| Literature DB >> 24813609 |
Sooyoung Chung1, Eun Jeong Lee1, Seongsik Yun1, Han Kyoung Choe1, Seong-Beom Park2, Hyo Jin Son3, Kwang-Soo Kim4, Dean E Dluzen5, Inah Lee2, Onyou Hwang3, Gi Hoon Son6, Kyungjin Kim7.
Abstract
The circadian nature of mood and its dysfunction in affective disorders is well recognized, but the underlying molecular mechanisms are still unclear. Here, we show that the circadian nuclear receptor REV-ERBα, which is associated with bipolar disorder, impacts midbrain dopamine production and mood-related behavior in mice. Genetic deletion of the Rev-erbα gene or pharmacological inhibition of REV-ERBα activity in the ventral midbrain induced mania-like behavior in association with a central hyperdopaminergic state. Also, REV-ERBα repressed tyrosine hydroxylase (TH) gene transcription via competition with nuclear receptor-related 1 protein (NURR1), another nuclear receptor crucial for dopaminergic neuronal function, thereby driving circadian TH expression through a target-dependent antagonistic mechanism. In conclusion, we identified a molecular connection between the circadian timing system and mood regulation, suggesting that REV-ERBα could be targeting in the treatment of circadian rhythm-related affective disorders.Entities:
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Year: 2014 PMID: 24813609 DOI: 10.1016/j.cell.2014.03.039
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582