Alcoholism is a chronic, cureless, and relapsing condition. Currently, the mechanisms by which alcohol exerts its intoxicating and reinforcing effects are not completely understood, but the development of alcohol seeking, dependence, withdrawal, and even acute intoxication involve, at least in part, the actions of alcohol on neuralcircuits involving the striatum. In addition, the actions of ethanol on a number of ion channels inthe CNS have been established. Strychnine-sensitive glycine receptors (GlyRs) are among such targets of alcohol, and recent evidence demonstrates that GlyRs are expressed in forebrain regions including the striatum. Behavioral pharmacology studies suggest that GlyRs, specifically in the nucleus accumbens, are involved in alcohol consumption. However, the physiology of these particular GlyRs is not well defined, and the effects of ethanol action on native GlyRs in the striatum are not known. This project will specifically investigate GlyR physiology and ethanol pharmacology in the striatum using slice electrophysiology and molecular biology techniques. Our preliminary data suggest the presence of exogenously and tonically activated GlyR currents in the ventral striatum.
Aim 1 will characterize GlyR mediated currents and ethanol modulation of GlyR function in the striatum (dorsal and ventral) to test the hypothesis that GlyRs are important mediators of neuronal excitability and that ethanol action at GlyRs may alter striatal neuron activity.
Aim 2 will determine which GlyR subunits are involved in ethanol modulation of striatal GlyR currents using GlyR subunit knock-out (KO) mice to test the hypothesis that GlyRs containing 2 and/or 3 subunits may be particularly important for mediating the effects of striatal GlyR activation and ethanol modulation of GlyR function. Overall, findings from these experiments will provide novel insights into the effects of GlyR activation on neuronal excitabilit in the striatum and will contribute to a better understanding of how ethanol modulates striatal activity. Ultimately, by improving our knowledge of the mechanisms by which alcohol exerts its effects, new pharmacotherapies and enhanced treatment options can be developed for the treatment of alcoholism.

Public Health Relevance

Alcoholism is a chronic and relapsing medical condition with no known cure. At present the mechanisms by which alcohol produces its intoxicating and reinforcing effects are not known. By gaining a better understanding of the sites and mechanisms of action of alcohol; targets for interrupting the process of alcohol addiction can be identified; and more effective treatment options for alcohol abuse and dependence can be developed. This project focuses on the neurotransmitter substance glycine. Receptors for glycine have been identified in the brain's reward circuitry. Using animal models that lack the genes for these receptors; a role for glycine in brain activity and alcohol responses can be studied in detail.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
7F32AA022554-02
Application #
8844190
Study Section
Health Services Research Review Subcommittee (AA)
Program Officer
Cui, Changhai
Project Start
2013-09-01
Project End
2015-08-31
Budget Start
2014-05-01
Budget End
2014-08-31
Support Year
Fiscal Year
2014
Total Cost
$17,494
Indirect Cost
Name
Icahn School of Medicine at Mount Sinai
Department
Type
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029