Nicotine is the main addictive component of tobacco, and its behavioral and pharmacological effects are initiated by binding to neuronal nicotine acetylcholine receptors (nAChRs). Nicotine delivered by cigarette increasing the heart rate and blood pressure. The onset and duration of nicotine's peripheral effects vary. For instance, during habitual smoking, nicotine tolerance to the blood pressure effects develops faster than to the heart rate effects. Evidence suggests that the changing levels of nAChR desensitization are mechanistically linked to the development of tolerance, and desensitization and pharmacology are in turn linked to the subunit composition of the nAChRs. Although there are many in vitro studies that associated the functional properties of the receptors to their subunit composition, there are no in vivo studies that examine the systems level relationships between particular nAChR subunits and nicotine's effects. The guiding hypothesis of this proposal is that the subunit composition of nAChRs dictates the complex cardiovascular effects of nicotine, including the development of tolerance. To test our hypothesis, we will use in vivo and in vitro techniques to study mutant mice lacking nAChR subunits that are known to be expressed in the homeostasis, we will monitor blood pressure and the heart rate via radio-telemetry under basal conditions and in response to nicotine administrations. Radio-telemetry measures physiological signals and transmits them to distant receivers, thereby minimizing experimental artifacts arising from stress. The in vivo experiments will be accompanied by in vitro studies on cardiac contractility in response to nicotine and to adrenergic and cholinergic agonists. Receptor binding and in situ hybridization experiments will be conducted in collaboration with the Morphology Core to determine possible compensatory mechanisms as well as nAChR subunit up- regulation after chronic exposure to nicotine. Patch-clamp experiments in collaboration with Dr. Dani will provide information on the biophysical profile of nAChR currents in autonomic ganglia.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Program Projects (P01)
Project #
5P01DA012661-03
Application #
6464636
Study Section
Special Emphasis Panel (ZDA1)
Project Start
2001-07-01
Project End
2002-06-30
Budget Start
Budget End
Support Year
3
Fiscal Year
2001
Total Cost
$350,741
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Adriaan Bouwknecht, J; Olivier, Berend; Paylor, Richard E (2007) The stress-induced hyperthermia paradigm as a physiological animal model for anxiety: a review of pharmacological and genetic studies in the mouse. Neurosci Biobehav Rev 31:41-59
McCallum, Sarah E; Collins, Allan C; Paylor, Richard et al. (2006) Deletion of the beta 2 nicotinic acetylcholine receptor subunit alters development of tolerance to nicotine and eliminates receptor upregulation. Psychopharmacology (Berl) 184:314-27
Bao, Jianxin; Lei, Debin; Du, Yafei et al. (2005) Requirement of nicotinic acetylcholine receptor subunit beta2 in the maintenance of spiral ganglion neurons during aging. J Neurosci 25:3041-5
Armstrong, Dawna Duncan (2005) Neuropathology of Rett syndrome. J Child Neurol 20:747-53
Arredondo, Juan; Chernyavsky, Alexander I; Marubio, Lisa M et al. (2005) Receptor-mediated tobacco toxicity: regulation of gene expression through alpha3beta2 nicotinic receptor in oral epithelial cells. Am J Pathol 166:597-613
Pidoplichko, Volodymyr I; Noguchi, Jun; Areola, Oluwasanmi O et al. (2004) Nicotinic cholinergic synaptic mechanisms in the ventral tegmental area contribute to nicotine addiction. Learn Mem 11:60-9
Chernyavsky, Alex I; Arredondo, Juan; Marubio, Lisa M et al. (2004) Differential regulation of keratinocyte chemokinesis and chemotaxis through distinct nicotinic receptor subtypes. J Cell Sci 117:5665-79
Salas, Ramiro; Cook, Kimberly D; Bassetto, Laura et al. (2004) The alpha3 and beta4 nicotinic acetylcholine receptor subunits are necessary for nicotine-induced seizures and hypolocomotion in mice. Neuropharmacology 47:401-7
Tritto, Theresa; McCallum, Sarah E; Waddle, Satori A et al. (2004) Null mutant analysis of responses to nicotine: deletion of beta2 nicotinic acetylcholine receptor subunit but not alpha7 subunit reduces sensitivity to nicotine-induced locomotor depression and hypothermia. Nicotine Tob Res 6:145-58
Marubio, L M; Paylor, R (2004) Impaired passive avoidance learning in mice lacking central neuronal nicotinic acetylcholine receptors. Neuroscience 129:575-82

Showing the most recent 10 out of 34 publications