Proceedings of the National Academy of Sciences · 2007 · 109 citations · 32 references
Life SciencesNeurosciencePharmacologyMolecular NeuroscienceMolecular PharmacologyNeuropharmacologyAddictionAddiction NeurobiologyNeurotransmissionNicotine AddictionNicotine DependenceSynaptic TransmissionLong-term Exposure EffectsLong-term NeuroadaptationNeurobiology Of Nicotine AddictionNicotine Exposure EffectsNicotine Receptor PharmacologyNicotine Receptor SignalingNicotinic Receptor DesensitizationNicotinic Receptor Pharmacology
Chronic nicotine exposure results in long-term homeostatic regulation of nicotinic acetylcholine receptors (nAChRs) that play a key role in the adaptative cellular processes leading to addiction. However, the relative contribution of the different nAChR subunits in this process is unclear. Using genetically modified mice and pharmacological manipulations, we provide behavioral, electrophysiological, and pharmacological evidence for a long-term mechanism by which chronic nicotine triggers opposing processes differentially mediated by beta2*- vs. alpha7*nAChRs. These data offer previously undescribed insights into the understanding of nicotine addiction and the treatment of several human pathologies by nicotine-like agents chronically acting on beta2*- or alpha7*nAChRs.
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Nicotine activates and desensitizes midbrain dopamine neurons
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