Relapse to drug use during abstinence is a major challenge in the treatment of drug addiction. Both human and animal studies show that relapse is often triggered and precipitated by cues previously associated with drug self-administration. Results from rodent models of drug relapse have implicated synaptic transmission from the basolateral amygdala (BLA) to the nucleus accumbens (NAc) in cue-induced cocaine seeking. The objective of this application is to explore how BLA-to-NAc synaptic transmission is re-organized following cocaine exposure and how this re-organization contributes to cue-induced cocaine seeking. Our published and preliminary results from the last funding period suggest that the BLA-to-NAc afferent undergoes a silent synapse-based re-organization and that interfering with this re-organization attenuates cue-induced cocaine seeking. Silent synapses are thought to be immature excitatory synaptic contacts that contain NMDAR receptors (NMDARs) without stable AMPA receptors (AMPARs). By recruiting/stabilizing AMPARs, these immature synapses develop into fully functional synapses, potentially resulting in new neural circuits. Thus, generation and maturation of silent synapses in the adult brain may represent a critical and profound process of synaptic and circuitry re-organization. Based on these and other results, we hypothesize that following cocaine self-administration, nascent silent synapses are generated within the BLA-to-NAc projection, and maturation of these silent synapses critically contributes to cue-induced cocaine seeking. We will test this hypothesis in the following two aims:
Aim 1 : Characterize cocaine-induced re-organization of BLA-to-NAc synapses We will test the hypothesis that: i) the silent synapse-based synaptic re-organization within the BLA-to-NAc afferent is initiated by the formation of new presynaptic terminals and new postsynaptic partners enriched in NR2B subunit- containing NMDARs;and ii) is completed by postsynaptic insertion of calcium-permeable AMPA receptors. We will use a combination of in vivo viral tools, molecular replacement, optogenetic manipulation, and slice electrophysiology to manipulate key proteins for axonal growth/synaptogenesis, and examine the impact of these manipulations on the generation and maturation of silent synapses within the BLA-to-NAc afferent.
Aim 2 : Disrupt cocaine-induced re-organization of BLA-to-NAc synapses We will develop in vivo approaches to prevent, disrupt, or reverse cocaine-induced, silent synapse-based re-organization of the BLA- to-NAc afferent, and examine the extent to which these manipulations attenuate cocaine seeking. By accomplishing the proposed experiments, we follow an innovative conceptual angle (synaptic/circuitry re-organization) to understand the neural basis underlying cue-induced cocaine seeking. Several molecular substrates characterized in this study might be targeted experimentally and clinically for attenuating cocaine relapse. As such, this proposal is highly relevant to the mission of NIDA and NIH.

Public Health Relevance

Cue-induced cocaine seeking precipitates relapse in cocaine addicts. The proposed work will test the hypothesis that exposure to contingent environmental cues during cocaine self-administration in rats re- organizes the amygdala-to-nucleus accumbens synaptic input, likely through the generation of new synapses, which contribute to cue-induced cocaine seeking. The expected outcomes of this proposal will provide a circuitry-based understanding of cue-induced cocaine relapse and a set of targetable pharmacological substrates for clinical treatment of cocaine addiction.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
2R01DA023206-07
Application #
8367219
Study Section
Pathophysiological Basis of Mental Disorders and Addictions Study Section (PMDA)
Program Officer
Sorensen, Roger
Project Start
2007-04-01
Project End
2017-11-30
Budget Start
2013-03-01
Budget End
2013-11-30
Support Year
7
Fiscal Year
2013
Total Cost
$332,728
Indirect Cost
$112,728
Name
University of Pittsburgh
Department
Neurosciences
Type
Schools of Arts and Sciences
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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