Phenotypic characterization of an alpha(4) neuronal nicotinic acetylcholine receptor subunit knock-out mouse

Citation
Sa. Ross et al., Phenotypic characterization of an alpha(4) neuronal nicotinic acetylcholine receptor subunit knock-out mouse, J NEUROSC, 20(17), 2000, pp. 6431-6441
Citations number
57
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROSCIENCE
ISSN journal
02706474 → ACNP
Volume
20
Issue
17
Year of publication
2000
Pages
6431 - 6441
Database
ISI
SICI code
0270-6474(20000901)20:17<6431:PCOAAN>2.0.ZU;2-D
Abstract
Neuronal nicotinic acetylcholine receptors (nAChR) are present in high abun dance in the nervous system (Decker et al., 1995). There are a large number of subunits expressed in the brain that combine to form multimeric functio nal receptors. We have generated an alpha(4) nAChR subunit knock-out line a nd focus on defining the behavioral role of this receptor subunit. Homozygo us mutant mice (Mt) are normal in size, fertility, and home-cage behavior. Spontaneous unconditioned motor behavior revealed an ethogram characterized by significant increases in several topographies of exploratory behavior i n Mt relative to wild-type mice (Wt) over the course of habituation to a no vel environment. Furthermore, the behavior of Mt in the elevated plus-maze assay was consistent with increased basal levels of anxiety. In response to nicotine, Wt exhibited early reductions in a number of behavioral topograp hies, under both unhabituated and habituated conditions; conversely, height ened levels of behavioral topographies in Mt were reduced by nicotine in th e late phase of the unhabituated condition. Ligand autoradiography confirme d the lack of high-affinity binding to radiolabeled nicotine, cytisine, and epibatidine in the thalamus, cortex, and caudate putamen, although binding to a number of discrete nuclei remained. The study confirms the pivotal ro le played by the alpha(4) nAChR subunit in the modulation of a number of co nstituents of the normal mouse ethogram and in anxiety as assessed using th e plus-maze. Furthermore, the response of Mt to nicotine administration sug gests that persistent nicotine binding sites in the habenulointerpeduncular system are sufficient to modulate motor activity in actively exploring mic e.