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利用基于体外生物活性测定的安全对照化合物值对人类暴露于雌激素的下一代风险进行评估。

Next generation risk assessment of human exposure to estrogens using safe comparator compound values based on in vitro bioactivity assays.

机构信息

Division of Toxicology, Wageningen University and Research, 6700 EA, Wageningen, The Netherlands.

Unilever Safety and Environmental Assurance Centre, Sharnbrook, Bedfordshire, MK44 1LQ, UK.

出版信息

Arch Toxicol. 2023 Jun;97(6):1547-1575. doi: 10.1007/s00204-023-03480-w. Epub 2023 Apr 22.

Abstract

In next generation risk assessment (NGRA), the Dietary Comparator Ratio (DCR) can be used to assess the safety of chemical exposures to humans in a 3R compliant approach. The DCR compares the Exposure Activity Ratio (EAR) for exposure to a compound of interest (EAR) to the EAR for an established safe exposure level to a comparator compound (EAR), acting by the same mode of action. It can be concluded that the exposure to a test compound is safe at a corresponding DCR ≤ 1. In this study, genistein (GEN) was selected as a comparator compound by comparison of reported safe internal exposures to GEN to its BMCL, as no effect level, the latter determined in the in vitro estrogenic MCF7/Bos proliferation, T47D ER-CALUX, and U2OS ERα-CALUX assay. The EAR was defined using the BMCL and EC values from the 3 in vitro assays and subsequently used to calculate the DCRs for exposures to 14 test compounds, predicting the (absence of) estrogenicity. The predictions were evaluated by comparison to reported in vivo estrogenicity in humans for these exposures. The results obtained support in the DCR approach as an important animal-free new approach methodology (NAM) in NGRA and show how in vitro assays can be used to define DCR values.

摘要

在下一代风险评估 (NGRA) 中,可以使用膳食比较比 (DCR) 来评估符合 3R 原则的人类化学暴露的安全性。DCR 将感兴趣化合物的暴露活动比 (EAR) 与比较化合物 (EAR) 的已建立安全暴露水平的 EAR 进行比较,EAR 通过相同的作用方式起作用。可以得出结论,当相应的 DCR ≤ 1 时,测试化合物的暴露是安全的。在这项研究中,通过将 GEN 的报告安全内部暴露与 BMCL(无作用水平)进行比较,选择 GEN 作为比较化合物,后者是在体外雌激素 MCF7/Bos 增殖、T47D ER-CALUX 和 U2OS ERα-CALUX 测定中确定的。EAR 是使用来自 3 种体外测定的 BMCL 和 EC 值定义的,随后用于计算 14 种测试化合物暴露的 DCR,预测(不存在)雌激素性。通过将这些暴露的报告体内雌激素活性进行比较,评估了预测结果。所得结果支持 DCR 方法作为下一代风险评估中的一种重要的无动物新方法 (NAM),并展示了如何使用体外测定来定义 DCR 值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae42/10182946/11f643e2a7ee/204_2023_3480_Fig1_HTML.jpg

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