This revised application is a request for renewal of R01 DA020686. A major accomplishment of the previous funding period was identifying a key for ? 5-containing nicotinic acetylcholine receptors (?5* nAChRs) in the habenulo-interpeduncular tract in regulating nicotine intake. We found that nicotine-induced activation of ? 5* nAChRs in the habenulo-interpeduncular tract triggered a negative motivational signal that served to reduce further nicotine consumption. Genetic variation in the CHRNA5-CHRNA3-CHRNB4 gene cluster, encoding the ? 5, ? 3 and ?4 nAChR subunits respectively, increases vulnerability to tobacco addiction and smoking- associated diseases including lung cancer. Here, we will fully define the role for ? 5*, ? 3* and ? 4* nAChRs in the MHb-IPN tract regulating nicotine reinforcement.
Under Specific Aim I, we will assess nicotine self-administration behavior in knock-in mice in which the ? 5 nAChR subunit gene has been genetically modified to express a major risk allele for tobacco dependence in humans. Second, we will use an elegant combination of Double-floxed Inverted (DiO) adeno- associated viruses in Cre-expressing transgenic mice or in mice treated with Cre-expression virus to selectively re-express ? 5 nAChR subunits in discrete neuronal populations and pathways in the brains of ? 5 subunit knockout mice. We will then assess the impact on nicotine self-administration behavior in these "rescued" mice.
Under Specific Aim II we will investigate the role for ? 3* nAChRs in the habenulo-interpeduncular tract in nicotine self-administration behavior using a combination of mouse behavioral genetics and virus-mediated gene transfer in mice. Should we find that ? 3 nAChR subunits in the habenulo-interpeduncular tract regulate nicotine intake in mice we will confirm these findings by assessing the effects of virus-mediated knockdown of this subunit in the habenulo-interpeduncular tract on nicotine self-administration in rats.
Under Specific Aim III we will investigate the role for ? 4* nAChRs in the habenulo- interpeduncular tract in nicotine self-administration behavior using a combination of mouse behavioral genetics and virus-mediated gene transfer in mice. Should we find that ? 4 nAChR subunits in the habenulo-interpeduncular tract regulate nicotine intake in mice we will similarly confirm these findings by assessing the effects of virus-mediated knockdown of this subunit in the habenulo-interpeduncular tract on nicotine self-administration in rats. These studies promise to yield significantly new advances in our understanding of nicotine dependence and tobacco addiction.

Public Health Relevance

Tobacco smoking results in greater than 5 million deaths each year. Even when using the most clinically efficacious smoking cessation agents available, approximately 80% of smokers attempting to quit will relapse within one year. This highlights our need to better understand neurobiology of the nicotine dependence, which drives tobacco addiction. During the previous funding period, we found that nicotinic acetylcholine receptors (nAChRs) containing ? 5 subunits (? 5* nAChRs) in the medial habenula (MHb) and interpeduncular nucleus (IPN) served to limit nicotine consumption, and are therefore protective against tobacco addiction. In this renewal application we will significantly extend these exciting findings. This program of research promises to identify new targets for the development of therapeutic agents for smoking cessation, and may therefore have a very significant positive impact on human health.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA020686-07
Application #
8481525
Study Section
Neurobiology of Motivated Behavior Study Section (NMB)
Program Officer
Satterlee, John S
Project Start
2007-04-15
Project End
2017-03-31
Budget Start
2013-04-01
Budget End
2014-03-31
Support Year
7
Fiscal Year
2013
Total Cost
$384,912
Indirect Cost
$190,512
Name
Scripps Florida
Department
Type
DUNS #
148230662
City
Jupiter
State
FL
Country
United States
Zip Code
33458
Fowler, Christie D; Kenny, Paul J (2014) Nicotine aversion: Neurobiological mechanisms and relevance to tobacco dependence vulnerability. Neuropharmacology 76 Pt B:533-44
Kenny, Paul J; Voren, George; Johnson, Paul M (2013) Dopamine D2 receptors and striatopallidal transmission in addiction and obesity. Curr Opin Neurobiol 23:535-8
Fowler, Christie D; Tuesta, Luis; Kenny, Paul J (2013) Role of *5* nicotinic acetylcholine receptors in the effects of acute and chronic nicotine treatment on brain reward function in mice. Psychopharmacology (Berl) :
Picciotto, Marina R; Kenny, Paul J (2013) Molecular mechanisms underlying behaviors related to nicotine addiction. Cold Spring Harb Perspect Med 3:a012112
Fowler, Christie D; Kenny, Paul J (2012) Habenular signaling in nicotine reinforcement. Neuropsychopharmacology 37:306-7
Fowler, Christie D; Kenny, Paul J (2012) Utility of genetically modified mice for understanding the neurobiology of substance use disorders. Hum Genet 131:941-57
Fowler, Christie D; Kenny, Paul J (2011) Intravenous nicotine self-administration and cue-induced reinstatement in mice: effects of nicotine dose, rate of drug infusion and prior instrumental training. Neuropharmacology 61:687-98
Kenny, Paul J (2011) Tobacco dependence, the insular cortex and the hypocretin connection. Pharmacol Biochem Behav 97:700-7
Tuesta, Luis M; Fowler, Christie D; Kenny, Paul J (2011) Recent advances in understanding nicotinic receptor signaling mechanisms that regulate drug self-administration behavior. Biochem Pharmacol 82:984-95
Fowler, Christie D; Lu, Qun; Johnson, Paul M et al. (2011) Habenular ?5 nicotinic receptor subunit signalling controls nicotine intake. Nature 471:597-601

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