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Ketamine Influences CLOCK:BMAL1 Function Leading to Altered Circadian Gene Expression

机译:氯胺酮影响CLOCK:BMAL1功能,导致昼夜节律基因表达改变

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摘要

Major mood disorders have been linked to abnormalities in circadian rhythms, leading to disturbances in sleep, mood, temperature, and hormonal levels. We provide evidence that ketamine, a drug with rapid antidepressant effects, influences the function of the circadian molecular machinery. Ketamine modulates CLOCK:BMAL1-mediated transcriptional activation when these regulators are ectopically expressed in NG108-15 neuronal cells. Inhibition occurs in a dose-dependent manner and is attenuated after treatment with the GSK3β antagonist SB21673. We analyzed the effect of ketamine on circadian gene expression and observed a dose-dependent reduction in the amplitude of circadian transcription of the Bmal1, Per2, and Cry1 genes. Finally, chromatin-immunoprecipitation analyses revealed that ketamine altered the recruitment of the CLOCK:BMAL1 complex on circadian promoters in a time-dependent manner. Our results reveal a yet unsuspected molecular mode of action of ketamine and thereby may suggest possible pharmacological antidepressant strategies.
机译:主要的情绪障碍与昼夜节律异常有关,导致睡眠,情绪,温度和激素水平紊乱。我们提供的证据表明,氯胺酮是一种具有快速抗抑郁作用的药物,会影响昼夜节律分子机制的功能。当这些调节剂在NG108-15神经元细胞中异位表达时,氯胺酮调节CLOCK:BMAL1介导的转录激活。抑制作用以剂量依赖性方式发生,并在用GSK3β拮抗剂SB21673治疗后减弱。我们分析了氯胺酮对昼夜节律基因表达的影响,并观察到Bmal1,Per2和Cry1基因的昼夜节律转录幅度呈剂量依赖性降低。最后,染色质免疫沉淀分析表明,氯胺酮以时间依赖性方式改变了昼夜节律启动子上CLOCK:BMAL1复合物的募集。我们的研究结果揭示了氯胺酮的分子作用方式尚未被怀疑,因此可能暗示了可能的药理抗抑郁策略。

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