. The mechanisms involved in the development of ethanol reinforcement are not fully understood. Despite the broad action of ethanol in the brain, the activation of mesolimbic dopamine (DA) neurons may represent a key systems-level process involved in goal-directed behavior and adaptive responding to the environment. Although different paradigms show that ethanol directly stimulates mesolimbic DA neurons, the involvement of DA in ethanol-reinforced behavior remains controversial. We hypothesize that (1) DA neuron activity increases transiently during ethanol self-administration and that (2) the increase is related to ethanol stimulus cues and not to ethanol action upon the DA system. The major goal of the proposed study is to distinguish DA neuron activity in real time during operant responding, during the initial phase of ethanol consumption, and later after brain ethanol has reached pharmacological levels. During these specific periods of a self-administration session, we will monitor the firing activity of multiple DA neurons in the ventral tegmental area simultaneously with multiunit recording techniques. To determine the direct pharmacological effect of ethanol on DA signaling, we will administer ethanol in freely moving rats via an intraperitoneal catheter at a rate that approximates the pharmacokinetics of ethanol during self-administration. This approach will allow us to better understand the behavioral correlates involved in the DA response during self-administration. During these procedures, we will also quantify the DA concentration in the nucleus accumbens with microdialysis to better understand the relationship between DA neuron excitability and the release of DA at the terminal regions during ethanol administration. ? ?

Public Health Relevance

. Alcohol abuse and dependence continue to cause major health and societal problems. ? However, the neuronal mechanisms that underlie this destructive behavior remain ambiguous. These experiments will provide important new insight into how brain regions that are implicated in drug addiction process information during motivated alcohol drinking. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32AA016709-01
Application #
7217153
Study Section
Special Emphasis Panel (ZAA1-HH (70))
Program Officer
Twombly, Dennis
Project Start
2006-09-30
Project End
2009-08-31
Budget Start
2006-09-30
Budget End
2007-08-31
Support Year
1
Fiscal Year
2006
Total Cost
$51,059
Indirect Cost
Name
Baylor College of Medicine
Department
Neurosciences
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Doyon, William M; Dong, Yu; Ostroumov, Alexey et al. (2013) Nicotine decreases ethanol-induced dopamine signaling and increases self-administration via stress hormones. Neuron 79:530-40