Numerous studies have shown alcohol and nicotine use are correlated. Further, it has also been shown that smoking is a strong predictor for transitioning from social to problem drinking in adolescents. The reasons why alcohol and nicotine are commonly used together, however, are not completely understood and may involve multiple factors. It is possible that the co-use of alcohol with nicotine may be appealing because nicotine use during alcohol consumption may decrease some of the negative effects of alcohol such as disrupted cognition. The hippocampus is one structure involved in learning that seems particularly sensitive to the disruptive effects of ethanol. For instance, learning the context of an event, a task that is dependent on the hippocampus, is disrupted by ethanol administration in rats and mice. Preliminary findings, however, suggest that nicotine can reverse this deficit. Thus, this ability of nicotine to reduce negative effects of ethanol could facilitate greater or repeated alcohol consumption. This could facilitate a transition in drinking patterns. In addition, repeated nicotine use could also lead to nicotine addiction. It is a hypothesis of this proposal that nicotine will prevent ethanol-induced deficits in contextual conditioning in C57BL/6 mice and that the hippocampus is a neural site were nicotine works to reduce ethanol-associated learning deficits by altering the cellular processes disrupted by ethanol. As an initial step in investigating the interactive effects of nicotine on alcohol use, this proposal will examine the effects of ethanol and nicotine co-administration on hippocampus-dependent learning and also examine the neurobiology that supports ethanol-nicotine interaction. Understanding why nicotine and ethanol are co-used will aid in understanding factors that influence shifts in drinking patterns and nicotine use. Understanding the underlying neurobiology will not only further aid in this understanding but will also aid in developing treatments for alcoholism and nicotine addiction. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Small Research Grants (R03)
Project #
5R03AA015515-02
Application #
7154769
Study Section
Neurotoxicology and Alcohol Study Section (NAL)
Program Officer
Egli, Mark
Project Start
2005-12-10
Project End
2008-11-30
Budget Start
2006-12-01
Budget End
2008-11-30
Support Year
2
Fiscal Year
2007
Total Cost
$68,456
Indirect Cost
Name
Temple University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
057123192
City
Philadelphia
State
PA
Country
United States
Zip Code
19122
Gulick, Danielle; Gould, Thomas J (2011) Nicotine acts in the anterior cingulate, but not dorsal or ventral hippocampus, to reverse ethanol-induced learning impairments in the plus-maze discriminative avoidance task. Addict Biol 16:176-88
Gould, Thomas J (2010) Addiction and cognition. Addict Sci Clin Pract 5:4-14
Gulick, Danielle; Gould, Thomas J (2009) The hippocampus and cingulate cortex differentially mediate the effects of nicotine on learning versus on ethanol-induced learning deficits through different effects at nicotinic receptors. Neuropsychopharmacology 34:2167-79
Gulick, Danielle; Gould, Thomas J (2009) Interactive effects of ethanol and nicotine on learning, anxiety, and locomotion in C57BL/6 mice in the plus-maze discriminative avoidance task. Neuropharmacology 57:302-10
Gulick, Danielle; Gould, Thomas J (2009) Effects of ethanol and caffeine on behavior in C57BL/6 mice in the plus-maze discriminative avoidance task. Behav Neurosci 123:1271-8
Kenney, Justin W; Gould, Thomas J (2008) Modulation of hippocampus-dependent learning and synaptic plasticity by nicotine. Mol Neurobiol 38:101-21
Gulick, Danielle; Gould, Thomas J (2008) Interactive effects of ethanol and nicotine on learning in C57BL/6J mice depend on both dose and duration of treatment. Psychopharmacology (Berl) 196:483-95
Gulick, Danielle; Gould, Thomas J (2008) Varenicline ameliorates ethanol-induced deficits in learning in C57BL/6 mice. Neurobiol Learn Mem 90:230-6
Andre, Jessica M; Gulick, Danielle; Portugal, George S et al. (2008) Nicotine withdrawal disrupts both foreground and background contextual fear conditioning but not pre-pulse inhibition of the acoustic startle response in C57BL/6 mice. Behav Brain Res 190:174-81
Gulick, Danielle; Gould, Thomas J (2007) Acute ethanol has biphasic effects on short- and long-term memory in both foreground and background contextual fear conditioning in C57BL/6 mice. Alcohol Clin Exp Res 31:1528-37