Chronic exposure to tobacco smoke accounts for ~6 million deaths per year making health complications from smoking the primary cause of preventable mortality in the world. Nicotine, the addictive component of tobacco smoke, initiates dependence by binding to and activating neuronal nicotinic acetylcholine receptors (nAChRs), yet nicotine replacement therapy and existing smoking cessation aids that target abundant nAChR subtypes are minimally effective. Thus, a better understanding of neural circuits and neurotransmitter systems that contribute to nicotine withdrawal syndrome is needed to facilitate the development of new therapies for smoking cessation. Recent studies have identified the habenulo-interpeduncular (Hb-IPN) axis as a potentially important circuit that is hypothesized to mediate the aversive effects of high doses of nicotine. In addition, this pathway is involved in physical withdrawal symptoms in rodents. However, the role of the Hb-IPN circuit in affective withdrawal and the neurotransmitter systems underlying the manifestation of these symptoms are unknown. Our data indicate that the IPN may be a neuro-anatomical substrate for anxiety during nicotine withdrawal. In addition, preliminary data indicate that the stress peptide, corticotropin releasing factor (CRF), and its cognate receptors (CRF receptors) within the IPN play a significant role in nicotine withdrawal-induced anxiety in a mouse model of nicotine dependence. These observations provide the foundation for this application. We propose to test the hypothesis that chronic nicotine engages CRF signaling within the IPN, initiating the anxiogenic effects of nicotine withdrawal.
In Aim 1 we propose to use pharmacological and viral mediated gene delivery approaches to determine if CRF receptor signaling in the Hb-IPN axis is critical for the expression of anxiety during nicotine withdrawal.
In Aim 2, we will use a biophysical approach to determine how chronic nicotine and withdrawal modulates neuronal excitability within the IPN. It is anticipated that elucidating the circuitry and mechanistic detais of the anxiogenic effects of nicotine withdrawal will provide new insights into novel therapeutic strategies to facilitate smoking cessation.

Public Health Relevance

The goal of the proposed project is to identify the circuitry, brain regions, and molecular mechanisms underlying the development of anxiety during withdrawal from chronic nicotine. Ultimately, the results from this study should identify novel brain regions and molecular targets for therapies designed to alleviate affective withdrawal symptoms, thereby facilitating smoking cessation.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
1R01DA035371-01A1
Application #
8630013
Study Section
Molecular Neuropharmacology and Signaling Study Section (MNPS)
Program Officer
Sorensen, Roger
Project Start
2014-03-15
Project End
2019-02-28
Budget Start
2014-03-15
Budget End
2015-02-28
Support Year
1
Fiscal Year
2014
Total Cost
$376,312
Indirect Cost
$151,312
Name
University of Massachusetts Medical School Worcester
Department
Psychiatry
Type
Schools of Medicine
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655