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SCREENING THE TOXCAST PHASE 1 CHEMICAL LIBRARY FOR INHIBITION OF DEIODINASE TYPE 1 ACTIVITY.

机译:筛选用于抑制1型脱碘酶活性的Toxcast阶段1化学文库。

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摘要

Thyroid hormone (TH) homeostasis is dependent upon coordination of multiple key events including iodide uptake, hormone synthesis, metabolism and elimination, to maintain proper TH signaling. Deiodinase enzymes catalyze iodide release from THs to interconvert THs between active and inactive forms, and are integral to hormone metabolism. The activity of deiodinases has been identified as an important endpoint to include in the context of screening chemicals for thyroid hormone disruption. To begin to address the potential for chemicals to inhibit these enzymes an adenovirus expression system was used to produce human deiodinase type 1 (DIO1) enzyme, established robust assay parameters for non-radioactive determination of iodide release by the Sandell-Kolthoff method, and employed a 96-well plate format for screening chemical libraries. An initial set of 18 chemicals was used to establish the assay, along with the known DIO1 inhibitor 6-propylthiouracil as a positive control. An additional 292 unique chemicals from the EPA’s ToxCast phase 1_v2 chemical library were screened. Chemicals were initially screened at a single high concentration of 200 μM to identify potential DIO1 inhibitors. There were 50 chemicals, or 17% of the TCp1_v2 chemicals tested, that produced >20% inhibition of DIO1 activity. Eighteen of these inhibited DIO1 activity >50% and were further tested in concentration-response mode to determine IC50s. This work presents an initial effort toward identifying chemicals with potential for affecting thyroid hormones via inhibition of deiodinases and sets the foundation for further testing of large chemical libraries against DIO1 and the other deiodinase enzymes involved in TH function.
机译:甲状腺激素(TH)稳态取决于多种关键事件的协调,包括碘化物摄取,激素合成,代谢和消除,以维持适当的TH信号传导。 Deiodinase酶催化TH释放碘化物,从而在活性和非活性形式之间相互转化TH,并且是激素代谢所必需的。脱碘酶的活性已被确定为重要的终点,包括在筛查甲状腺激素破坏的化学物质中。为了开始探讨化学物质抑制这些酶的潜力,使用腺病毒表达系统生产人类1型脱碘酶(DIO1)酶,通过Sandell-Kolthoff方法为非放射性测定碘化物的释放建立了可靠的测定参数,并采用用于筛选化学文库的96孔板格式。最初的18种化学物质与已知的DIO1抑制剂6-丙基硫氧嘧啶一起作为阳性对照,用于建立测定方法。筛选了来自EPA ToxCast 1_v2期化学库的另外292种独特的化学物质。最初以200μM的单个高浓度筛选化学物质,以鉴定潜在的DIO1抑制剂。有50种化学药品(占测试的TCp1_v2化学药品的17%)对DIO1活性的抑制作用大于20%。其中的18种抑制DIO1活性> 50%,并在浓度响应模式下进一步测试以确定IC50。这项工作提出了初步的努力,旨在通过抑制脱碘酶来鉴定具有影响甲状腺激素潜能的化学物质,并为进一步测试大型化学文库针对DIO1和其他参与TH功能的脱碘酶提供了基础。

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