazalil in concentration-response (5 concentrations plus control) for 24 h. Consistent with AOP-based expectations, all 3 chemicals caused significant reductions in plasma E2 and hepatic VTG transcription. Characteristic compensatory upregulation of aromatase and follicle-stimulating hormone receptor (fshr) transcripts in the ovary were observed for letrozole but not for the other 2 compounds. Considering the overall patterns of concentration-response and temporal concordance among endpoints, data from the in vivo experiments strengthen confidence in the qualitative relationships outlined by the AOP. Quantitatively, the qAOP model provided predictions that fell within the standard error of measured data for letrozole but not for imazalil and epoxiconazole. However, the inclusion of measured plasma concentrations of the test chemicals as inputs improved model predictions, with all predictions falling within the range of measured values. Results highlight both the utility and limitations of the qAOP and its potential use in 21st century ecotoxicology. Environ Toxicol Chem 2021;40:1155-1170. © 2020 SETAC. This article has been contributed to by US Government employees and their work is in the public domain in the USA.

摘要

本研究评估了体外芳香酶抑制测定作为定量不良结局途径(qAOP)构建的输入,是否能有效预测对雌性黑头呆鱼 17β-雌二醇(E2)和卵黄蛋白原(VTG)浓度的体内影响。在哺乳动物基于 ToxCast 测定的芳香酶抑制剂中筛选了 5 种化学物质,以评估其抑制黑头呆鱼芳香酶的能力。然后,将 3 种化学物质(来曲唑、环氧氯丙烷和双氰胺)暴露于雌性黑头呆鱼 24 h 的浓度反应(5 个浓度加对照)中。与基于 AOP 的预期一致,所有 3 种化学物质均导致血浆 E2 和肝 VTG 转录显著降低。来曲唑引起卵巢芳香酶和促滤泡激素受体(fshr)转录物的特征性补偿性上调,但其他 2 种化合物则没有。考虑到体内实验终点的浓度反应和时间一致性的整体模式,实验数据增强了 AOP 概述的定性关系的信心。从定量上看,qAOP 模型对来曲唑的预测与实测数据的标准误差相符,但对双氰胺和环氧氯丙烷的预测则不然。然而,将测试化学物质的实测血浆浓度作为输入纳入模型,提高了模型预测的准确性,所有预测值均在实测值范围内。结果突出了 qAOP 的实用性和局限性,及其在 21 世纪生态毒理学中的潜在应用。Environ Toxicol Chem 2021;40:1155-1170。 © 2020 SETAC。本文的作者为美国政府雇员,其作品在美国属于公有领域。