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跨物种比较人源和非洲爪蟾碘酪氨酸脱碘酶的化学抑制作用。

Cross-species comparison of chemical inhibition of human and Xenopus iodotyrosine deiodinase.

机构信息

Great Lakes Toxicology and Ecology Division, Office of Research and Development, Center for Computational Toxicology and Exposure, U.S. Environmental Protection Agency, 6201 Congdon Blvd, Duluth, MN 55804, USA.

Great Lakes Toxicology and Ecology Division, Office of Research and Development, Center for Computational Toxicology and Exposure, U.S. Environmental Protection Agency, 6201 Congdon Blvd, Duluth, MN 55804, USA.

出版信息

Aquat Toxicol. 2022 Aug;249:106227. doi: 10.1016/j.aquatox.2022.106227. Epub 2022 Jun 15.

Abstract

The transition to include in vitro-based data in chemical hazard assessment has resulted in the development and implementation of screening assays to cover a diversity of biological pathways, including recently added assays to interrogate chemical disruption of proteins relevant to thyroid signaling pathways. Iodotyrosine deiodinase (IYD), the iodide recycling enzyme, is one such thyroid-relevant endpoint for which a human-based screening assay has recently been developed and used to screen large libraries of chemicals. Presented here is the development of an amphibian IYD inhibition assay and its implementation to conduct a cross-species comparison between chemical inhibition of mammalian and non-mammalian IYD enzyme activity. The successful development of an amphibian IYD inhibition assay was based on demonstration of sufficient IYD enzyme activity in several tissues collected from larval Xenopus laevis. With this new assay, 154 chemicals were tested in concentration-response to provide a basis for comparison of relative chemical potency to results obtained from the human IYD assay. Most chemicals exhibited similar inhibition in both assays, with less than 25% variation in median inhibition for 120 of 154 chemicals and 85% concordance in categorization of "active" (potential IYD inhibitor) versus "inactive". For chemicals that produced 50% or greater inhibition in both assays, rank-order potency was similar, with the majority of the IC50s varying by less than 2-fold (and all within an order of magnitude). Most differences resulted from greater maximum inhibition or higher chemical potency observed with human IYD. This strong cross-species agreement suggests that results from the human-based assay would be conservatively predictive of chemical effects on amphibian IYD.

摘要

将基于体外的数据纳入化学危害评估的转变导致了筛选测定法的开发和实施,以涵盖多种生物途径,包括最近增加的测定法以探究与甲状腺信号通路相关的蛋白质的化学干扰。碘酪氨酸脱碘酶(IYD)是一种与甲状腺相关的终点,最近已经开发出了基于人类的筛选测定法来筛选大量的化学物质。本文介绍了一种两栖动物 IYD 抑制测定法的开发及其在哺乳动物和非哺乳动物 IYD 酶活性的化学抑制的种间比较中的应用。成功开发两栖动物 IYD 抑制测定法的基础是证明从幼年非洲爪蟾(Xenopus laevis)收集的几种组织中存在足够的 IYD 酶活性。利用这种新的测定法,对 154 种化学物质进行了浓度反应测试,为比较人类 IYD 测定法获得的相对化学效力提供了基础。大多数化学物质在两种测定法中均表现出相似的抑制作用,在 154 种化学物质中,有 120 种化学物质的中位数抑制率的变化小于 25%,并且在“活性”(潜在的 IYD 抑制剂)与“非活性”的分类中,有 85%的一致性。对于在两种测定法中均产生 50%或更高抑制作用的化学物质,其效力排序相似,大多数 IC50 的变化小于 2 倍(并且都在一个数量级内)。大多数差异是由于人 IYD 观察到的最大抑制或更高的化学效力所致。这种强烈的种间一致性表明,基于人类的测定法的结果将保守地预测化学物质对两栖动物 IYD 的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e1d/9887787/04519e8ed811/nihms-1849668-f0001.jpg

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