Among the most insidious features of drug addiction is the propensity to relapse after periods of prolonged abstinence. The enduring vulnerability to relapse reflects long-term cellular changes in brain circuitry. Experiments in animal models of drug-seeking reveal adaptations in the series circuit consisting of the glutamatergic projection from the prefrontal cortex (RFC) to the nucleus accumbens and the GABA/enkephalin projection from the accumbens core (NAcore) to the ventral pallidum (VP). Identifying these projections as potentially critical in animal models of addiction has led to a search for enduring cellular changes in the PFC, NAcore and VP that underlie drug-seeking. This proposal will use a reinstatement model in rats trained to self-administer cocaine to characterize adaptations in this circuit that underlie drug-seeking. It is hypothesized that the PFC - NAcore - VP projection is a series circuit that undergoes pathological changes in protein expression and function as a result of repeated drug exposure and withdrawal. To test the veracity of this hypothesis candidate proteins will be manipulated in order to reduce cocaine- or stress-induced reinstatement of drug-seeking.
In aim #1 the role of dopamine receptor subtypes in the PFC in regulating reinstatement will be examined by a combination of drug microinjection and microdialysis.
In aims #2 and #3 the role of pre- and postsynaptic proteins that regulate glutamate transmission in the NAcore will be examined, including the cystine-glutamate exchanger, mGluR2/3, Homer and actin. A combination of microdialysis and injection of reagents to manipulate protein levels such as virus and Tat fusion proteins will be used. Finally, in the VP the role of mu opioid regulation of GABA release in drug-seeking will be characterized. The overarching goal of the proposal is to identify novel molecular targets for pharmacotherapeutic intervention in cocaine craving and relapse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA012513-08
Application #
7221268
Study Section
Neurobiology of Motivated Behavior Study Section (NMB)
Program Officer
Pilotte, Nancy S
Project Start
2000-02-10
Project End
2010-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
8
Fiscal Year
2007
Total Cost
$242,259
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
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
Neuhofer, Daniela; Kalivas, Peter (2018) Metaplasticity at the addicted tetrapartite synapse: A common denominator of drug induced adaptations and potential treatment target for addiction. Neurobiol Learn Mem 154:97-111
Bobadilla, Ana-Clara; Heinsbroek, Jasper A; Gipson, Cassandra D et al. (2017) Corticostriatal plasticity, neuronal ensembles, and regulation of drug-seeking behavior. Prog Brain Res 235:93-112
Spencer, Sade; Kalivas, Peter W (2017) Glutamate Transport: A New Bench to Bedside Mechanism for Treating Drug Abuse. Int J Neuropsychopharmacol 20:797-812
Kupchik, Yonatan M; Kalivas, Peter W (2017) The Direct and Indirect Pathways of the Nucleus Accumbens are not What You Think. Neuropsychopharmacology 42:369-370
Smith, Alexander C W; Scofield, Michael D; Heinsbroek, Jasper A et al. (2017) Accumbens nNOS Interneurons Regulate Cocaine Relapse. J Neurosci 37:742-756
Brown, Robyn Mary; Kupchik, Yonatan Michael; Spencer, Sade et al. (2017) Addiction-like Synaptic Impairments in Diet-Induced Obesity. Biol Psychiatry 81:797-806
Bobadilla, Ana-Clara; Garcia-Keller, Constanza; Heinsbroek, Jasper A et al. (2017) Accumbens Mechanisms for Cued Sucrose Seeking. Neuropsychopharmacology 42:2377-2386
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

Showing the most recent 10 out of 86 publications