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首页> 外文期刊>Biochemical and Biophysical Research Communications >2,2,2-Trichloroethanol lengthens the circadian period of Bmal1-driven circadian bioluminescence rhythms in U2OS cells
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2,2,2-Trichloroethanol lengthens the circadian period of Bmal1-driven circadian bioluminescence rhythms in U2OS cells

机译:2,2,2-三氯乙醇延长U2OS细胞中Bmal1驱动的生物昼夜节律的生物节律周期

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摘要

2,2,2-Trichloroethanol (TCOH) is responsible for the pharmacological actions of chloral hydrate (CH), and is a major metabolite of trichloroethylene. Human exposure to TCOH is known to be increasing. Recently, it was reported that TCOH causes a significant phase delay of Per2 expression in mouse liver when injected daily over the course of several days. However, it is not clear whether TCOH directly modulates the molecular clock. In the present study we used a cell-based assay system to test this possibility. We found that the daily oscillation period of Bmal1 was lengthened to 3 h following treatment with 1.5 mM TCOH, and increased to 5 h with 3 mM TCOH treatment. However, low concentrations of TCOH had no noticeable effects. The effect of TCOH on Per2 oscillation was marginal. Interestingly, serum from rats anesthetized with CH also modulated Bmal1 period, suggesting that exposure to anesthesia should be taken into consideration for circadian rhythm studies. In summary, our study reveals a direct regulation of TCOH on molecular clock. (C) 2015 Elsevier Inc. All rights reserved.
机译:2,2,2-三氯乙醇(TCOH)负责水合氯醛(CH)的药理作用,并且是三氯乙烯的主要代谢产物。已知人类对TCOH的暴露正在增加。最近,据报道,当在几天的过程中每天注射时,TCOH在小鼠肝脏中引起Per2表达的显着相位延迟。但是,尚不清楚TCOH是否直接调节分子时钟。在本研究中,我们使用了基于细胞的分析系统来测试这种可能性。我们发现Bmal1的每日振荡周期在1.5 mM TCOH处理后延长至3 h,在3 mM TCOH处理后增加至5 h。但是,低浓度的TCOH没有明显的作用。 TCOH对Per2振荡的影响很小。有趣的是,用CH麻醉的大鼠的血清也可调节Bmal1期,这表明昼夜节律研究应考虑麻醉的暴露。总而言之,我们的研究揭示了TCOH对分子钟的直接调节。 (C)2015 Elsevier Inc.保留所有权利。

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