Addiction is a chronic, relapsing disorder with few effective therapies. Following drug withdrawal, addicted patients experience a persistent drive to seek drugs, which is driven in part by the emergence of a negative affective state. Therapeutic strategies that could reduce this negative affective state may reduce drive for drug seeking and help prevent relapse. Two features of the withdrawal-associated negative affective state are impaired hedonic valuation of and motivation for non-drug rewards. These have both been causally linked to GABAergic and opioid-dependent interactions between the nucleus accumbens (NAc) and ventral pallidum (VP). Following withdrawal from cocaine, GABAergic transmission between the NAc and VP is weakened. This plasticity is mediated by endogenous opioids and has been causally implicated in motivational changes, hedonic valuation and cocaine seeking after withdrawal by optogenetic normalization of transmission. Since optogenetic manipulations are not applicable in clinical settings, we propose to investigate whether we can use deep brain stimulation (DBS; a surgical therapy whereby current is passed through electrodes implanted in specific brain nuclei) to restore NAc to VP transmission following cocaine withdrawal. We will first test the hypothesis that DBS in the VP can normalize transmission at NAc to VP synapses following withdrawal from cocaine self-administration. We will then test the hypothesis that DBS in the VP increases motivation for natural rewards following cocaine withdrawal. High-frequency DBS has been tested in the NAc for the treatment of addiction, although the effects have been inconsistent. Our proposal aims to improve on this approach by designing a protocol that works through well-defined synaptic mechanisms to restore circuit function after cocaine withdrawal. Moreover, understanding the principles of DBS action may have implications for treating other neuropsychiatric conditions accompanied by negative affect, such as depression or bipolar disorder.

Public Health Relevance

Addiction is a chronic, relapsing disorder which severely impacts not only the health and quality of life for patients, but also for caregivers and represents a tremendous public health and financial burden to society. Effective therapies that prevent drug relapse are therefore desperately needed. Following drug withdrawal, the emergence of a negative affective state contributes to the persistent drive to seek drugs through negative reinforcement. These persistent behavioral changes are mediated by drug-induced plasticity in the brain's reward system. By leveraging insight into how changes in neural circuits mediate this negative affect state, we will rationally design a neuromodulation protocol that can selectively reverse drug-evoked plasticity in the reward circuitry and reduce negative affect that drives subsequent drug taking and relapse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Exploratory/Developmental Grants (R21)
Project #
7R21DA047127-02
Application #
9826849
Study Section
Special Emphasis Panel (ZDA1)
Program Officer
Berton, Olivier Roland
Project Start
2018-07-01
Project End
2020-06-30
Budget Start
2018-12-01
Budget End
2019-06-30
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130