The personal, social and criminal ramifications of psychostimulant and opioid abuse are enormous problems in North America. Clarifying the neural substrates that underlie addiction to drugs of abuse is critical for designing rational pharmacological interventions with the potential to cure addicts. A point in the cycle of addiction where pharmacological intervention can be particularly beneficial is to interfere with the overwhelming desire by addicts to use drugs. Thus, identifying the neurobiological underpinnings for engaging drug-seeking may provide novel pharmacological treatments of addiction. This proposed Neurobiology of Addiction Research Center (NARC) uses a rat model of cocaine drug-seeking behavior and unites an assemblage of investigators with expertise in behavior, neurochemistry, cell signaling and molecular biology. A core facility will generate animals having a history of stable cocaine intravenous self-administration that have been withdrawn from drug in a behavioral extinction paradigm. After various withdrawal periods, the animals will undergo a drug-primed reinstatement and be dispersed to the various projects for neurobiological evaluations. This core facility will insure consistency in experimental subjects and tissue samples amongst the projects, thereby permitting more accurate associations to be made between addiction related changes in gene expression, cell signaling, physiology, and behavior. Another aspect of the project that will be held constant is the examination of the same limbic-motor circuit that has become recognized as critical in the addiction process. Project #1 uses behavioral reinstatement to identify nuclei necessary for drug-seeking behavior that will be examined in all other projects. Project #2 will perform mRNA and protein measurements in these nuclei to identify cellular components of drug-seeking behavior. Project #3 measures monoamine transporter trafficking based in part upon findings from Projects #1 and 2. Finally, Project #4 will examine novel treatments derived from findings in the first 3 projects that possess potential for inhibiting drug-seeking behavior. In addition to this highly integrated, multi-disciplinary approach to the neurobiology and treatment of drug-seeking behavior, the NARC (via Administrative Core) will facilitate scientific interactions, provide oversight and mentor junior faculty, pre- and postdoctoral trainees and undergraduates. In part this will be accomplished through Pilot Core which will directly promote involvement of young investigators and established investigators currently outside the field of addiction to evaluate promising novel hypotheses related to the neurobiology of relapse. In summary, the NARC provides for an integrated, multidisciplinary research assault on the neurobiology of drug seeking behavior and describes a mechanism for evaluating novel pharmacological interventions. The NARC also takes advantage of the rapid growth in basic neuroscience at MUSC, as well as the existing clinical strengths in addiction research to provide a means for actively mentoring faculty and trainees.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Specialized Center (P50)
Project #
5P50DA015369-04
Application #
7068623
Study Section
Special Emphasis Panel (ZDA1-RXL-E (01))
Program Officer
Pilotte, Nancy S
Project Start
2003-08-01
Project End
2008-04-30
Budget Start
2006-05-01
Budget End
2007-04-30
Support Year
4
Fiscal Year
2006
Total Cost
$1,268,144
Indirect Cost
Name
Medical University of South Carolina
Department
Neurosciences
Type
Schools of Medicine
DUNS #
183710748
City
Charleston
State
SC
Country
United States
Zip Code
29425
Hanlon, Colleen A; Dowdle, Logan T; Gibson, Nicole B et al. (2018) Cortical substrates of cue-reactivity in multiple substance dependent populations: transdiagnostic relevance of the medial prefrontal cortex. Transl Psychiatry 8:186
Roberts-Wolfe, Douglas; Bobadilla, Ana-Clara; Heinsbroek, Jasper A et al. (2018) Drug Refraining and Seeking Potentiate Synapses on Distinct Populations of Accumbens Medium Spiny Neurons. J Neurosci 38:7100-7107
Spencer, Sade; Neuhofer, Daniela; Chioma, Vivian C et al. (2018) A Model of ?9-Tetrahydrocannabinol Self-administration and Reinstatement That Alters Synaptic Plasticity in Nucleus Accumbens. Biol Psychiatry 84:601-610
Parrilla-Carrero, Jeffrey; Buchta, William C; Goswamee, Priyodarshan et al. (2018) Restoration of Kv7 Channel-Mediated Inhibition Reduces Cued-Reinstatement of Cocaine Seeking. J Neurosci 38:4212-4229
Kearney-Ramos, Tonisha E; Lench, Daniel H; Hoffman, Michaela et al. (2018) Gray and white matter integrity influence TMS signal propagation: a multimodal evaluation in cocaine-dependent individuals. Sci Rep 8:3253
Giannotti, Giuseppe; Barry, Sarah M; Siemsen, Ben M et al. (2018) Divergent Prelimbic Cortical Pathways Interact with BDNF to Regulate Cocaine-seeking. J Neurosci 38:8956-8966
Siemsen, Ben M; Lombroso, Paul J; McGinty, Jacqueline F (2018) Intra-prelimbic cortical inhibition of striatal-enriched tyrosine phosphatase suppresses cocaine seeking in rats. Addict Biol 23:219-229
Spencer, Sade; Garcia-Keller, Constanza; Roberts-Wolfe, Douglas et al. (2017) Cocaine Use Reverses Striatal Plasticity Produced During Cocaine Seeking. Biol Psychiatry 81:616-624
Heinsbroek, Jasper A; Neuhofer, Daniela N; Griffin 3rd, William C et al. (2017) Loss of Plasticity in the D2-Accumbens Pallidal Pathway Promotes Cocaine Seeking. J Neurosci 37:757-767
Moorman, David E; James, Morgan H; Kilroy, Elisabeth A et al. (2017) Orexin/hypocretin-1 receptor antagonism reduces ethanol self-administration and reinstatement selectively in highly-motivated rats. Brain Res 1654:34-42

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