Though drug addiction is one of the most prevalent and devastating diseases, still, relatively little is known about the molecular mechanisms that govern the long-term changes that occur in the brain that lead to addiction. It has been reported for some time that circadian rhythms are important in determining drug sensitivity and sensitization. More recently, studies have begun to emerge showing a more direct role for certain genes that make up the circadian clock in regulating not only drug-induced locomotor activity, but also the rewarding properties of drugs of abuse. This comprehensive study will examine the role of two of the primary transcription factors that make up the circadian clock, Clock and NPAS2, in regulating addiction-related behaviors. First, we will determine if cocaine (like methamphetamine) regulates the expresssion of these genes in specific regions of the brain known to be involved in drug reward. For behavioral and molecular studies, we have acquired mice that have functional knock-outs of Clock and NPAS2 and find that both mutations affect the rewarding properties of cocaine. These mice, along with mice that overexpress or knock-down these genes in specific brain regions through viral-mediated gene transfer, will be tested in a variety of behavioral paradigms to determine if mutation or overexpression of these genes leads to differences in addiction-related behaviors including self-administration, drug seeking and relapse. Finally, we will examine the molecular functions of Clock and NPAS2 to determine how they regulate two transcriptional target genes, mPerl and mPer2, that are involved in regulating drug-induced behaviors. We will determine the DMA binding at the promoters of these genes after drug exposure using gel shift analysis and ChIP, and determine if either Clock or NPAS2 are necessary to induce the Per genes after drug treatment. These studies will greatly enhance our understanding of the molecular changes that occur in the brain in response to drugs of abuse and how the circadian clock modulates drug addiction.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
1K01DA019541-01
Application #
6906974
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Satterlee, John S
Project Start
2005-04-15
Project End
2010-03-31
Budget Start
2005-04-15
Budget End
2006-03-31
Support Year
1
Fiscal Year
2005
Total Cost
$141,449
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Psychiatry
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
Falcón, Edgardo; McClung, Colleen A (2009) A role for the circadian genes in drug addiction. Neuropharmacology 56 Suppl 1:91-6
McClung, Colleen A (2007) Circadian genes, rhythms and the biology of mood disorders. Pharmacol Ther 114:222-32