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In vivo effects of 3-iodocytisine: pharmacological and genetic analysis of hypothermia and evaluation of chronic treatment on nicotinic binding sites.

Abstract
Several cytisine derivatives have been developed in the search for more selective drugs at nicotinic acetylcholine receptors (nAChR). Binding experiments in transfected cell lines showed that the iodination of cytisine in the position 3 of the pyridone ring increased potency at alpha7-nAChR and to a lesser extent at the alpha4beta2 subtypes, both of which are widely expressed in the brain. However, no in vivo studies have been published on this compound. Inhibition curves presented here using wild type, beta2, and beta4-null mutant mice confirm that 3-IC binds to alpha4beta2 *, alpha7 * and alpha3beta4 * receptors with higher affinity than cytisine (asterisk indicates the receptor may contain additional subunits, Lukas et al., 1999). Intraperitoneal injection of 3-iodocytisine (3-IC) induced considerable dose-dependent hypothermia in DBA/2J and C57BL/6J mice. This response was blocked by mecamylamine and partially inhibited by hexamethonium. beta4-null mice displayed significantly less 3-IC-induced hypothermia than wild-type mice, beta2-null mice were somewhat less affected than wild types, while responses of alpha7 *-null mice were similar to wild types. Mice treated chronically with 3-IC display a marked increase in alpha7 * and alpha4beta2 * binding sites determined by radioligand binding in membrane preparations from cerebral cortex and hippocampus. Quantitative autoradiographic analysis of 28 brain regions of mice treated with 3-IC was consistent with the membrane binding, detecting an increase of cytisine-sensitive [(125)I]epibatidine binding sites, while cytisine-resistant [(125)I]epibatidine sites were unchanged. [(125)I]alpha-Bungarotoxin binding sites also exhibited up-regulation. These results give a first evaluation of in vivo consequences of 3-IC as a potent agonist with marked effects on mice.
AuthorsC A Zambrano, M J Marks, B K Cassels, R B Maccioni
JournalNeuropharmacology (Neuropharmacology) Vol. 57 Issue 3 Pg. 332-42 (Sep 2009) ISSN: 1873-7064 [Electronic] England
PMID19481555 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • 3-iodocytisine
  • Alkaloids
  • Azocines
  • Chrna7 protein, mouse
  • Quinolizines
  • Receptors, Nicotinic
  • alpha7 Nicotinic Acetylcholine Receptor
  • nicotinic receptor alpha4beta2
  • nicotinic receptor subunit alpha3
Topics
  • Alkaloids (pharmacology)
  • Animals
  • Azocines (pharmacology)
  • Binding Sites
  • Brain (drug effects, metabolism)
  • Cell Membrane (drug effects, metabolism)
  • Cerebral Cortex (drug effects, metabolism)
  • Dose-Response Relationship, Drug
  • Hippocampus (drug effects, metabolism)
  • Hypothermia (chemically induced, genetics)
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Mice, Knockout
  • Quinolizines (pharmacology)
  • Random Allocation
  • Receptors, Nicotinic (genetics, metabolism)
  • alpha7 Nicotinic Acetylcholine Receptor

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