Role of the circadian nuclear receptor REV-ERBα in dorsal raphe serotonin synthesis in mood regulation

Commun Biol. 2024 Aug 15;7(1):998. doi: 10.1038/s42003-024-06647-y.

Abstract

Affective disorders are frequently associated with disrupted circadian rhythms. The existence of rhythmic secretion of central serotonin (5-hydroxytryptamine, 5-HT) pattern has been reported; however, the functional mechanism underlying the circadian control of 5-HTergic mood regulation remains largely unknown. Here, we investigate the role of the circadian nuclear receptor REV-ERBα in regulating tryptophan hydroxylase 2 (Tph2), the rate-limiting enzyme of 5-HT synthesis. We demonstrate that the REV-ERBα expressed in dorsal raphe (DR) 5-HTergic neurons functionally competes with PET-1-a nuclear activator crucial for 5-HTergic neuron development. In mice, genetic ablation of DR 5-HTergic REV-ERBα increases Tph2 expression, leading to elevated DR 5-HT levels and reduced depression-like behaviors at dusk. Further, pharmacological manipulation of the mice DR REV-ERBα activity increases DR 5-HT levels and affects despair-related behaviors. Our findings provide valuable insights into the molecular and cellular link between the circadian rhythm and the mood-controlling DR 5-HTergic systems.

MeSH terms

  • Affect / physiology
  • Animals
  • Circadian Rhythm*
  • Depression / metabolism
  • Dorsal Raphe Nucleus* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nuclear Receptor Subfamily 1, Group D, Member 1* / genetics
  • Nuclear Receptor Subfamily 1, Group D, Member 1* / metabolism
  • Serotonin* / biosynthesis
  • Serotonin* / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Tryptophan Hydroxylase* / genetics
  • Tryptophan Hydroxylase* / metabolism

Substances

  • Nuclear Receptor Subfamily 1, Group D, Member 1
  • Serotonin
  • Tryptophan Hydroxylase
  • Nr1d1 protein, mouse
  • Tph2 protein, mouse
  • Fev protein, mouse
  • Transcription Factors