Regulation of dopaminergic transmission and cocaine reward by the Clock gene

Proc Natl Acad Sci U S A. 2005 Jun 28;102(26):9377-81. doi: 10.1073/pnas.0503584102. Epub 2005 Jun 20.

Abstract

Although there are clear interactions between circadian rhythms and drug addiction, mechanisms for such interactions remain unknown. Here we establish a role for the Clock gene in regulating the brain's reward circuit. Mice lacking a functional Clock gene display an increase in cocaine reward and in the excitability of dopamine neurons in the midbrain ventral tegmental area, a key brain reward region. These phenotypes are associated with increased expression and phosphorylation of tyrosine hydroxylase (the rate-limiting enzyme in dopamine synthesis), as well as changes in several genes known to regulate dopamine activity in the ventral tegmental area. These findings demonstrate the involvement of a circadian-associated gene, Clock, in regulating dopamine function and cocaine reward.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Blotting, Western
  • Brain / metabolism
  • CLOCK Proteins
  • Circadian Rhythm
  • Cocaine / pharmacology*
  • Dopamine / metabolism*
  • Dose-Response Relationship, Drug
  • Electrophysiology
  • Homozygote
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Transgenic
  • Models, Neurological
  • Mutation
  • Neurons / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Phosphorylation
  • Point Mutation
  • Reward*
  • Substance-Related Disorders*
  • Time Factors
  • Trans-Activators / genetics*
  • Trans-Activators / physiology*
  • Tyrosine 3-Monooxygenase / metabolism
  • Ventral Tegmental Area / metabolism
  • Ventral Tegmental Area / physiology*

Substances

  • Trans-Activators
  • Tyrosine 3-Monooxygenase
  • CLOCK Proteins
  • Clock protein, mouse
  • Cocaine
  • Dopamine