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
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Blotting, Western
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Brain / metabolism
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CLOCK Proteins
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Circadian Rhythm
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Cocaine / pharmacology*
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Dopamine / metabolism*
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Dose-Response Relationship, Drug
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Electrophysiology
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Homozygote
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Immunohistochemistry
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Male
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Mice
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Mice, Transgenic
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Models, Neurological
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Mutation
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Neurons / metabolism
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Oligonucleotide Array Sequence Analysis
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Phenotype
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Phosphorylation
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Point Mutation
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Reward*
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Substance-Related Disorders*
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Time Factors
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Trans-Activators / genetics*
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Trans-Activators / physiology*
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Tyrosine 3-Monooxygenase / metabolism
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Ventral Tegmental Area / metabolism
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Ventral Tegmental Area / physiology*
Substances
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Trans-Activators
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Tyrosine 3-Monooxygenase
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CLOCK Proteins
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Clock protein, mouse
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Cocaine
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Dopamine