The function of the neurotransmitter serotonin is thought to be reduced in alcoholism. Drugs such as fluvoxamine enhance synaptic serotonin levels. Thus, these drugs were thought to be potentially useful in treating alcoholism. We have conducted studies examining whether fluvoxamine can selectively suppress ethanol-maintained behavior. We found that fluvoxamine could indeed in many circumstances selectively suppress ethanol-maintained behavior (Lamb & Jarbe, 2001; Ginsburg et al 2005). However, fluvoxamine as well as other similar drugs have not proven to be effective in treating alcoholism. In part, this is likely due to the rapid tolerance that develops to these selective effects (Ginsburg & Lamb, In Press a). However, other factors also limit the utility of fluvoxamine as well as the current utility of the procedures available for identifying new alcoholism treatment medications. This is that while fluvoxamine can selectively suppress ethanol-maintained behavior in some contexts, under other contexts this selectivity is reversed (Ginsburg & Lamb, submitted). A key to developing new effective anti-alcoholism medications is the identification of compounds that suppress ethanol-maintained behavior while leaving other important behaviors intact. Thus, it is important to understand how the experimental context can change the selectivity of potential anti-alcoholism medications and how general this context-dependent selectivity is. The two specific aims of this proposal address these questions: I) Examining the behavioral mechanisms of contextual selectivity of fluvoxamine; II) Examining the pharmacological generality of contextual selectivity. Lay Summary: Identifying the behavioral mechanisms that control pharmacological selectivity for suppressing alcohol-maintained behavior and the pharmacological generality of this effect will allow us to develop better ways of seeking new treatment medications for alcoholism, new ways of better studying alcoholism in animals, and perhaps lead to better behavioral therapies for alcoholism. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
5R01AA012337-07
Application #
7421019
Study Section
Special Emphasis Panel (ZRG1-BBBP-J (02))
Program Officer
Egli, Mark
Project Start
2001-09-24
Project End
2012-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
7
Fiscal Year
2008
Total Cost
$262,800
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Psychiatry
Type
Schools of Medicine
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Ginsburg, Brett C; Levy, Simon A; Lamb, R J (2018) Nicotine as a discriminative stimulus for ethanol use. Drug Alcohol Depend 182:98-102
Lamb, R J; Ginsburg, Brett C (2018) Addiction as a BAD, a Behavioral Allocation Disorder. Pharmacol Biochem Behav 164:62-70
Lamb, Richard J; Ginsburg, Brett C; Schindler, Charles W (2017) Conditioned Stimulus Form Does Not Explain Failures to See Pavlovian-Instrumental-Transfer With Ethanol-Paired Conditioned Stimuli. Alcohol Clin Exp Res 41:1063-1071
Lamb, R J; Schindler, Charles W; Pinkston, Jonathan W (2016) Conditioned stimuli's role in relapse: preclinical research on Pavlovian-Instrumental-Transfer. Psychopharmacology (Berl) 233:1933-44
Lamb, R J; Ginsburg, Brett C; Schindler, Charles W (2016) Effects of an ethanol-paired CS on responding for ethanol and food: Comparisons with a stimulus in a Truly-Random-Control group and to a food-paired CS on responding for food. Alcohol 57:15-27
Lamb, R J; Maguire, David R; Ginsburg, Brett C et al. (2016) Determinants of choice, and vulnerability and recovery in addiction. Behav Processes 127:35-42
Lamb, Richard J; Pinkston, Jonathan W; Ginsburg, Brett C (2015) Ethanol self-administration in mice under a second-order schedule. Alcohol 49:561-70
Lamb, Richard J; Pinkston, Jonathan W; Daws, Lynette C (2014) Ethanol effects on multiple fixed-interval, fixed-ratio responding in mice with deletions of the serotonin transporter gene. Behav Pharmacol 25:92-5
Ginsburg, Brett C; Lamb, Richard J (2014) Relative potency of varenicline or fluvoxamine to reduce responding for ethanol versus food depends on the presence or absence of concurrently earned food. Alcohol Clin Exp Res 38:860-70
Ginsburg, B C; Lamb, R J (2014) Drug effects on multiple and concurrent schedules of ethanol- and food-maintained behaviour: context-dependent selectivity. Br J Pharmacol 171:3499-510

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