A treatment for drug addiction remains elusive due to incomplete knowledge of the brain circuits controlling both the overwhelming motivation to relapse to drug use and the ability to refrain from using drugs. In part through progress during the 20-yr tenure of this grant, we know that glutamatergic projections from cortical and allocortical brain regions to the nucleus accumbens core (NAcore) and GABAergic NAcore projections to the dorsolateral ventral pallidum (dlVP) are necessary for executing cue-induced cocaine seeking and extinction training-induced refraining from cocaine seeking. Classically, projections from the striatum contain two neuronal subtypes, those projecting to the ventral mesencephalon selectively expressing D1 dopamine receptors (D1-MSNs) and those projecting to the palldum expressing D2 receptors (D2-MSNs). Through work on this grant, we now know that NAcore D1-MSNs also innervate the dlVP1, and that activity in this D1-MSN to dlVP subcircuit is necessary for cue- induced cocaine seeking. Also, we discovered that activity in D2-MSNs is associated with extinction-induced refraining from cocaine seeking. Akin to the NAcore, the dlVP contains two primary cell types, one expressing glutamate (VPglu) and the other expressing GABA (VPGABA). Also, a subpopulation of VPGABA co-express enkephalin (VPPenk). We have begun to study the dlVP subcircuits coded by these distinct dlVP neuronal subtypes in regulating cocaine seeking and refraining from seeking. Cell-type specific chemogenetic stimulation reveals that VPglu inhibit reinstated cocaine seeking and stimulating VPPenk induces cocaine seeking. Surprisingly, VPglu and VPGABA cells in dlVP have different axon terminal fields. These findings indicate distinct roles for the different dlVP neuronal subtypes, and that divergent roles for subtype selective projections emanating from the dlVP is likely. We propose to disentangle the circuitry in which the dlVP is embedded using a combination of behavior, in vivo calcium imaging and slice electrophysiology, and test the hypothesis that VPglu activity promotes refraining during extinction responding, while VPPenk codes for cocaine seeking.

Public Health Relevance

The proposed research substantially advances our understanding of brain circuits that mediate cocaine relapse by exploring the role of newly characterized cell types. By applying innovative genetic and imaging technologies we will improve understanding of cocaine-induced neuropathology in the cell specific subcircuits regulating relapse and provide new drugable targets to inhibit relapse vulnerability.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
2R01DA012513-21
Application #
9967322
Study Section
Neurobiology of Motivated Behavior Study Section (NMB)
Program Officer
Berton, Olivier Roland
Project Start
2000-02-10
Project End
2025-03-31
Budget Start
2020-07-01
Budget End
2021-03-31
Support Year
21
Fiscal Year
2020
Total Cost
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
29407
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

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