Tobacco use has been implicated in a wide range of human diseases, including heart disease, emphysema, and cancer, which together result in millions of premature deaths each year. The addictive properties of nicotine are a major cause of persistent and compulsive tobacco use. Nicotine addiction is thought to result from long-term adaptive changes in the activity and expression of nicotinic acetylcholine receptors in the brain. However, the molecular and neuronal mechanisms that underlie these adaptive processes remain poorly understood. The goal of this research is to use genetic analysis in a simple animal model, the nematode Caenorhabditis elegans, to investigate the molecular basis of nicotine adaptation. C. elegans is highly amenable to molecular analysis of nervous system function: it has a simple and well characterized nervous system, and its short generation time, small and largely sequenced genome, and accessibility to germline transformation make it ideal for classical and molecular genetic studies. C. elegans exhibits a striking and easily measurable response to nicotine, and long- term nicotine exposure leads to nicotine tolerance and dependence with respect to behaviors controlled by both neuromuscular and neuronal nicotinic receptors. In this project, genes required for nicotine adaptation in nematodes will be identified by screening for adaptation-defective mutants. Two nicotine adaptation genes identified in earlier screens will be cloned to determine their molecular functions, and to characterize the cellular pathways in which they function. The possibility, suggested by studies of protein kinase C-defective mutants, that PKC phosphorylation of nicotinic receptor subunits is a mechanism for nicotine adaptation will be tested through the analysis of transgenic worms expressing mutant receptors. The ultimate goal of this work is to provide a model for the general molecular mechanisms underlying nicotine adaptation in neurons, and to identify new proteins that participate in nicotine addiction in other animals, including vertebrates.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA012891-05
Application #
6702556
Study Section
Special Emphasis Panel (ZRG1-MDCN-6 (01))
Program Officer
Satterlee, John S
Project Start
2000-02-01
Project End
2006-12-31
Budget Start
2004-01-01
Budget End
2004-12-31
Support Year
5
Fiscal Year
2004
Total Cost
$270,638
Indirect Cost
Name
University of California San Diego
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Aldrich, Melissa B; Guilliod, Renie; Fife, Caroline E et al. (2012) Lymphatic abnormalities in the normal contralateral arms of subjects with breast cancer-related lymphedema as assessed by near-infrared fluorescent imaging. Biomed Opt Express 3:1256-65
Huang, Kuang-Man; Cosman, Pamela; Schafer, William R (2008) Automated detection and analysis of foraging behavior in Caenorhabditis elegans. J Neurosci Methods 171:153-64
Kindt, Katie S; Tam, Tobey; Whiteman, Shaleah et al. (2002) Serotonin promotes G(o)-dependent neuronal migration in Caenorhabditis elegans. Curr Biol 12:1738-47
Hardaker, L A; Singer, E; Kerr, R et al. (2001) Serotonin modulates locomotory behavior and coordinates egg-laying and movement in Caenorhabditis elegans. J Neurobiol 49:303-13
Kim, J; Poole, D S; Waggoner, L E et al. (2001) Genes affecting the activity of nicotinic receptors involved in Caenorhabditis elegans egg-laying behavior. Genetics 157:1599-610