The dopaminergic (DA) synapse has been studied since the 1950s, when it was implicated in motor function, actions of antipsychotic drugs, and drug abuse. The study of DA synapses has however lagged behind that of other synapses, due to a lack of means to record dopamine release. To address this, chemical techniques have been developed, in particular electrochemical recording techniques and fluorescent false neurotransmitters (FFNs), that provide the first optical measure of neurotransmitter release from individual presynaptic sites. From these techniques, in some ways, we now know more about DA synapses than any other in the CNS. Here, we extend the contemporary understanding of DA synapses to reveal their roles in the interaction of higher organisms with the environment. This is now possible due to technical and conceptual advances, including the use of techniques novel to this proposal, including FFNs and DA-specific voltage sensors. This project tests if a) an interaction between sensory-related and reward-related excitation ?gates? local DA release, and whether this is required for normal learning and behavior; b) DA filters excitation by specific interactions with cannabinoid receptors to mediate decision-making and learning, c) learned behaviors that become established ?refine? synaptic circuits by selectively decreasing local DA activity, and that this enables future learning. The results of these experiments promise to indicate how addictive drugs such as amphetamine and opiates act to disrupt the normal operation of these steps.

Public Health Relevance

Drug abuse, psychosis in schizophrenia, attention deficit disorders, and Parkinson's disease are each caused by or treated by alterations in dopamine synaptic function: these synapses are further involved in normal learning and decision making. The precise steps by which dopamine synapses enable these functions remain unclear, but new technological advances in optical recordings have recently enabled our laboratory and others to identify specific interactions that control decisions and learning. This project will define how an animal's experience modulates dopamine synaptic activity and learning, and will help explain how addiction develops and how dopaminergic drugs treat schizophrenia, attention deficit, and Parkinson's.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
3R01DA007418-25S1
Application #
10062049
Study Section
Neurobiology of Motivated Behavior Study Section (NMB)
Program Officer
Berton, Olivier Roland
Project Start
1991-07-01
Project End
2023-11-30
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
25
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Psychiatry
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
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