|  Help  |  About  |  Contact Us

Publication : Identification of four classes of brain nicotinic receptors using beta2 mutant mice.

First Author  Zoli M Year  1998
Journal  J Neurosci Volume  18
Issue  12 Pages  4461-72
PubMed ID  9614223 Mgi Jnum  J:47985
Mgi Id  MGI:1261390 Doi  10.1523/JNEUROSCI.18-12-04461.1998
Citation  Zoli M, et al. (1998) Identification of four classes of brain nicotinic receptors using beta2 mutant mice. J Neurosci 18(12):4461-72
abstractText  Although the expression patterns of the neuronal nicotinic acetylcholine receptor (nAChR) subunits thus far described are known, the subunit composition of functional receptors in different brain areas is an ongoing question. Mice lacking the beta 2 subunit of the nAChR were used for receptor autoradiography studies and patch-clamp recording in thin brain slices. Four distinct types of nAChRs were identified, expanding on an existing classification [Alkondon M, Albuquerque EX (1993) Diversity of nicotinic acetylcholine receptors in rat hippocampal neurons. I. Pharmacological and functional evidence for distinct structural subtypes. J Pharmacol Exp Ther 265:1455-1473.], and tentatively identifying the subunit composition of nAChRs in different brain regions. Type 1 nAChRs bind alpha-bungarotoxin, are not altered in beta 2 -/- mice, and contain the alpha 7 subunit, Type 2 nAChRs contain the beta 2 subunit because they are absent in beta 2 -/- mice, bind all nicotinic agonists used with high affinity (excluding alpha-bungarotoxin), have an order of potency for nicotine >> cytisine in electrophysiological experiments, and are likely to be composed of alpha 4 beta 2 in most brain regions, with other alpha subunits contributing in specific areas. Type 3 nAChRs bind epibatidine with high affinity in equilibrium binding experiments and show that cytisine is as effective as nicotine in electrophysiological experiments; their distribution and persistence in beta 2 -/- mice strongly suggest a subunit composition of alpha 3 beta 4. Type 4 nAChRs bind cytisine and epibatidine with high affinity in equilibrium binding experiments and persist in beta 2 -/- mice; cytisine = nicotine in electrophysiological experiments. Type 4 nAChRs also exhibit faster desensitization than type 3 nAChRs at high doses of nicotine. Knock-out animals lacking individual alpha subunits should allow a further dissection of nAChR subclasses.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

5 Bio Entities

Trail: Publication

0 Expression