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Mol Psychiatry. 2019 Nov;24(11):1668-1684. doi: 10.1038/s41380-018-0061-1. Epub 2018 May 4.

NAD+ cellular redox and SIRT1 regulate the diurnal rhythms of tyrosine hydroxylase and conditioned cocaine reward.

Author information

1
Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh Medical School, Pittsburgh, PA, 15219, USA.
2
Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
3
Center for Systems Neurogenetics of Addiction, The Jackson Laboratory, Bar Harbor, ME, 04609, USA.
4
Center for Human Nutrition, Division of Geriatrics and Nutritional Science, Department of Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.
5
School of Medicine, Peking Union Medical College, Tsinghua University, Beijing, China.
6
Translational Neuroscience Program, Department of Psychiatry, University of Pittsburgh Medical School, Pittsburgh, PA, 15219, USA. mcclungca@upmc.edu.
7
Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, 15260, USA. mcclungca@upmc.edu.
8
Center for Systems Neurogenetics of Addiction, The Jackson Laboratory, Bar Harbor, ME, 04609, USA. mcclungca@upmc.edu.

Abstract

The diurnal regulation of dopamine is important for normal physiology and diseases such as addiction. Here we find a novel role for the CLOCK protein to antagonize CREB-mediated transcriptional activity at the tyrosine hydroxylase (TH) promoter, which is mediated by the interaction with the metabolic sensing protein, Sirtuin 1 (SIRT1). Additionally, we demonstrate that the transcriptional activity of TH is modulated by the cellular redox state, and daily rhythms of redox balance in the ventral tegmental area (VTA), along with TH transcription, are highly disrupted following chronic cocaine administration. Furthermore, CLOCK and SIRT1 are important for regulating cocaine reward and dopaminergic (DAergic) activity, with interesting differences depending on whether DAergic activity is in a heightened state and if there is a functional CLOCK protein. Taken together, we find that rhythms in cellular metabolism and circadian proteins work together to regulate dopamine synthesis and the reward value for drugs of abuse.

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