A significant population of smokers is unable or unwilling to quit smoking. As a consequence, strategies to reduce toxin exposure are being considered as a potential means of reducing tobacco-related morbidity and mortality. The purpose of this research project will be to continue to systematically examine the amount of toxin exposure across various reduction strategies and potential reduced exposure products (PREPs) using short-term, well-controlled clinical trials. In our prior TTURC project, we have focused on determining reliable and dose-responsive surrogate biomarkers for tobacco toxin exposure and risk factors for disease, and how different PREPs affect these biomarkers and the achievement of abstinence. We will expand our research efforts to better understand the underlying mechanism associated with different approaches for exposure reduction and explore factors influencing individual differences in treatment response. The focus will be on PREPs that primarily manipulate nicotine dose and closely parallels the animal studies proposed in Project 2 (Nicotine Exposure Reduction in Rats) of this TTURC. The four proposed studies involve: 1) reducing nicotine by reducing the number of cigarettes smoked; 2) reducing nicotine by reducing the nicotine yield of the cigarette smoked vs. nicotine lozenge; 3) reducing nicotine by using an antagonist treatment, nicotine vaccine; and 4) increasing nicotine by using high dose of nicotine patch with or without nicotine-free cigarettes. Subjects will be assessed at baseline, during six weeks of treatment with these products, and then during six weeks of abstinence.
The aims of the studies are to examine and compare the effects of these intervention approaches on: 1) biomarkers for tobacco toxin exposure and risk factors for disease; 2) extent of compensatory smoking, a strong determinant of toxin exposure; and 3) different aspects of tobacco addiction (e.g., physical dependence, negative affect, responses to cues, etc.). In addition, factors (genotype and phenotypes) that moderate the extent of exposure and that impact subsequent cessation will also be examined. This project, along with the TTURC projects, will provide important evidence-based data on alternative intervention methods that may potentially reduce mortality and morbidity associated with tobacco use.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Specialized Center (P50)
Project #
5P50DA013333-10
Application #
7631275
Study Section
Special Emphasis Panel (ZCA1)
Project Start
2008-06-01
Project End
2009-05-31
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
10
Fiscal Year
2008
Total Cost
$359,493
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
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Konorev, Dmitri; Koopmeiners, Joseph S; Tang, Yijin et al. (2015) Measurement of the Heterocyclic Amines 2-Amino-9H-pyrido[2,3-b]indole and 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in Urine: Effects of Cigarette Smoking. Chem Res Toxicol 28:2390-9
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Burns, Rachel J; Rothman, Alexander J; Fu, Steven S et al. (2014) The relation between social support and smoking cessation: revisiting an established measure to improve prediction. Ann Behav Med 47:369-75
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Stepanov, Irina; Knezevich, Aleksandar; Zhang, Liqin et al. (2012) Carcinogenic tobacco-specific N-nitrosamines in US cigarettes: three decades of remarkable neglect by the tobacco industry. Tob Control 21:44-8
Hecht, Stephen S; Stepanov, Irina; Hatsukami, Dorothy K (2011) Major tobacco companies have technology to reduce carcinogen levels but do not apply it to popular smokeless tobacco products. Tob Control 20:443
Harris, Andrew C; Pentel, Paul R; Burroughs, Danielle et al. (2011) A lack of association between severity of nicotine withdrawal and individual differences in compensatory nicotine self-administration in rats. Psychopharmacology (Berl) 217:153-66

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