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

被引:54
作者
Bellet, Marina M. [1 ]
Vawter, Marquis P. [2 ]
Bunney, Blynn G. [2 ]
Bunney, William E. [2 ]
Sassone-Corsi, Paolo [1 ]
机构
[1] Univ Calif Irvine, Sch Med, Ctr Epigenet & Metab, Irvine, CA 92717 USA
[2] Univ Calif Irvine, Sch Med, Dept Psychiat & Human Behav, Irvine, CA 92717 USA
基金
美国国家卫生研究院;
关键词
GLYCOGEN-SYNTHASE KINASE-3-BETA; NMDA RECEPTOR ANTAGONISTS; MOLECULAR CLOCK GENES; SUPRACHIASMATIC NUCLEUS; GLUTAMATE-RECEPTOR; DEPRESSED-PATIENTS; SIGNALING PATHWAY; MOOD DISORDERS; MESSENGER-RNA; IN-VITRO;
D O I
10.1371/journal.pone.0023982
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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 GSK3 beta 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.
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页数:7
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